Cited by

This article is cited by 1744 publications

1. Zhang, T., Li, N., Wang, R., Sun, Y., He, X., Lu, X., Chu, L., & Sun, K. (2023). Enhanced therapeutic efficacy of doxorubicin against multidrug-resistant breast cancer with reduced cardiotoxicity. Drug delivery, 30(1), 2189118. https://doi.org/10.1080/10717544.2023.2189118
2. Kwantwi L. B. (2023). The dual and multifaceted role of relaxin-2 in cancer. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 10.1007/s12094-023-03146-0. Advance online publication. https://doi.org/10.1007/s12094-023-03146-0
3. Haq Khan, Z. U., Khan, T. M., Khan, A., Shah, N. S., Muhammad, N., Tahir, K., Iqbal, J., Rahim, A., Khasim, S., Ahmad, I., Shabbir, K., Gul, N. S., & Wu, J. (2023). Brief review: Applications of nanocomposite in electrochemical sensor and drugs delivery. Frontiers in chemistry, 11, 1152217. https://doi.org/10.3389/fchem.2023.1152217
4. Wang, Q., Atluri, K., Tiwari, A. K., & Babu, R. J. (2023). Exploring the Application of Micellar Drug Delivery Systems in Cancer Nanomedicine. Pharmaceuticals (Basel, Switzerland), 16(3), 433. https://doi.org/10.3390/ph16030433
5. Schröder, M., Petrova, M., Dobrikov, G. M., Grancharov, G., Momekova, D., Petrov, P. D., & Ugrinova, I. (2023). Micellar Form of a Ferrocene-Containing Camphor Sulfonamide with Improved Aqueous Solubility and Tumor Curing Potential. Pharmaceutics, 15(3), 791. https://doi.org/10.3390/pharmaceutics15030791
6. Verma, J., Warsame, C., Seenivasagam, R. K., Katiyar, N. K., Aleem, E., & Goel, S. (2023). Nanoparticle-mediated cancer cell therapy: basic science to clinical applications. Cancer metastasis reviews, 10.1007/s10555-023-10086-2. Advance online publication. https://doi.org/10.1007/s10555-023-10086-2
7. Mei, B., Lin, T. W., Sheridan, G. S., Evans, C. M., Sing, C. E., & Schweizer, K. S. (2023). How Segmental Dynamics and Mesh Confinement Determine the Selective Diffusivity of Molecules in Cross-Linked Dense Polymer Networks. ACS central science, 9(3), 508–518. https://doi.org/10.1021/acscentsci.2c01373
8. Ji, H., Lou, X., Jiao, J., Li, Y., Dai, K., & Jia, X. (2023). Preliminary Structural Characterization of Selenium Nanoparticle Composites Modified by Astragalus Polysaccharide and the Cytotoxicity Mechanism on Liver Cancer Cells. Molecules (Basel, Switzerland), 28(4), 1561. https://doi.org/10.3390/molecules28041561
9. Gostyńska, A., Czerniel, J., Kuźmińska, J., Brzozowski, J., Majchrzak-Celińska, A., Krajka-Kuźniak, V., & Stawny, M. (2023). Honokiol-Loaded Nanoemulsion for Glioblastoma Treatment: Statistical Optimization, Physicochemical Characterization, and an In Vitro Toxicity Assay. Pharmaceutics, 15(2), 448. https://doi.org/10.3390/pharmaceutics15020448
10. Josowitz, A. D., Bindra, R. S., & Saltzman, W. M. (2022). Polymer nanocarriers for targeted local delivery of agents in treating brain tumors. Nanotechnology, 34(7), 10.1088/1361-6528/ac9683. https://doi.org/10.1088/1361-6528/ac9683
11. Albert, C., Bracaglia, L., Koide, A., DiRito, J., Lysyy, T., Harkins, L., Edwards, C., Richfield, O., Grundler, J., Zhou, K., Denbaum, E., Ketavarapu, G., Hattori, T., Perincheri, S., Langford, J., Feizi, A., Haakinson, D., Hosgood, S. A., Nicholson, M. L., Pober, J. S., … Tietjen, G. T. (2022). Monobody adapter for functional antibody display on nanoparticles for adaptable targeted delivery applications. Nature communications, 13(1), 5998. https://doi.org/10.1038/s41467-022-33490-8
12. Fei, Y., Ma, Y., Zhang, H., Li, H., Feng, G., & Fang, J. (2022). Nanotechnology for research and treatment of the intestine. Journal of nanobiotechnology, 20(1), 430. https://doi.org/10.1186/s12951-022-01517-3
13. Zhang, B., Zhang, Y., Dang, W., Xing, B., Yu, C., Guo, P., Pi, J., Deng, X., Qi, D., & Liu, Z. (2022). The anti-tumor and renoprotection study of E-[c(RGDfK)2]/folic acid co-modified nanostructured lipid carrier loaded with doxorubicin hydrochloride/salvianolic acid A. Journal of nanobiotechnology, 20(1), 425. https://doi.org/10.1186/s12951-022-01628-x
14. Bozzer, S., Dal Bo, M., Grimaldi, M. C., Toffoli, G., & Macor, P. (2022). Nanocarriers as a Delivery Platform for Anticancer Treatment: Biological Limits and Perspectives in B-Cell Malignancies. Pharmaceutics, 14(9), 1965. https://doi.org/10.3390/pharmaceutics14091965
15. Cao, M., Shi, E., Wang, H., Mao, L., Wu, Q., Li, X., Liang, Y., Yang, X., Wang, Y., & Li, C. (2022). Personalized Targeted Therapeutic Strategies against Oral Squamous Cell Carcinoma. An Evidence-Based Review of Literature. International journal of nanomedicine, 17, 4293–4306. https://doi.org/10.2147/IJN.S377816
16. Sampath, G., Chen, Y. Y., Rameshkumar, N., Krishnan, M., Nagarajan, K., & Shyu, D. (2022). Biologically Synthesized Silver Nanoparticles and Their Diverse Applications. Nanomaterials (Basel, Switzerland), 12(18), 3126. https://doi.org/10.3390/nano12183126
17. Al-Numair, N. S., Theyab, A., Alzahrani, F., Shams, A. M., Al-Anazi, I. O., Oyouni, A. A. A., Al-Amer, O. M., Mavromatis, C., Saadeldin, I. M., Abdali, W. A., & Hawsawi, Y. M. (2022). Camels' biological fluids contained nanobodies: promising avenue in cancer therapy. Cancer cell international, 22(1), 279. https://doi.org/10.1186/s12935-022-02696-7
18. Sivagnanam, S., Das, K., Basak, M., Mahata, T., Stewart, A., Maity, B., & Das, P. (2022). Self-assembled dipeptide based fluorescent nanoparticles as a platform for developing cellular imaging probes and targeted drug delivery chaperones. Nanoscale advances, 4(6), 1694–1706. https://doi.org/10.1039/d1na00885d
19. Shanmugam, G., Rakshit, S., & Sarkar, K. (2022). HDAC inhibitors: Targets for tumor therapy, immune modulation and lung diseases. Translational oncology, 16, 101312. https://doi.org/10.1016/j.tranon.2021.101312
20. Lei, W., Yang, C., Wu, Y., Ru, G., He, X., Tong, X., & Wang, S. (2022). Nanocarriers surface engineered with cell membranes for cancer targeted chemotherapy. Journal of nanobiotechnology, 20(1), 45. https://doi.org/10.1186/s12951-022-01251-w
21. Wu, W., Pu, Y., & Shi, J. (2022). Nanomedicine-enabled chemotherapy-based synergetic cancer treatments. Journal of nanobiotechnology, 20(1), 4. https://doi.org/10.1186/s12951-021-01181-z
22. Xu, W. J., Cai, J. X., Li, Y. J., Wu, J. Y., & Xiang, D. (2022). Recent progress of macrophage vesicle-based drug delivery systems. Drug delivery and translational research, 10.1007/s13346-021-01110-5. Advance online publication. https://doi.org/10.1007/s13346-021-01110-5
23. Zhang, H., & Wan, L. Q. (2022). Cell Chirality as a Novel Measure for Cytotoxicity. Advanced biology, 6(1), e2101088. https://doi.org/10.1002/adbi.202101088
24. Vemuri, V. D., & Lankalapalli, S. (2021). Cocrystal Construction Between Rosuvastatin Calcium and L-asparagine with Enhanced Solubility and Dissolution Rate. Turkish journal of pharmaceutical sciences, 18(6), 790–798. https://doi.org/10.4274/tjps.galenos.2021.62333
25. Li, C., Luo, Z., Yang, L., Chen, J., Cheng, K., Xue, Y., Liu, G., Luo, X., & Wu, F. (2021). Self-assembled porphyrin polymer nanoparticles with NIR-II emission and highly efficient photothermal performance in cancer therapy. Materials today. Bio, 13, 100198. https://doi.org/10.1016/j.mtbio.2021.100198
26. Li, W., Zhang, X., Nan, Y., Jia, L., Sun, J., Zhang, L., & Wang, Y. (2021). Hyaluronidase and pH Dual-Responsive Nanoparticles for Targeted Breast Cancer Stem Cells. Frontiers in oncology, 11, 760423. https://doi.org/10.3389/fonc.2021.760423
27. Sadat, S., Wuest, M., Paiva, I. M., Munira, S., Sarrami, N., Sanaee, F., Yang, X., Paladino, M., Binkhathlan, Z., Karimi-Busheri, F., Martin, G. R., Jirik, F. R., Murray, D., Gamper, A. M., Hall, D. G., Weinfeld, M., & Lavasanifar, A. (2021). Nano-Delivery of a Novel Inhibitor of Polynucleotide Kinase/Phosphatase (PNKP) for Targeted Sensitization of Colorectal Cancer to Radiation-Induced DNA Damage. Frontiers in oncology, 11, 772920. https://doi.org/10.3389/fonc.2021.772920
28. López-Molina, S., Galiana-Roselló, C., Galiana, C., Gil-Martínez, A., Bandeira, S., & González-García, J. (2021). Alkaloids as Photosensitisers for the Inactivation of Bacteria. Antibiotics (Basel, Switzerland), 10(12), 1505. https://doi.org/10.3390/antibiotics10121505
29. Gavas, S., Quazi, S., & Karpiński, T. M. (2021). Nanoparticles for Cancer Therapy: Current Progress and Challenges. Nanoscale research letters, 16(1), 173. https://doi.org/10.1186/s11671-021-03628-6
30. Truong, N., Black, S. K., Shaw, J., Scotland, B. L., & Pearson, R. M. (2021). Microfluidic-Generated Immunomodulatory Nanoparticles and Formulation-Dependent Effects on Lipopolysaccharide-Induced Macrophage Inflammation. The AAPS journal, 24(1), 6. https://doi.org/10.1208/s12248-021-00645-2
31. Li, C., Wang, Y., Zhang, S., Zhang, J., Wang, F., Sun, Y., Huang, L., & Bian, W. (2021). pH and ROS sequentially responsive podophyllotoxin prodrug micelles with surface charge-switchable and self-amplification drug release for combating multidrug resistance cancer. Drug delivery, 28(1), 680–691. https://doi.org/10.1080/10717544.2021.1905750
32. Cabaña-Brunod, M., Herrera, P. A., Márquez-Miranda, V., Llancalahuen, F. M., Duarte, Y., González-Nilo, D., Fuentes, J. A., Vilos, C., Velásquez, L., & Otero, C. (2021). Development of a PHBV nanoparticle as a peptide vehicle for NOD1 activation. Drug delivery, 28(1), 1020–1030. https://doi.org/10.1080/10717544.2021.1923862
33. Xu, M. Q., Zhong, T., Yao, X., Li, Z. Y., Li, H., Wang, J. R., Feng, Z. H., & Zhang, X. (2021). Effect of XlogP and hansen solubility parameters on the prediction of small molecule modified docetaxel, doxorubicin and irinotecan conjugates forming stable nanoparticles. Drug delivery, 28(1), 1603–1615. https://doi.org/10.1080/10717544.2021.1958107
34. Makhani, E. Y., Zhang, A., & Haun, J. B. (2021). Quantifying and controlling bond multivalency for advanced nanoparticle targeting to cells. Nano convergence, 8(1), 38. https://doi.org/10.1186/s40580-021-00288-1
35. Adimulam, T., Arumugam, T., Foolchand, A., Ghazi, T., & Chuturgoon, A. A. (2021). The Effect of Organoselenium Compounds on Histone Deacetylase Inhibition and Their Potential for Cancer Therapy. International journal of molecular sciences, 22(23), 12952. https://doi.org/10.3390/ijms222312952
36. Mirzaei, S., Gholami, M. H., Ang, H. L., Hashemi, F., Zarrabi, A., Zabolian, A., Hushmandi, K., Delfi, M., Khan, H., Ashrafizadeh, M., Sethi, G., & Kumar, A. P. (2021). Pre-Clinical and Clinical Applications of Small Interfering RNAs (siRNA) and Co-Delivery Systems for Pancreatic Cancer Therapy. Cells, 10(12), 3348. https://doi.org/10.3390/cells10123348
37. Rabha, B., Bharadwaj, K. K., Pati, S., Choudhury, B. K., Sarkar, T., Kari, Z. A., Edinur, H. A., Baishya, D., & Atanase, L. I. (2021). Development of Polymer-Based Nanoformulations for Glioblastoma Brain Cancer Therapy and Diagnosis: An Update. Polymers, 13(23), 4114. https://doi.org/10.3390/polym13234114
38. Lv, S., Jing, R., Liu, X., Shi, H., Shi, Y., Wang, X., Zhao, X., Cao, K., & Lv, Z. (2021). One-Step Microfluidic Fabrication of Multi-Responsive Liposomes for Targeted Delivery of Doxorubicin Synergism with Photothermal Effect. International journal of nanomedicine, 16, 7759–7772. https://doi.org/10.2147/IJN.S329621
39. Kaynak, A., Davis, H. W., Vallabhapurapu, S. D., Pak, K. Y., Gray, B. D., & Qi, X. (2021). SapC-DOPS as a Novel Therapeutic and Diagnostic Agent for Glioblastoma Therapy and Detection: Alternative to Old Drugs and Agents. Pharmaceuticals (Basel, Switzerland), 14(11), 1193. https://doi.org/10.3390/ph14111193
40. Tang, C., Liu, H., Fan, Y., He, J., Li, F., Wang, J., & Hou, Y. (2021). Functional Nanomedicines for Targeted Therapy of Bladder Cancer. Frontiers in pharmacology, 12, 778973. https://doi.org/10.3389/fphar.2021.778973
41. Paca, A. M., & Ajibade, P. A. (2021). Metal Sulfide Semiconductor Nanomaterials and Polymer Microgels for Biomedical Applications. International journal of molecular sciences, 22(22), 12294. https://doi.org/10.3390/ijms222212294
42. Fraser, B., Peters, A. E., Sutherland, J. M., Liang, M., Rebourcet, D., Nixon, B., & Aitken, R. J. (2021). Biocompatible Nanomaterials as an Emerging Technology in Reproductive Health; a Focus on the Male. Frontiers in physiology, 12, 753686. https://doi.org/10.3389/fphys.2021.753686
43. Chen, W., Schilperoort, M., Cao, Y., Shi, J., Tabas, I., & Tao, W. (2021). Macrophage-targeted nanomedicine for the diagnosis and treatment of atherosclerosis. Nature reviews. Cardiology, 1–22. Advance online publication. https://doi.org/10.1038/s41569-021-00629-x
44. Singla, R. K., Sai, C. S., Chopra, H., Behzad, S., Bansal, H., Goyal, R., Gautam, R. K., Tsagkaris, C., Joon, S., Singla, S., & Shen, B. (2021). Natural Products for the Management of Castration-Resistant Prostate Cancer: Special Focus on Nanoparticles Based Studies. Frontiers in cell and developmental biology, 9, 745177. https://doi.org/10.3389/fcell.2021.745177
45. Porcheri, C., & Mitsiadis, T. A. (2021). New Scenarios in Pharmacological Treatments of Head and Neck Squamous Cell Carcinomas. Cancers, 13(21), 5515. https://doi.org/10.3390/cancers13215515
46. Li, X., Jiao, X., Li, H., & Derakhshandeh, M. (2021). Amphetamine Drug Detection with Inorganic MgO Nanotube Based on the DFT Calculations. Applied biochemistry and biotechnology, 193(11), 3528–3539. https://doi.org/10.1007/s12010-021-03633-6
47. Ganesan, K., Wang, Y., Gao, F., Liu, Q., Zhang, C., Li, P., Zhang, J., & Chen, J. (2021). Targeting Engineered Nanoparticles for Breast Cancer Therapy. Pharmaceutics, 13(11), 1829. https://doi.org/10.3390/pharmaceutics13111829
48. Xu, S., Liu, C., Zang, S., Li, J., Wang, Y., Ren, K., Li, M., Zhang, Z., & He, Q. (2021). Multifunctional self-delivery micelles targeting the invasion-metastasis cascade for enhanced chemotherapy against melanoma and the lung metastasis. Asian journal of pharmaceutical sciences, 16(6), 794–805. https://doi.org/10.1016/j.ajps.2021.08.002
49. Muñoz, R., Girotti, A., Hileeto, D., & Arias, F. J. (2021). Metronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment. Cancers, 13(21), 5414. https://doi.org/10.3390/cancers13215414
50. Xu, M. Q., Hao, Y. L., Wang, J. R., Li, Z. Y., Li, H., Feng, Z. H., Wang, H., Wang, J. W., & Zhang, X. (2021). Antitumor Activity of α-Linolenic Acid-Paclitaxel Conjugate Nanoparticles: In vitro and in vivo. International journal of nanomedicine, 16, 7269–7281. https://doi.org/10.2147/IJN.S331578
51. Rasouli, M., Fallah, N., & Bekeschus, S. (2021). Combining Nanotechnology and Gas Plasma as an Emerging Platform for Cancer Therapy: Mechanism and Therapeutic Implication. Oxidative medicine and cellular longevity, 2021, 2990326. https://doi.org/10.1155/2021/2990326
52. Raman, V., Van Dessel, N., Hall, C. L., Wetherby, V. E., Whitney, S. A., Kolewe, E. L., Bloom, S., Sharma, A., Hardy, J. A., Bollen, M., Van Eynde, A., & Forbes, N. S. (2021). Intracellular delivery of protein drugs with an autonomously lysing bacterial system reduces tumor growth and metastases. Nature communications, 12(1), 6116. https://doi.org/10.1038/s41467-021-26367-9
53. Tay, Z. W., Chandrasekharan, P., Fellows, B. D., Arrizabalaga, I. R., Yu, E., Olivo, M., & Conolly, S. M. (2021). Magnetic Particle Imaging: An Emerging Modality with Prospects in Diagnosis, Targeting and Therapy of Cancer. Cancers, 13(21), 5285. https://doi.org/10.3390/cancers13215285
54. Popova, V., Poletaeva, Y., Pyshnaya, I., Pyshnyi, D., & Dmitrienko, E. (2021). Designing pH-Dependent Systems Based on Nanoscale Calcium Carbonate for the Delivery of an Antitumor Drug. Nanomaterials (Basel, Switzerland), 11(11), 2794. https://doi.org/10.3390/nano11112794
55. Chen, X., Lee, S. K., Song, M., Zhang, T., Han, M. S., Chen, Y. T., Chen, Z., Ma, X., Tung, C. H., & Du, Y. N. (2021). RHAMMB-mediated bifunctional nanotherapy targeting Bcl-xL and mitochondria for pancreatic neuroendocrine tumor treatment. Molecular therapy oncolytics, 23, 277–287. https://doi.org/10.1016/j.omto.2021.10.002
56. Wang, H., Zheng, Y., Sun, Q., Zhang, Z., Zhao, M., Peng, C., & Shi, S. (2021). Ginsenosides emerging as both bifunctional drugs and nanocarriers for enhanced antitumor therapies. Journal of nanobiotechnology, 19(1), 322. https://doi.org/10.1186/s12951-021-01062-5
57. Loiseau, A., Boudon, J., Mirjolet, C., Morgand, V., & Millot, N. (2021). About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell Line. Nanomaterials (Basel, Switzerland), 11(10), 2733. https://doi.org/10.3390/nano11102733
58. Liu, G., Wang, M., He, H., & Li, J. (2021). Doxorubicin-Loaded Tumor-Targeting Peptide-Decorated Polypeptide Nanoparticles for Treating Primary Orthotopic Colon Cancer. Frontiers in pharmacology, 12, 744811. https://doi.org/10.3389/fphar.2021.744811
59. Mamnoon, B., Feng, L., Froberg, J., Choi, Y., Sathish, V., Taratula, O., Taratula, O., & Mallik, S. (2021). Targeting Estrogen Receptor-Positive Breast Microtumors with Endoxifen-Conjugated, Hypoxia-Sensitive Polymersomes. ACS omega, 6(42), 27654–27667. https://doi.org/10.1021/acsomega.1c02250
60. Manescu Paltanea, V., Paltanea, G., Antoniac, I., & Vasilescu, M. (2021). Magnetic Nanoparticles Used in Oncology. Materials (Basel, Switzerland), 14(20), 5948. https://doi.org/10.3390/ma14205948
61. Sano, K., Ishida, Y., Tanaka, T., Mizukami, T., Nagayama, T., Haratake, Y., Munekane, M., Yamasaki, T., & Mukai, T. (2021). Enhanced Delivery of Thermoresponsive Polymer-Based Medicine into Tumors by Using Heat Produced from Gold Nanorods Irradiated with Near-Infrared Light. Cancers, 13(19), 5005. https://doi.org/10.3390/cancers13195005
62. Long, K., Yang, Y., Lv, W., Jiang, K., Li, Y., Lo, A., Lam, W. C., Zhan, C., & Wang, W. (2021). Green Light-Triggered Intraocular Drug Release for Intravenous Chemotherapy of Retinoblastoma. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 8(20), e2101754. https://doi.org/10.1002/advs.202101754
63. Wang, X., Zhang, G., Yu, D., Wang, N., & Guan, Q. (2021). The interaction of folate-modified Bletilla striata polysaccharide-based micelle with bovine serum albumin. Glycoconjugate journal, 38(5), 585–597. https://doi.org/10.1007/s10719-021-10022-y
64. Seo, J., Do Yoo, J., Kim, M., Shim, G., Oh, Y. K., Park, R. W., Lee, B., Kim, I. S., & Kim, S. (2021). Fibrinolytic nanocages dissolve clots in the tumor microenvironment, improving the distribution and therapeutic efficacy of anticancer drugs. Experimental & molecular medicine, 53(10), 1592–1601. https://doi.org/10.1038/s12276-021-00688-7
65. Ren, L., Qiu, L., Huang, B., Yin, J., Li, Y., Yang, X., & Chen, G. (2021). Preparation and Characterization of Anti-Cancer Crystal Drugs Based on Erythrocyte Membrane Nanoplatform. Nanomaterials (Basel, Switzerland), 11(10), 2513. https://doi.org/10.3390/nano11102513
66. Dehaghani, M. Z., Yousefi, F., Seidi, F., Bagheri, B., Mashhadzadeh, A. H., Naderi, G., Esmaeili, A., Abida, O., Habibzadeh, S., Saeb, M. R., & Rybachuk, M. (2021). Encapsulation of an anticancer drug Isatin inside a host nano-vehicle SWCNT: a molecular dynamics simulation. Scientific reports, 11(1), 18753. https://doi.org/10.1038/s41598-021-98222-2
67. Claridge, B., Lozano, J., Poh, Q. H., & Greening, D. W. (2021). Development of Extracellular Vesicle Therapeutics: Challenges, Considerations, and Opportunities. Frontiers in cell and developmental biology, 9, 734720. https://doi.org/10.3389/fcell.2021.734720
68. Du, W., Gao, Y., Liu, L., Sai, S., & Ding, C. (2021). Striking Back against Fungal Infections: The Utilization of Nanosystems for Antifungal Strategies. International journal of molecular sciences, 22(18), 10104. https://doi.org/10.3390/ijms221810104
69. Zhou, Y., Lin, B., Li, K., Zhao, Y., Sun, Z., He, C., & Jha, R. K. (2021). Preparation of Near-Infrared/Photoacoustic Dual-Mode Imaging and Photothermal/Chemo Synergistic Theranostic Nanoparticles and Their Imaging and Treating of Hepatic Carcinoma. Frontiers in oncology, 11, 750807. https://doi.org/10.3389/fonc.2021.750807
70. Li, K., Li, R., Zhou, B., Chen, J., Lan, K., Zhan, W., Chen, D., Zhang, T., & Li, X. (2021). Cascade Release Nanocarriers for the Triple-Negative Breast Cancer Near-Infrared Imaging and Photothermal-Chemo Synergistic Therapy. Frontiers in oncology, 11, 747608. https://doi.org/10.3389/fonc.2021.747608
71. Ture, N., Desai, D., & Shende, P. (2021). Polyplexes of retinoic acid: an in vitro study of complex nanostructures against colorectal cancer cell line (HCT-15). Journal of materials science. Materials in medicine, 32(9), 122. https://doi.org/10.1007/s10856-021-06571-1
72. Anjum, S., Hashim, M., Malik, S. A., Khan, M., Lorenzo, J. M., Abbasi, B. H., & Hano, C. (2021). Recent Advances in Zinc Oxide Nanoparticles (ZnO NPs) for Cancer Diagnosis, Target Drug Delivery, and Treatment. Cancers, 13(18), 4570. https://doi.org/10.3390/cancers13184570
73. Ghaemi, F., Amiri, A., Bajuri, M. Y., Yuhana, N. Y., & Ferrara, M. (2021). Role of different types of nanomaterials against diagnosis, prevention and therapy of COVID-19. Sustainable cities and society, 72, 103046. https://doi.org/10.1016/j.scs.2021.103046
74. Ghose, D., Patra, C. N., Ravi Kumar, B., Swain, S., Jena, B. R., Choudhury, P., & Shree, D. (2021). QbD-based Formulation Optimization and Characterization of Polymeric Nanoparticles of Cinacalcet Hydrochloride with Improved Biopharmaceutical Attributes. Turkish journal of pharmaceutical sciences, 18(4), 452–464. https://doi.org/10.4274/tjps.galenos.2020.08522
75. Kumari, M., Krishnamurthy, P. T., Pinduprolu, S., & Sola, P. (2021). DR-5 and DLL-4 mAb Functionalized SLNs of Gamma-Secretase Inhibitors- An Approach for TNBC Treatment. Advanced pharmaceutical bulletin, 11(4), 618–623. https://doi.org/10.34172/apb.2021.070
76. Hosseinzadeh, S., Nazari, H., Esmaeili, E., & Hatamie, S. (2021). Polyethylene glycol triggers the anti-cancer impact of curcumin nanoparticles in sw-1736 thyroid cancer cells. Journal of materials science. Materials in medicine, 32(9), 112. https://doi.org/10.1007/s10856-021-06593-9
77. Bahrami, A., Arabestani, M. R., Taheri, M., Farmany, A., Zadeh, F. N., Hosseini, S. M., Nozari, H., & Nouri, F. (2021). Exploring the Role of Heavy Metals and Their Derivatives on the Pathophysiology of COVID-19. Biological trace element research, 1–12. Advance online publication. https://doi.org/10.1007/s12011-021-02893-x
78. Kim, J. H., Suh, Y. J., Park, D., Yim, H., Kim, H., Kim, H. J., Yoon, D. S., & Hwang, K. S. (2021). Technological advances in electrochemical biosensors for the detection of disease biomarkers. Biomedical engineering letters, 11(4), 1–26. Advance online publication. https://doi.org/10.1007/s13534-021-00204-w
79. de la Fuente, M., Lombardero, L., Gómez-González, A., Solari, C., Angulo-Barturen, I., Acera, A., Vecino, E., Astigarraga, E., & Barreda-Gómez, G. (2021). Enzyme Therapy: Current Challenges and Future Perspectives. International journal of molecular sciences, 22(17), 9181. https://doi.org/10.3390/ijms22179181
80. Gyanani, V., Haley, J. C., & Goswami, R. (2021). Challenges of Current Anticancer Treatment Approaches with Focus on Liposomal Drug Delivery Systems. Pharmaceuticals (Basel, Switzerland), 14(9), 835. https://doi.org/10.3390/ph14090835
81. Saladino, G. M., Kilic, N. I., Brodin, B., Hamawandi, B., Yazgan, I., Hertz, H. M., & Toprak, M. S. (2021). Carbon Quantum Dots Conjugated Rhodium Nanoparticles as Hybrid Multimodal Contrast Agents. Nanomaterials (Basel, Switzerland), 11(9), 2165. https://doi.org/10.3390/nano11092165
82. Tang, Z., Ma, Q., Chen, X., Chen, T., Ying, Y., Xi, X., Wang, L., Ma, C., Shaw, C., & Zhou, M. (2021). Recent Advances and Challenges in Nanodelivery Systems for Antimicrobial Peptides (AMPs). Antibiotics (Basel, Switzerland), 10(8), 990. https://doi.org/10.3390/antibiotics10080990
83. Pal, S., & Rakshit, T. (2021). Folate-Functionalized DNA Origami for Targeted Delivery of Doxorubicin to Triple-Negative Breast Cancer. Frontiers in chemistry, 9, 721105. https://doi.org/10.3389/fchem.2021.721105
84. Zarghami Dehaghani, M., Yousefi, F., Sajadi, S. M., Tajammal Munir, M., Abida, O., Habibzadeh, S., Mashhadzadeh, A. H., Rabiee, N., Mostafavi, E., & Saeb, M. R. (2021). Theoretical Encapsulation of Fluorouracil (5-FU) Anti-Cancer Chemotherapy Drug into Carbon Nanotubes (CNT) and Boron Nitride Nanotubes (BNNT). Molecules (Basel, Switzerland), 26(16), 4920. https://doi.org/10.3390/molecules26164920
85. Lin, Y. J., Wei, K. C., Chen, P. Y., Lim, M., & Hwang, T. L. (2021). Roles of Neutrophils in Glioma and Brain Metastases. Frontiers in immunology, 12, 701383. https://doi.org/10.3389/fimmu.2021.701383
86. Apilan, A. G., & Mothersill, C. (2021). Targeted and Non-Targeted Mechanisms for Killing Hypoxic Tumour Cells-Are There New Avenues for Treatment?. International journal of molecular sciences, 22(16), 8651. https://doi.org/10.3390/ijms22168651
87. Yuk, S. A., Kim, H., Abutaleb, N. S., Dieterly, A. M., Taha, M. S., Tsifansky, M. D., Lyle, L. T., Seleem, M. N., & Yeo, Y. (2021). Nanocapsules modify membrane interaction of polymyxin B to enable safe systemic therapy of Gram-negative sepsis. Science advances, 7(32), eabj1577. https://doi.org/10.1126/sciadv.abj1577
88. Jacoby, G., Segal Asher, M., Ehm, T., Abutbul Ionita, I., Shinar, H., Azoulay-Ginsburg, S., Zemach, I., Koren, G., Danino, D., Kozlov, M. M., Amir, R. J., & Beck, R. (2021). Order from Disorder with Intrinsically Disordered Peptide Amphiphiles. Journal of the American Chemical Society, 143(30), 11879–11888. https://doi.org/10.1021/jacs.1c06133
89. Gahan, C. G., Patel, S. J., Chen, L. M., Manson, D. E., Ehmer, Z. J., Blackwell, H. E., Van Lehn, R. C., & Lynn, D. M. (2021). Bacterial Quorum Sensing Signals Promote Large-Scale Remodeling of Lipid Membranes. Langmuir : the ACS journal of surfaces and colloids, 37(30), 9120–9136. https://doi.org/10.1021/acs.langmuir.1c01204
90. Zhang, B., Xu, Z., Zhou, W., Liu, Z., Zhao, J., & Gou, S. (2021). A light-controlled multi-step drug release nanosystem targeting tumor hypoxia for synergistic cancer therapy. Chemical science, 12(35), 11810–11820. https://doi.org/10.1039/d1sc01888d
91. Matsumura Y. (2021). Barriers to antibody therapy in solid tumors, and their solutions. Cancer science, 112(8), 2939–2947. https://doi.org/10.1111/cas.14983
92. Zhang, W., Sheng, T., Gu, Z., & Zhang, Y. (2021). Strategies for Browning Agent Delivery. Pharmaceutical research, 38(8), 1327–1334. https://doi.org/10.1007/s11095-021-03081-1
93. Lôbo, G., Paiva, K., Silva, A., Simões, M. M., Radicchi, M. A., & Báo, S. N. (2021). Nanocarriers Used in Drug Delivery to Enhance Immune System in Cancer Therapy. Pharmaceutics, 13(8), 1167. https://doi.org/10.3390/pharmaceutics13081167
94. Tang, L., Li, J., Zhao, Q., Pan, T., Zhong, H., & Wang, W. (2021). Advanced and Innovative Nano-Systems for Anticancer Targeted Drug Delivery. Pharmaceutics, 13(8), 1151. https://doi.org/10.3390/pharmaceutics13081151
95. Entzian, K., & Aigner, A. (2021). Drug Delivery by Ultrasound-Responsive Nanocarriers for Cancer Treatment. Pharmaceutics, 13(8), 1135. https://doi.org/10.3390/pharmaceutics13081135
96. Singh, D. D., & Yadav, D. K. (2021). TNBC: Potential Targeting of Multiple Receptors for a Therapeutic Breakthrough, Nanomedicine, and Immunotherapy. Biomedicines, 9(8), 876. https://doi.org/10.3390/biomedicines9080876
97. Yang, M., Zhao, H., Zhang, Z., Yuan, Q., Feng, Q., Duan, X., Wang, S., & Tang, Y. (2021). CO/light dual-activatable Ru(ii)-conjugated oligomer agent for lysosome-targeted multimodal cancer therapeutics. Chemical science, 12(34), 11515–11524. https://doi.org/10.1039/d1sc01317c
98. Ramamurthy, R., Mehta, C. H., & Nayak, U. Y. (2021). Structurally nanoengineered antimicrobial peptide polymers: design, synthesis and biomedical applications. World journal of microbiology & biotechnology, 37(8), 139. https://doi.org/10.1007/s11274-021-03109-z
99. Lin, J., Jin, J., Shen, Y., Zhang, L., Gong, G., Bian, H., Chen, H., Nagle, D. G., Wu, Y., Zhang, W., & Luan, X. (2021). Emerging protein degradation strategies: expanding the scope to extracellular and membrane proteins. Theranostics, 11(17), 8337–8349. https://doi.org/10.7150/thno.62686
100. Prajapati, R., & Somoza, Á. (2021). Albumin Nanostructures for Nucleic Acid Delivery in Cancer: Current Trend, Emerging Issues, and Possible Solutions. Cancers, 13(14), 3454. https://doi.org/10.3390/cancers13143454
101. Rasmi, Y., Saloua, K. S., Nemati, M., & Choi, J. R. (2021). Recent Progress in Nanotechnology for COVID-19 Prevention, Diagnostics and Treatment. Nanomaterials (Basel, Switzerland), 11(7), 1788. https://doi.org/10.3390/nano11071788
102. Liu, H. W., Hu, Y., Ren, Y., Nam, H., Santos, J. L., Ng, S., Gong, L., Brummet, M., Carrington, C. A., Ullman, C. G., Pomper, M. G., Minn, I., & Mao, H. Q. (2021). Scalable Purification of Plasmid DNA Nanoparticles by Tangential Flow Filtration for Systemic Delivery. ACS applied materials & interfaces, 13(26), 30326–30336. https://doi.org/10.1021/acsami.1c05750
103. van Alem, C., Metselaar, J. M., van Kooten, C., & Rotmans, J. I. (2021). Recent Advances in Liposomal-Based Anti-Inflammatory Therapy. Pharmaceutics, 13(7), 1004. https://doi.org/10.3390/pharmaceutics13071004
104. Renault-Mahieux, M., Vieillard, V., Seguin, J., Espeau, P., Le, D. T., Lai-Kuen, R., Mignet, N., Paul, M., & Andrieux, K. (2021). Co-Encapsulation of Fisetin and Cisplatin into Liposomes for Glioma Therapy: From Formulation to Cell Evaluation. Pharmaceutics, 13(7), 970. https://doi.org/10.3390/pharmaceutics13070970
105. Moradi Kashkooli, F., Soltani, M., Momeni, M. M., & Rahmim, A. (2021). Enhanced Drug Delivery to Solid Tumors via Drug-Loaded Nanocarriers: An Image-Based Computational Framework. Frontiers in oncology, 11, 655781. https://doi.org/10.3389/fonc.2021.655781
106. Liu, Z., Wu, M., Lan, M., & Zhang, W. (2021). Boosting cancer therapy efficiency via photoinduced radical production. Chemical science, 12(27), 9500–9505. https://doi.org/10.1039/d1sc01220g
107. Abu-Dahab, R., Mahmoud, N. N., Abdallah, M., Hamadneh, L., Hikmat, S., Zaza, R., Abuarqoub, D., & Khalil, E. A. (2021). Cytotoxicity and Cellular Death Modality of Surface-Decorated Gold Nanorods against a Panel of Breast Cancer Cell Lines. ACS omega, 6(24), 15903–15910. https://doi.org/10.1021/acsomega.1c01386
108. Gunaydin, G., Gedik, M. E., & Ayan, S. (2021). Photodynamic Therapy-Current Limitations and Novel Approaches. Frontiers in chemistry, 9, 691697. https://doi.org/10.3389/fchem.2021.691697
109. Musielak, M., Potoczny, J., Boś-Liedke, A., & Kozak, M. (2021). The Combination of Liposomes and Metallic Nanoparticles as Multifunctional Nanostructures in the Therapy and Medical Imaging-A Review. International journal of molecular sciences, 22(12), 6229. https://doi.org/10.3390/ijms22126229
110. Mitxelena-Iribarren, O., Lizarbe-Sancha, S., Campisi, J., Arana, S., & Mujika, M. (2021). Different Microfluidic Environments for In Vitro Testing of Lipid Nanoparticles against Osteosarcoma. Bioengineering (Basel, Switzerland), 8(6), 77. https://doi.org/10.3390/bioengineering8060077
111. Das, S., Pramanik, T., Jethwa, M., & Roy, P. (2021). Flavonoid-Decorated Nano-gold for Antimicrobial Therapy Against Gram-negative Bacteria Escherichia coli. Applied biochemistry and biotechnology, 193(6), 1727–1743. https://doi.org/10.1007/s12010-021-03543-7
112. Noor, N., Gani, A., Gani, A., Shah, A., & Ashraf, Z. U. (2021). Exploitation of polyphenols and proteins using nanoencapsulation for anti-viral and brain boosting properties - Evoking a synergistic strategy to combat COVID-19 pandemic. International journal of biological macromolecules, 180, 375–384. https://doi.org/10.1016/j.ijbiomac.2021.03.028
113. Chauhan, D. S., Dhasmana, A., Laskar, P., Prasad, R., Jain, N. K., Srivastava, R., Jaggi, M., Chauhan, S. C., & Yallapu, M. M. (2021). Nanotechnology synergized immunoengineering for cancer. European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 163, 72–101. https://doi.org/10.1016/j.ejpb.2021.03.010
114. Khodaei, M., Rostamizadeh, K., Taromchi, A. H., Monirinasab, H., & Fathi, M. (2021). DDAB cationic lipid-mPEG, PCL copolymer hybrid nano-carrier synthesis and application for delivery of siRNA targeting IGF-1R into breast cancer cells. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 23(6), 1167–1178. https://doi.org/10.1007/s12094-020-02507-3
115. Sofias, A. M., Combes, F., Koschmieder, S., Storm, G., & Lammers, T. (2021). A paradigm shift in cancer nanomedicine: from traditional tumor targeting to leveraging the immune system. Drug discovery today, 26(6), 1482–1489. https://doi.org/10.1016/j.drudis.2021.02.017
116. Chowdhury, F., Huang, B., & Wang, N. (2021). Cytoskeletal prestress: The cellular hallmark in mechanobiology and mechanomedicine. Cytoskeleton (Hoboken, N.J.), 78(6), 249–276. https://doi.org/10.1002/cm.21658
117. Rui, Y., & Green, J. J. (2021). Overcoming delivery barriers in immunotherapy for glioblastoma. Drug delivery and translational research, 1–15. Advance online publication. https://doi.org/10.1007/s13346-021-01008-2
118. Kaladharan, K., Kumar, A., Gupta, P., Illath, K., Santra, T. S., & Tseng, F. G. (2021). Microfluidic Based Physical Approaches towards Single-Cell Intracellular Delivery and Analysis. Micromachines, 12(6), 631. https://doi.org/10.3390/mi12060631
119. Zhang, F., Zhang, Y., Kong, L., Luo, H., Zhang, Y., Mäkilä, E., Salonen, J., Hirvonen, J. T., Zhu, Y., Cheng, Y., Deng, L., Zhang, H., Kros, A., Cui, W., & Santos, H. A. (2021). Multistage signal-interactive nanoparticles improve tumor targeting through efficient nanoparticle-cell communications. Cell reports, 35(8), 109131. https://doi.org/10.1016/j.celrep.2021.109131
120. Liu, Y., Zhang, B., Xu, J., Wang, X., Tang, J., & Huang, J. (2021). Phase I study of liposomal irinotecan (LY01610) in patients with advanced esophageal squamous cell carcinoma. Cancer chemotherapy and pharmacology, 1–12. Advance online publication. https://doi.org/10.1007/s00280-021-04294-2
121. Balas, M., Popescu Din, I. M., Hermenean, A., Cinteza, L. O., & Dinischiotu, A. (2021). Exposure to Iron Oxide Nanoparticles Coated with Phospholipid-Based Polymeric Micelles Induces Renal Transitory Biochemical and Histopathological Changes in Mice. Materials (Basel, Switzerland), 14(10), 2605. https://doi.org/10.3390/ma14102605
122. Ho, N. T., Siggel, M., Camacho, K. V., Bhaskara, R. M., Hicks, J. M., Yao, Y. C., Zhang, Y., Köfinger, J., Hummer, G., & Noy, A. (2021). Membrane fusion and drug delivery with carbon nanotube porins. Proceedings of the National Academy of Sciences of the United States of America, 118(19), e2016974118. https://doi.org/10.1073/pnas.2016974118
123. Yu, G., Ali, Z., Sajjad Khan, A., Ullah, K., Jamshaid, H., Zeb, A., Imran, M., Sarwar, S., Choi, H. G., & Ud Din, F. (2021). Preparation, Pharmacokinetics, and Antitumor Potential of Miltefosine-Loaded Nanostructured Lipid Carriers. International journal of nanomedicine, 16, 3255–3273. https://doi.org/10.2147/IJN.S299443
124. Ullmann, K., Leneweit, G., & Nirschl, H. (2021). How to Achieve High Encapsulation Efficiencies for Macromolecular and Sensitive APIs in Liposomes. Pharmaceutics, 13(5), 691. https://doi.org/10.3390/pharmaceutics13050691
125. Saraiva, S. M., Gutiérrez-Lovera, C., Martínez-Val, J., Lores, S., Bouzo, B. L., Díez-Villares, S., Alijas, S., Pensado-López, A., Vázquez-Ríos, A. J., Sánchez, L., & de la Fuente, M. (2021). Edelfosine nanoemulsions inhibit tumor growth of triple negative breast cancer in zebrafish xenograft model. Scientific reports, 11(1), 9873. https://doi.org/10.1038/s41598-021-87968-4
126. Moin, A., Rizvi, S., Hussain, T., Gowda, D. V., Subaiea, G. M., Elsayed, M., Ansari, M., Alanazi, A. S., & Yadav, H. (2021). Current Status of Brain Tumor in the Kingdom of Saudi Arabia and Application of Nanobiotechnology for Its Treatment: A Comprehensive Review. Life (Basel, Switzerland), 11(5), 421. https://doi.org/10.3390/life11050421
127. Vásárhelyi, L., Hegedűs, T., Sáringer, S., Ballai, G., Szilágyi, I., & Kónya, Z. (2021). Stability of Boron Nitride Nanosphere Dispersions in the Presence of Polyelectrolytes. Langmuir : the ACS journal of surfaces and colloids, 37(17), 5399–5407. https://doi.org/10.1021/acs.langmuir.1c00656
128. Ma, S., Xu, Y., & Song, W. (2021). Functional bionanomaterials for cell surface engineering in cancer immunotherapy. APL bioengineering, 5(2), 021506. https://doi.org/10.1063/5.0045945
129. Gao, P., Chang, X., Zhang, D., Cai, Y., Chen, G., Wang, H., & Wang, T. (2021). Synergistic integration of metal nanoclusters and biomolecules as hybrid systems for therapeutic applications. Acta pharmaceutica Sinica. B, 11(5), 1175–1199. https://doi.org/10.1016/j.apsb.2020.12.004
130. Naidu, E., Olojede, S. O., Lawal, S. K., Rennie, C. O., & Azu, O. O. (2021). Nanoparticle delivery system, highly active antiretroviral therapy, and testicular morphology: The role of stereology. Pharmacology research & perspectives, 9(3), e00776. https://doi.org/10.1002/prp2.776
131. Xu, Y., Guo, Y., Chen, L., Ni, D., Hu, P., & Shi, J. (2021). Tumor chemical suffocation therapy by dual respiratory inhibitions. Chemical science, 12(22), 7763–7769. https://doi.org/10.1039/d1sc00929j
132. Liao, S., Yue, W., Cai, S., Tang, Q., Lu, W., Huang, L., Qi, T., & Liao, J. (2021). Improvement of Gold Nanorods in Photothermal Therapy: Recent Progress and Perspective. Frontiers in pharmacology, 12, 664123. https://doi.org/10.3389/fphar.2021.664123
133. Li, D., Gao, C., Kuang, M., Xu, M., Wang, B., Luo, Y., Teng, L., & Xie, J. (2021). Nanoparticles as Drug Delivery Systems of RNAi in Cancer Therapy. Molecules (Basel, Switzerland), 26(8), 2380. https://doi.org/10.3390/molecules26082380
134. Lopes, R., Shi, K., Fonseca, N. A., Gama, A., Ramalho, J. S., Almeida, L., Moura, V., Simões, S., Tidor, B., & Moreira, J. N. (2021). Modelling the impact of nucleolin expression level on the activity of F3 peptide-targeted pH-sensitive pegylated liposomes containing doxorubicin. Drug delivery and translational research, 10.1007/s13346-021-00972-z. Advance online publication. https://doi.org/10.1007/s13346-021-00972-z
135. Van Gheluwe, L., Chourpa, I., Gaigne, C., & Munnier, E. (2021). Polymer-Based Smart Drug Delivery Systems for Skin Application and Demonstration of Stimuli-Responsiveness. Polymers, 13(8), 1285. https://doi.org/10.3390/polym13081285
136. Shahabadi, N., Zendehcheshm, S., & Khademi, F. (2021). Selenium nanoparticles: Synthesis, in-vitro cytotoxicity, antioxidant activity and interaction studies with ct-DNA and HSA, HHb and Cyt c serum proteins. Biotechnology reports (Amsterdam, Netherlands), 30, e00615. https://doi.org/10.1016/j.btre.2021.e00615
137. Mahmoud, B. S., & McConville, C. (2021). Development and Optimization of Irinotecan-Loaded PCL Nanoparticles and Their Cytotoxicity against Primary High-Grade Glioma Cells. Pharmaceutics, 13(4), 541. https://doi.org/10.3390/pharmaceutics13040541
138. Zhang, J. N., Xia, Y. X., & Zhang, H. J. (2021). Natural Cyclopeptides as Anticancer Agents in the Last 20 Years. International journal of molecular sciences, 22(8), 3973. https://doi.org/10.3390/ijms22083973
139. Wang, T., Suita, Y., Miriyala, S., Dean, J., Tapinos, N., & Shen, J. (2021). Advances in Lipid-Based Nanoparticles for Cancer Chemoimmunotherapy. Pharmaceutics, 13(4), 520. https://doi.org/10.3390/pharmaceutics13040520
140. Wang, S., Yu, G., Yang, W., Wang, Z., Jacobson, O., Tian, R., Deng, H., Lin, L., & Chen, X. (2021). Photodynamic-Chemodynamic Cascade Reactions for Efficient Drug Delivery and Enhanced Combination Therapy. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 8(10), 2002927. https://doi.org/10.1002/advs.202002927
141. Motiei, M., Pleno de Gouveia, L., Šopík, T., Vícha, R., Škoda, D., Císař, J., Khalili, R., Domincová Bergerová, E., Münster, L., Fei, H., Sedlařík, V., & Sáha, P. (2021). Nanoparticle-Based Rifampicin Delivery System Development. Molecules (Basel, Switzerland), 26(7), 2067. https://doi.org/10.3390/molecules26072067
142. Jia, H., Neptune, E., & Cui, H. (2021). Targeting ACE2 for COVID-19 Therapy: Opportunities and Challenges. American journal of respiratory cell and molecular biology, 64(4), 416–425. https://doi.org/10.1165/rcmb.2020-0322PS
143. Liu, X., Jiang, J., Chang, C. H., Liao, Y. P., Lodico, J. J., Tang, I., Zheng, E., Qiu, W., Lin, M., Wang, X., Ji, Y., Mei, K. C., Nel, A. E., & Meng, H. (2021). Development of Facile and Versatile Platinum Drug Delivering Silicasome Nanocarriers for Efficient Pancreatic Cancer Chemo-Immunotherapy. Small (Weinheim an der Bergstrasse, Germany), 17(14), e2005993. https://doi.org/10.1002/smll.202005993
144. Yang, Z., Zhang, L., Zhu, H., Zhou, K., Wang, H., Wang, Y., Su, R., Guo, D., Zhou, L., Xu, X., Song, P., Zheng, S., & Xie, H. (2021). Nanoparticle formulation of mycophenolate mofetil achieves enhanced efficacy against hepatocellular carcinoma by targeting tumour-associated fibroblast. Journal of cellular and molecular medicine, 25(7), 3511–3523. https://doi.org/10.1111/jcmm.16434
145. Wang, Y., Wang, J., Zhu, D., Wang, Y., Qing, G., Zhang, Y., Liu, X., & Liang, X. J. (2021). Effect of physicochemical properties on in vivo fate of nanoparticle-based cancer immunotherapies. Acta pharmaceutica Sinica. B, 11(4), 886–902. https://doi.org/10.1016/j.apsb.2021.03.007
146. Zhang, M., Hagan, C. T., 4th, Foley, H., Tian, X., Yang, F., Au, K. M., Mi, Y., Medik, Y., Roche, K., Wagner, K., Rodgers, Z., Min, Y., & Wang, A. Z. (2021). Co-delivery of etoposide and cisplatin in dual-drug loaded nanoparticles synergistically improves chemoradiotherapy in non-small cell lung cancer models. Acta biomaterialia, 124, 327–335. https://doi.org/10.1016/j.actbio.2021.02.001
147. Radmanesh, F., Sadeghi Abandansari, H., Ghanian, M. H., Pahlavan, S., Varzideh, F., Yakhkeshi, S., Alikhani, M., Moradi, S., Braun, T., & Baharvand, H. (2021). Hydrogel-mediated delivery of microRNA-92a inhibitor polyplex nanoparticles induces localized angiogenesis. Angiogenesis, 10.1007/s10456-021-09778-6. Advance online publication. https://doi.org/10.1007/s10456-021-09778-6
148. Tchounwou, P. B., Dasari, S., Noubissi, F. K., Ray, P., & Kumar, S. (2021). Advances in Our Understanding of the Molecular Mechanisms of Action of Cisplatin in Cancer Therapy. Journal of experimental pharmacology, 13, 303–328. https://doi.org/10.2147/JEP.S267383
149. Zhao, Y., He, Z., Zhang, Q., Wang, J., Jia, W., Jin, L., Zhao, L., & Lu, Y. (2021). 880 nm NIR-Triggered Organic Small Molecular-Based Nanoparticles for Photothermal Therapy of Tumor. Nanomaterials (Basel, Switzerland), 11(3), 773. https://doi.org/10.3390/nano11030773
150. Zhao, P., Qiu, L., Zhou, S., Li, L., Qian, Z., & Zhang, H. (2021). Cancer Cell Membrane Camouflaged Mesoporous Silica Nanoparticles Combined with Immune Checkpoint Blockade for Regulating Tumor Microenvironment and Enhancing Antitumor Therapy. International journal of nanomedicine, 16, 2107–2121. https://doi.org/10.2147/IJN.S295565
151. Borlan, R., Focsan, M., Maniu, D., & Astilean, S. (2021). Interventional NIR Fluorescence Imaging of Cancer: Review on Next Generation of Dye-Loaded Protein-Based Nanoparticles for Real-Time Feedback During Cancer Surgery. International journal of nanomedicine, 16, 2147–2171. https://doi.org/10.2147/IJN.S295234
152. Hingorani, D. V., Camargo, M. F., Quraishi, M. A., Adams, S. R., & Advani, S. J. (2021). Tumor Activated Cell Penetrating Peptides to Selectively Deliver Immune Modulatory Drugs. Pharmaceutics, 13(3), 365. https://doi.org/10.3390/pharmaceutics13030365
153. Luo, G., Zhang, J., Sun, Y., Wang, Y., Wang, H., Cheng, B., Shu, Q., & Fang, X. (2021). Nanoplatforms for Sepsis Management: Rapid Detection/Warning, Pathogen Elimination and Restoring Immune Homeostasis. Nano-micro letters, 13, 88. https://doi.org/10.1007/s40820-021-00598-3
154. Jiang, Q., Liu, L., Li, Q., Cao, Y., Chen, D., Du, Q., Yang, X., Huang, D., Pei, R., Chen, X., & Huang, G. (2021). NIR-laser-triggered gadolinium-doped carbon dots for magnetic resonance imaging, drug delivery and combined photothermal chemotherapy for triple negative breast cancer. Journal of nanobiotechnology, 19(1), 64. https://doi.org/10.1186/s12951-021-00811-w
155. Rodell, C. B., Baldwin, P., Fernandez, B., Weissleder, R., Sridhar, S., & Dubach, J. M. (2021). Quantification of Cellular Drug Biodistribution Addresses Challenges in Evaluating in vitro and in vivo Encapsulated Drug Delivery. Advanced therapeutics, 4(3), 2000125. https://doi.org/10.1002/adtp.202000125
156. Tsai, L. H., Yen, C. H., Hsieh, H. Y., & Young, T. H. (2021). Doxorubicin Loaded PLGA Nanoparticle with Cationic/Anionic Polyelectrolyte Decoration: Characterization, and Its Therapeutic Potency. Polymers, 13(5), 693. https://doi.org/10.3390/polym13050693
157. Nabil, G., Alzhrani, R., Alsaab, H. O., Atef, M., Sau, S., Iyer, A. K., & Banna, H. E. (2021). CD44 Targeted Nanomaterials for Treatment of Triple-Negative Breast Cancer. Cancers, 13(4), 898. https://doi.org/10.3390/cancers13040898
158. Pritchard, N., Kaitu'u-Lino, T., Harris, L., Tong, S., & Hannan, N. (2021). Nanoparticles in pregnancy: the next frontier in reproductive therapeutics. Human reproduction update, 27(2), 280–304. https://doi.org/10.1093/humupd/dmaa049
159. Khan, A. A., & T M de Rosales, R. (2021). Radiolabelling of Extracellular Vesicles for PET and SPECT imaging. Nanotheranostics, 5(3), 256–274. https://doi.org/10.7150/ntno.51676
160. Izci, M., Maksoudian, C., Manshian, B. B., & Soenen, S. J. (2021). The Use of Alternative Strategies for Enhanced Nanoparticle Delivery to Solid Tumors. Chemical reviews, 121(3), 1746–1803. https://doi.org/10.1021/acs.chemrev.0c00779
161. Jiang, Y., Huang, J., Xu, C., & Pu, K. (2021). Activatable polymer nanoagonist for second near-infrared photothermal immunotherapy of cancer. Nature communications, 12(1), 742. https://doi.org/10.1038/s41467-021-21047-0
162. Thambiraj, S., Vijayalakshmi, R., & Ravi Shankaran, D. (2021). An effective strategy for development of docetaxel encapsulated gold nanoformulations for treatment of prostate cancer. Scientific reports, 11(1), 2808. https://doi.org/10.1038/s41598-020-80529-1
163. Aramini, B., Masciale, V., Grisendi, G., Banchelli, F., D'Amico, R., Maiorana, A., Morandi, U., Dominici, M., & Haider, K. H. (2021). Cancer stem cells and macrophages: molecular connections and future perspectives against cancer. Oncotarget, 12(3), 230–250. https://doi.org/10.18632/oncotarget.27870
164. Qiu, J., Xu, J., & Xia, Y. (2021). Nanobottles for Controlled Release and Drug Delivery. Advanced healthcare materials, 10(4), e2000587. https://doi.org/10.1002/adhm.202000587
165. Shinn, J., Lee, S., Lee, H. K., Ahn, J., Lee, S. A., Lee, S., & Lee, Y. (2021). Recent progress in development and applications of second near-infrared (NIR-II) nanoprobes. Archives of pharmacal research, 44(2), 165–181. https://doi.org/10.1007/s12272-021-01313-x
166. Kurzątkowska, K., Pazos, M. A., 2nd, Herschkowitz, J. I., & Hepel, M. (2021). Cancer-Targeted Controlled Delivery of Chemotherapeutic Anthracycline Derivatives Using Apoferritin Nanocage Carriers. International journal of molecular sciences, 22(3), 1362. https://doi.org/10.3390/ijms22031362
167. Khan, A., Dias, F., Neekhra, S., Singh, B., & Srivastava, R. (2021). Designing and Immunomodulating Multiresponsive Nanomaterial for Cancer Theranostics. Frontiers in chemistry, 8, 631351. https://doi.org/10.3389/fchem.2020.631351
168. Zhou, X., Liu, X., & Huang, L. (2021). Macrophage-Mediated Tumor Cell Phagocytosis: Opportunity for Nanomedicine Intervention. Advanced functional materials, 31(5), 2006220. https://doi.org/10.1002/adfm.202006220
169. Kanduč, M., Kim, W. K., Roa, R., & Dzubiella, J. (2021). How the Shape and Chemistry of Molecular Penetrants Control Responsive Hydrogel Permeability. ACS nano, 15(1), 614–624. https://doi.org/10.1021/acsnano.0c06319
170. Jahan, S., Karim, M. E., & Chowdhury, E. H. (2021). Nanoparticles Targeting Receptors on Breast Cancer for Efficient Delivery of Chemotherapeutics. Biomedicines, 9(2), 114. https://doi.org/10.3390/biomedicines9020114
171. Yau, A., Lee, J., & Chen, Y. (2021). Nanomaterials for Protein Delivery in Anticancer Applications. Pharmaceutics, 13(2), 155. https://doi.org/10.3390/pharmaceutics13020155
172. AbouAitah, K., & Lojkowski, W. (2021). Delivery of Natural Agents by Means of Mesoporous Silica Nanospheres as a Promising Anticancer Strategy. Pharmaceutics, 13(2), 143. https://doi.org/10.3390/pharmaceutics13020143
173. Graham, M., & Shchukin, D. (2021). Formation Mechanism of Multipurpose Silica Nanocapsules. Langmuir : the ACS journal of surfaces and colloids, 37(2), 918–927. https://doi.org/10.1021/acs.langmuir.0c03286
174. Fakih, H. H., Katolik, A., Malek-Adamian, E., Fakhoury, J. J., Kaviani, S., Damha, M. J., & Sleiman, H. F. (2021). Design and enhanced gene silencing activity of spherical 2'-fluoroarabinose nucleic acids (FANA-SNAs). Chemical science, 12(8), 2993–3003. https://doi.org/10.1039/d0sc06645a
175. Andrade-Gagnon, B., Bélanger-Bouliga, M., Trang Nguyen, P., Nguyen, T., Bourgault, S., & Nazemi, A. (2021). Degradable Spirocyclic Polyacetal-Based Core-Amphiphilic Assemblies for Encapsulation and Release of Hydrophobic Cargo. Nanomaterials (Basel, Switzerland), 11(1), 161. https://doi.org/10.3390/nano11010161
176. Albalawi, F., Hussein, M. Z., Fakurazi, S., & Masarudin, M. J. (2021). Engineered Nanomaterials: The Challenges and Opportunities for Nanomedicines. International journal of nanomedicine, 16, 161–184. https://doi.org/10.2147/IJN.S288236
177. Wang, P., Yan, G., Zhu, X., Du, Y., Chen, D., & Zhang, J. (2021). Heterofullerene MC59 (M = B, Si, Al) as Potential Carriers for Hydroxyurea Drug Delivery. Nanomaterials (Basel, Switzerland), 11(1), 115. https://doi.org/10.3390/nano11010115
178. Zhang, L., Mu, C., Zhang, T., Yang, D., Wang, C., Chen, Q., Tang, L., Fan, L., Liu, C., Shen, J., & Li, H. (2021). Development of targeted therapy therapeutics to sensitize triple-negative breast cancer chemosensitivity utilizing bacteriophage phi29 derived packaging RNA. Journal of nanobiotechnology, 19(1), 13. https://doi.org/10.1186/s12951-020-00758-4
179. El-Sahli, S., Hua, K., Sulaiman, A., Chambers, J., Li, L., Farah, E., McGarry, S., Liu, D., Zheng, P., Lee, S. H., Cui, J., Ekker, M., Côté, M., Alain, T., Li, X., D'Costa, V. M., Wang, L., & Gadde, S. (2021). A triple-drug nanotherapy to target breast cancer cells, cancer stem cells, and tumor vasculature. Cell death & disease, 12(1), 8. https://doi.org/10.1038/s41419-020-03308-w
180. Gregoriou, Y., Gregoriou, G., Yilmaz, V., Kapnisis, K., Prokopi, M., Anayiotos, A., Strati, K., Dietis, N., Constantinou, A. I., & Andreou, C. (2021). Resveratrol loaded polymeric micelles for theranostic targeting of breast cancer cells. Nanotheranostics, 5(1), 113–124. https://doi.org/10.7150/ntno.51955
181. Bauleth-Ramos, T., & Sarmento, B. (2021). In Vitro Assays for Nanoparticle-Cancer Cell Interaction Studies. Advances in experimental medicine and biology, 1295, 223–242. https://doi.org/10.1007/978-3-030-58174-9_10
182. Grimaudo M. A. (2021). Nanotechnology for the Development of Nanovaccines in Cancer Immunotherapy. Advances in experimental medicine and biology, 1295, 303–315. https://doi.org/10.1007/978-3-030-58174-9_13
183. Li, M., Qin, M., Song, G., Deng, H., Wang, D., Wang, X., Dai, W., He, B., Zhang, H., & Zhang, Q. (2021). A biomimetic antitumor nanovaccine based on biocompatible calcium pyrophosphate and tumor cell membrane antigens. Asian journal of pharmaceutical sciences, 16(1), 97–109. https://doi.org/10.1016/j.ajps.2020.06.006
184. Joo J. (2021). Diagnostic and Therapeutic Nanomedicine. Advances in experimental medicine and biology, 1310, 401–447. https://doi.org/10.1007/978-981-33-6064-8_15
185. Saw, P. E., Xu, X., Kang, B. R., Lee, J., Lee, Y. S., Kim, C., Kim, H., Kang, S. H., Na, Y. J., Moon, H. J., Kim, J. H., Park, Y. K., Yoon, W., Kim, J. H., Kwon, T. H., Choi, C., Jon, S., & Chong, K. (2021). Extra-domain B of fibronectin as an alternative target for drug delivery and a cancer diagnostic and prognostic biomarker for malignant glioma. Theranostics, 11(2), 941–957. https://doi.org/10.7150/thno.44948
186. Meng, B., Strawbridge, R. R., Tichauer, K., Samkoe, K. S., & Davis, S. C. (2021). Monitoring cancer cell surface receptor expression during anti-angiogenesis therapy in vivo. Proceedings of SPIE--the International Society for Optical Engineering, 11625, 116250Q.
187. Decuzzi, P., Peer, D., Mascolo, D. D., Palange, A. L., Manghnani, P. N., Moghimi, S. M., Farhangrazi, Z. S., Howard, K. A., Rosenblum, D., Liang, T., Chen, Z., Wang, Z., Zhu, J. J., Gu, Z., Korin, N., Letourneur, D., Chauvierre, C., van der Meel, R., Kiessling, F., & Lammers, T. (2021). Roadmap on nanomedicine. Nanotechnology, 32(1), 012001. https://doi.org/10.1088/1361-6528/abaadb
188. Beyaz, H., Uludag, H., Kavaz, D., & Rizaner, N. (2021). Mechanisms of Drug Resistance and Use of Nanoparticle Delivery to Overcome Resistance in Breast Cancers. Advances in experimental medicine and biology, 1347, 163–181. https://doi.org/10.1007/5584_2021_648
189. Tawfik, S. M., Azizov, S., Elmasry, M. R., Sharipov, M., & Lee, Y. I. (2020). Recent Advances in Nanomicelles Delivery Systems. Nanomaterials (Basel, Switzerland), 11(1), 70. https://doi.org/10.3390/nano11010070
190. Volpi, S., Cancelli, U., Neri, M., & Corradini, R. (2020). Multifunctional Delivery Systems for Peptide Nucleic Acids. Pharmaceuticals (Basel, Switzerland), 14(1), 14. https://doi.org/10.3390/ph14010014
191. Ros, C., Bieri, J., & Leisi, R. (2020). The VP1u of Human Parvovirus B19: A Multifunctional Capsid Protein with Biotechnological Applications. Viruses, 12(12), 1463. https://doi.org/10.3390/v12121463
192. Kvetkina, A., Malyarenko, O., Pavlenko, A., Dyshlovoy, S., von Amsberg, G., Ermakova, S., & Leychenko, E. (2020). Sea Anemone Heteractis crispa Actinoporin Demonstrates In Vitro Anticancer Activities and Prevents HT-29 Colorectal Cancer Cell Migration. Molecules (Basel, Switzerland), 25(24), 5979. https://doi.org/10.3390/molecules25245979
193. Juszkiewicz, K., Sikorski, A. F., & Czogalla, A. (2020). Building Blocks to Design Liposomal Delivery Systems. International journal of molecular sciences, 21(24), 9559. https://doi.org/10.3390/ijms21249559
194. Mamidi, N., Velasco Delgadillo, R. M., Gonzáles Ortiz, A., & Barrera, E. V. (2020). Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug Release. Pharmaceutics, 12(12), 1208. https://doi.org/10.3390/pharmaceutics12121208
195. Skibba, M., Drelich, A., Poellmann, M., Hong, S., & Brasier, A. R. (2020). Nanoapproaches to Modifying Epigenetics of Epithelial Mesenchymal Transition for Treatment of Pulmonary Fibrosis. Frontiers in pharmacology, 11, 607689. https://doi.org/10.3389/fphar.2020.607689
196. Aliyandi, A., Zuhorn, I. S., & Salvati, A. (2020). Disentangling Biomolecular Corona Interactions With Cell Receptors and Implications for Targeting of Nanomedicines. Frontiers in bioengineering and biotechnology, 8, 599454. https://doi.org/10.3389/fbioe.2020.599454
197. Biancacci, I., Sun, Q., Möckel, D., Gremse, F., Rosenhain, S., Kiessling, F., Bartneck, M., Hu, Q., Thewissen, M., Storm, G., Hennink, W. E., Shi, Y., Rijcken, C., Lammers, T., & Sofias, A. M. (2020). Optical imaging of the whole-body to cellular biodistribution of clinical-stage PEG-b-pHPMA-based core-crosslinked polymeric micelles. Journal of controlled release : official journal of the Controlled Release Society, 328, 805–816. https://doi.org/10.1016/j.jconrel.2020.09.046
198. Jacob, E. M., Borah, A., Pillai, S. C., & Kumar, D. S. (2020). Inflammatory Bowel Disease: The Emergence of New Trends in Lifestyle and Nanomedicine as the Modern Tool for Pharmacotherapy. Nanomaterials (Basel, Switzerland), 10(12), 2460. https://doi.org/10.3390/nano10122460
199. Hu, H., & Steinmetz, N. F. (2020). Cisplatin Prodrug-Loaded Nanoparticles Based on Physalis Mottle Virus for Cancer Therapy. Molecular pharmaceutics, 17(12), 4629–4636. https://doi.org/10.1021/acs.molpharmaceut.0c00834
200. Zeb, A., Rana, I., Choi, H. I., Lee, C. H., Baek, S. W., Lim, C. W., Khan, N., Arif, S. T., Sahar, N. U., Alvi, A. M., Shah, F. A., Din, F. U., Bae, O. N., Park, J. S., & Kim, J. K. (2020). Potential and Applications of Nanocarriers for Efficient Delivery of Biopharmaceuticals. Pharmaceutics, 12(12), 1184. https://doi.org/10.3390/pharmaceutics12121184
201. Kakwere, H., Ingham, E. S., Tumbale, S. K., & Ferrara, K. W. (2020). Gemcitabine-retinoid prodrug loaded nanoparticles display in vitro antitumor efficacy towards drug-resilient human PANC-1 pancreatic cancer cells. Materials science & engineering. C, Materials for biological applications, 117, 111251. https://doi.org/10.1016/j.msec.2020.111251
202. Borden, M. A., Shakya, G., Upadhyay, A., & Song, K. H. (2020). Acoustic Nanodrops for Biomedical Applications. Current opinion in colloid & interface science, 50, 101383. https://doi.org/10.1016/j.cocis.2020.08.008
203. Zhou, Y., Que, K. T., Tang, H. M., Zhang, P., Fu, Q. M., & Liu, Z. J. (2020). Anti-CD206 antibody-conjugated Fe3O4-based PLGA nanoparticles selectively promote tumor-associated macrophages to polarize to the pro-inflammatory subtype. Oncology letters, 20(6), 298. https://doi.org/10.3892/ol.2020.12161
204. Barkovskaya, A., Buffone, A., Jr, Žídek, M., & Weaver, V. M. (2020). Proteoglycans as Mediators of Cancer Tissue Mechanics. Frontiers in cell and developmental biology, 8, 569377. https://doi.org/10.3389/fcell.2020.569377
205. Mediratta, K., El-Sahli, S., D'Costa, V., & Wang, L. (2020). Current Progresses and Challenges of Immunotherapy in Triple-Negative Breast Cancer. Cancers, 12(12), 3529. https://doi.org/10.3390/cancers12123529
206. Zhou, Y., Sun, X., Zhou, L., & Zhang, X. (2020). pH-Sensitive and Long-Circulation Nanoparticles for Near-Infrared Fluorescence Imaging-Monitored and Chemo-Photothermal Synergistic Treatment Against Gastric Cancer. Frontiers in pharmacology, 11, 610883. https://doi.org/10.3389/fphar.2020.610883
207. Jin, Y., Wang, Y., Liu, X., Zhou, J., Wang, X., Feng, H., & Liu, H. (2020). Synergistic Combination Chemotherapy of Lung Cancer: Cisplatin and Doxorubicin Conjugated Prodrug Loaded, Glutathione and pH Sensitive Nanocarriers. Drug design, development and therapy, 14, 5205–5215. https://doi.org/10.2147/DDDT.S260253
208. Wang, X., Qiu, Y., Wang, M., Zhang, C., Zhang, T., Zhou, H., Zhao, W., Zhao, W., Xia, G., & Shao, R. (2020). Endocytosis and Organelle Targeting of Nanomedicines in Cancer Therapy. International journal of nanomedicine, 15, 9447–9467. https://doi.org/10.2147/IJN.S274289
209. Yoo, J. D., Bae, S. M., Seo, J., Jeon, I. S., Vadevoo, S., Kim, S. Y., Kim, I. S., Lee, B., & Kim, S. (2020). Designed ferritin nanocages displaying trimeric TRAIL and tumor-targeting peptides confer superior anti-tumor efficacy. Scientific reports, 10(1), 19997. https://doi.org/10.1038/s41598-020-77095-x
210. Siamof, C. M., Goel, S., & Cai, W. (2020). Moving Beyond the Pillars of Cancer Treatment: Perspectives From Nanotechnology. Frontiers in chemistry, 8, 598100. https://doi.org/10.3389/fchem.2020.598100
211. Coclite, A., Coclite, G. M., & De Tommasi, D. (2020). Capsules Rheology in Carreau-Yasuda Fluids. Nanomaterials (Basel, Switzerland), 10(11), 2190. https://doi.org/10.3390/nano10112190
212. Alqahtani, M. S., Syed, R., & Alshehri, M. (2020). Size-Dependent Phagocytic Uptake and Immunogenicity of Gliadin Nanoparticles. Polymers, 12(11), 2576. https://doi.org/10.3390/polym12112576
213. Li, X., Lovell, J. F., Yoon, J., & Chen, X. (2020). Clinical development and potential of photothermal and photodynamic therapies for cancer. Nature reviews. Clinical oncology, 17(11), 657–674. https://doi.org/10.1038/s41571-020-0410-2
214. Rehman, F. U., Al-Waeel, M., Naz, S. S., & Shah, K. U. (2020). Anticancer therapeutics: a brief account on wide refinements. American journal of cancer research, 10(11), 3599–3621.
215. Zhu, Y., Yu, X., Thamphiwatana, S. D., Zheng, Y., & Pang, Z. (2020). Nanomedicines modulating tumor immunosuppressive cells to enhance cancer immunotherapy. Acta pharmaceutica Sinica. B, 10(11), 2054–2074. https://doi.org/10.1016/j.apsb.2020.08.010
216. Xie, M., Xu, Y., Huang, J., Li, Y., Wang, L., Yang, L., & Mao, H. (2020). Going even smaller: Engineering sub-5 nm nanoparticles for improved delivery, biocompatibility, and functionality. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 12(6), e1644. https://doi.org/10.1002/wnan.1644
217. Gaspar, R., Coelho, F., & Silva, B. (2020). Lipid-Nucleic Acid Complexes: Physicochemical Aspects and Prospects for Cancer Treatment. Molecules (Basel, Switzerland), 25(21), 5006. https://doi.org/10.3390/molecules25215006
218. Clement, S., Campbell, J. M., Deng, W., Guller, A., Nisar, S., Liu, G., Wilson, B. C., & Goldys, E. M. (2020). Mechanisms for Tuning Engineered Nanomaterials to Enhance Radiation Therapy of Cancer. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 7(24), 2003584. https://doi.org/10.1002/advs.202003584
219. Liang, Z., Li, J., & Zhu, B. (2020). Lung Cancer Combination Treatment: Evaluation of the Synergistic Effect of Cisplatin Prodrug, Vinorelbine and Retinoic Acid When Co-Encapsulated in a Multi-Layered Nano-Platform. Drug design, development and therapy, 14, 4519–4531. https://doi.org/10.2147/DDDT.S251749
220. Redolfi Riva, E., Sinibaldi, E., Grillone, A. F., Del Turco, S., Mondini, A., Li, T., Takeoka, S., & Mattoli, V. (2020). Enhanced In Vitro Magnetic Cell Targeting of Doxorubicin-Loaded Magnetic Liposomes for Localized Cancer Therapy. Nanomaterials (Basel, Switzerland), 10(11), 2104. https://doi.org/10.3390/nano10112104
221. Martin, B., Seguin, J., Annereau, M., Fleury, T., Lai-Kuen, R., Neri, G., Lam, A., Bally, M., Mignet, N., & Corvis, Y. (2020). Preparation of parenteral nanocrystal suspensions of etoposide from the excipient free dry state of the drug to enhance in vivo antitumoral properties. Scientific reports, 10(1), 18059. https://doi.org/10.1038/s41598-020-74809-z
222. Hassani, A., Azarian, M., Ibrahim, W. N., & Hussain, S. A. (2020). Preparation, characterization and therapeutic properties of gum arabic-stabilized gallic acid nanoparticles. Scientific reports, 10(1), 17808. https://doi.org/10.1038/s41598-020-71175-8
223. Jiang, B., Zhou, L., Lu, J., Wang, Y., Liu, C., You, L., & Guo, J. (2020). Stroma-Targeting Therapy in Pancreatic Cancer: One Coin With Two Sides?. Frontiers in oncology, 10, 576399. https://doi.org/10.3389/fonc.2020.576399
224. Wonder, E. A., Ewert, K. K., Liu, C., Steffes, V. M., Kwak, J., Qahar, V., Majzoub, R. N., Zhang, Z., Carragher, B., Potter, C. S., Li, Y., Qiao, W., & Safinya, C. R. (2020). Assembly of Building Blocks by Double-End-Anchored Polymers in the Dilute Regime Mediated by Hydrophobic Interactions at Controlled Distances. ACS applied materials & interfaces, 12(41), 45728–45743. https://doi.org/10.1021/acsami.0c10972
225. Eckmann, D. M., Bradley, R. P., Kandy, S. K., Patil, K., Janmey, P. A., & Radhakrishnan, R. (2020). Multiscale modeling of protein membrane interactions for nanoparticle targeting in drug delivery. Current opinion in structural biology, 64, 104–110. https://doi.org/10.1016/j.sbi.2020.06.023
226. Scherger, M., Bolli, E., Antunes, A., Arnouk, S., Stickdorn, J., Van Driessche, A., Schild, H., Grabbe, S., De Geest, B. G., Van Ginderachter, J. A., & Nuhn, L. (2020). Transient Multivalent Nanobody Targeting to CD206-Expressing Cells via PH-Degradable Nanogels. Cells, 9(10), 2222. https://doi.org/10.3390/cells9102222
227. Wang, S., Duan, Y., Zhang, Q., Komarla, A., Gong, H., Gao, W., & Zhang, L. (2020). Drug Targeting via Platelet Membrane-Coated Nanoparticles. Small structures, 1(1), 2000018. https://doi.org/10.1002/sstr.202000018
228. Hattab, D., & Bakhtiar, A. (2020). Bioengineered siRNA-Based Nanoplatforms Targeting Molecular Signaling Pathways for the Treatment of Triple Negative Breast Cancer: Preclinical and Clinical Advancements. Pharmaceutics, 12(10), 929. https://doi.org/10.3390/pharmaceutics12100929
229. Wei, Q. Y., Xu, Y. M., & Lau, A. (2020). Recent Progress of Nanocarrier-Based Therapy for Solid Malignancies. Cancers, 12(10), 2783. https://doi.org/10.3390/cancers12102783
230. Wu, C., Wu, K. J., Liu, J. B., Wang, W., Leung, C. H., & Ma, D. L. (2020). Structure-guided discovery of a luminescent theranostic toolkit for living cancer cells and the imaging behavior effect. Chemical science, 11(42), 11404–11412. https://doi.org/10.1039/d0sc04576d
231. Mohanty, A., Uthaman, S., & Park, I. K. (2020). Utilization of Polymer-Lipid Hybrid Nanoparticles for Targeted Anti-Cancer Therapy. Molecules (Basel, Switzerland), 25(19), 4377. https://doi.org/10.3390/molecules25194377
232. González-Larraza, P. G., López-Goerne, T. M., Padilla-Godínez, F. J., González-López, M. A., Hamdan-Partida, A., & Gómez, E. (2020). IC50 Evaluation of Platinum Nanocatalysts for Cancer Treatment in Fibroblast, HeLa, and DU-145 Cell Lines. ACS omega, 5(39), 25381–25389. https://doi.org/10.1021/acsomega.0c03759
233. Gurunathan, S., Jeyaraj, M., Kang, M. H., & Kim, J. H. (2020). Anticancer Properties of Platinum Nanoparticles and Retinoic Acid: Combination Therapy for the Treatment of Human Neuroblastoma Cancer. International journal of molecular sciences, 21(18), 6792. https://doi.org/10.3390/ijms21186792
234. Yu, W. J., Huang, D. X., Liu, S., Sha, Y. L., Gao, F. H., & Liu, H. (2020). Polymeric Nanoscale Drug Carriers Mediate the Delivery of Methotrexate for Developing Therapeutic Interventions Against Cancer and Rheumatoid Arthritis. Frontiers in oncology, 10, 1734. https://doi.org/10.3389/fonc.2020.01734
235. Xia, J., Xue, Y., Lei, B., Xu, L., Sun, M., Li, N., Zhao, H., Wang, M., Luo, M., Zhang, C., Huang, B., Du, Y., & Yan, C. H. (2020). Multimodal channel cancer chemotherapy by 2D functional gadolinium metal-organic framework. National science review, 8(7), nwaa221. https://doi.org/10.1093/nsr/nwaa221
236. Fuchs, N., Meta, M., Schuppan, D., Nuhn, L., & Schirmeister, T. (2020). Novel Opportunities for Cathepsin S Inhibitors in Cancer Immunotherapy by Nanocarrier-Mediated Delivery. Cells, 9(9), 2021. https://doi.org/10.3390/cells9092021
237. Day, R. A., Estabrook, D. A., Wu, C., Chapman, J. O., Togle, A. J., & Sletten, E. M. (2020). Systematic Study of Perfluorocarbon Nanoemulsions Stabilized by Polymer Amphiphiles. ACS applied materials & interfaces, 12(35), 38887–38898. https://doi.org/10.1021/acsami.0c07206
238. Selvaraja, V. K., & Gudipudi, D. K. (2020). Fundamentals to clinical application of nanoparticles in cancer immunotherapy and radiotherapy. Ecancermedicalscience, 14, 1095. https://doi.org/10.3332/ecancer.2020.1095
239. Davis, H. W., Vallabhapurapu, S. D., Chu, Z., Wyder, M. A., Greis, K. D., Fannin, V., Sun, Y., Desai, P. B., Pak, K. Y., Gray, B. D., & Qi, X. (2020). Biotherapy of Brain Tumors with Phosphatidylserine-Targeted Radioiodinated SapC-DOPS Nanovesicles. Cells, 9(9), 1960. https://doi.org/10.3390/cells9091960
240. Liu, Y., van Steenbergen, M. J., Zhong, Z., Oliveira, S., Hennink, W. E., & van Nostrum, C. F. (2020). Dithiolane-Crosslinked Poly(ε-caprolactone)-Based Micelles: Impact of Monomer Sequence, Nature of Monomer, and Reducing Agent on the Dynamic Crosslinking Properties. Macromolecules, 53(16), 7009–7024. https://doi.org/10.1021/acs.macromol.0c01031
241. Liu, M., Tu, J., Feng, Y., Zhang, J., & Wu, J. (2020). Synergistic co-delivery of diacid metabolite of norcantharidin and ABT-737 based on folate-modified lipid bilayer-coated mesoporous silica nanoparticle against hepatic carcinoma. Journal of nanobiotechnology, 18(1), 114. https://doi.org/10.1186/s12951-020-00677-4
242. Wong, K. H., Lu, A., Chen, X., & Yang, Z. (2020). Natural Ingredient-Based Polymeric Nanoparticles for Cancer Treatment. Molecules (Basel, Switzerland), 25(16), 3620. https://doi.org/10.3390/molecules25163620
243. Demirbağ Karaali, M., & Aydın Karataş, E. (2020). Investigation of the potential anticancer effects of napelline and talatisamine dirterpenes on experimental brain tumor models. Cytotechnology, 72(4), 569–578. https://doi.org/10.1007/s10616-020-00405-8
244. Hajiahmadi, Z., Shirzadian-Khorramabad, R., Kazemzad, M., Sohani, M. M., & Khajehali, J. (2020). A novel, simple, and stable mesoporous silica nanoparticle-based gene transformation approach in Solanum lycopersicum. 3 Biotech, 10(8), 370. https://doi.org/10.1007/s13205-020-02359-2
245. Ferreira, D., Fontinha, D., Martins, C., Pires, D., Fernandes, A. R., & Baptista, P. V. (2020). Gold Nanoparticles for Vectorization of Nucleic Acids for Cancer Therapeutics. Molecules (Basel, Switzerland), 25(15), 3489. https://doi.org/10.3390/molecules25153489
246. Michael, P., Lam, Y. T., Filipe, E. C., Tan, R. P., Chan, A., Lee, B., Feng, N., Hung, J., Cox, T. R., Santos, M., & Wise, S. G. (2020). Plasma polymerized nanoparticles effectively deliver dual siRNA and drug therapy in vivo. Scientific reports, 10(1), 12836. https://doi.org/10.1038/s41598-020-69591-x
247. Sarkar, N., Morton, H., & Bose, S. (2020). Effects of vitamin C on osteoblast proliferation and osteosarcoma inhibition using plasma coated hydroxyapatite on titanium implants. Surface & coatings technology, 394, 125793. https://doi.org/10.1016/j.surfcoat.2020.125793
248. Kargozar, S., , Baino, F., , Hamzehlou, S., , Hamblin, M. R., , & Mozafari, M., (2020). Nanotechnology for angiogenesis: opportunities and challenges. Chemical Society reviews, 49(14), 5008–5057. https://doi.org/10.1039/c8cs01021h
249. Lu, L., Zhang, C., Zou, B., & Wang, Y. (2020). Hollow Prussian Blue Nanospheres for Photothermal/Chemo-Synergistic Therapy. International journal of nanomedicine, 15, 5165–5177. https://doi.org/10.2147/IJN.S252505
250. Wang, Z., Chen, J., Little, N., & Lu, J. (2020). Self-assembling prodrug nanotherapeutics for synergistic tumor targeted drug delivery. Acta biomaterialia, 111, 20–28. https://doi.org/10.1016/j.actbio.2020.05.026
251. Shao, W., Yang, C., Li, F., Wu, J., Wang, N., Ding, Q., Gao, J., & Ling, D. (2020). Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT. Nano-micro letters, 12(1), 147. https://doi.org/10.1007/s40820-020-00474-6
252. Gao, J., Wang, W. Q., Pei, Q., Lord, M. S., & Yu, H. J. (2020). Engineering nanomedicines through boosting immunogenic cell death for improved cancer immunotherapy. Acta pharmacologica Sinica, 41(7), 986–994. https://doi.org/10.1038/s41401-020-0400-z
253. Sun, Q., Bai, X., Sofias, A. M., van der Meel, R., Ruiz-Hernandez, E., Storm, G., Hennink, W. E., De Geest, B., Kiessling, F., Yu, H. J., Lammers, T., & Shi, Y. (2020). Cancer nanomedicine meets immunotherapy: opportunities and challenges. Acta pharmacologica Sinica, 41(7), 954–958. https://doi.org/10.1038/s41401-020-0448-9
254. Mirsafaei, R., & Varshosaz, J. (2020). Polyacrylamide-punicic acid conjugate-based micelles for flutamide delivery in PC3 cells of prostate cancer: synthesis, characterisation and cytotoxicity studies. IET nanobiotechnology, 14(5), 417–422. https://doi.org/10.1049/iet-nbt.2020.0014
255. Lai, Y. H., Chiang, C. S., Hsu, C. H., Cheng, H. W., & Chen, S. Y. (2020). Development and Characterization of a Fucoidan-Based Drug Delivery System by Using Hydrophilic Anticancer Polysaccharides to Simultaneously Deliver Hydrophobic Anticancer Drugs. Biomolecules, 10(7), 970. https://doi.org/10.3390/biom10070970
256. Manivannan, S., & Ponnuchamy, K. (2020). Quantum dots as a promising agent to combat COVID-19. Applied organometallic chemistry, e5887. Advance online publication. https://doi.org/10.1002/aoc.5887
257. Rajora, A. K., Ravishankar, D., Zhang, H., & Rosenholm, J. M. (2020). Recent Advances and Impact of Chemotherapeutic and Antiangiogenic Nanoformulations for Combination Cancer Therapy. Pharmaceutics, 12(6), 592. https://doi.org/10.3390/pharmaceutics12060592
258. Singh, N., Millot, N., Maurizi, L., Lizard, G., & Kumar, R. (2020). Taurine-Conjugated Mussel-Inspired Iron Oxide Nanoparticles with an Elongated Shape for Effective Delivery of Doxorubicin into the Tumor Cells. ACS omega, 5(26), 16165–16175. https://doi.org/10.1021/acsomega.0c01747
259. Peng, C., Huang, Y., & Zheng, J. (2020). Renal clearable nanocarriers: Overcoming the physiological barriers for precise drug delivery and clearance. Journal of controlled release : official journal of the Controlled Release Society, 322, 64–80. https://doi.org/10.1016/j.jconrel.2020.03.020
260. Montaseri, H., Kruger, C. A., & Abrahamse, H. (2020). Review: Organic nanoparticle based active targeting for photodynamic therapy treatment of breast cancer cells. Oncotarget, 11(22), 2120–2136. https://doi.org/10.18632/oncotarget.27596
261. Zaki, A. G., El-Sayed, E. R., Abd Elkodous, M., & El-Sayyad, G. S. (2020). Microbial acetylcholinesterase inhibitors for Alzheimer's therapy: recent trends on extraction, detection, irradiation-assisted production improvement and nano-structured drug delivery. Applied microbiology and biotechnology, 104(11), 4717–4735. https://doi.org/10.1007/s00253-020-10560-9
262. Lemmerman, L. R., Das, D., Higuita-Castro, N., Mirmira, R. G., & Gallego-Perez, D. (2020). Nanomedicine-Based Strategies for Diabetes: Diagnostics, Monitoring, and Treatment. Trends in endocrinology and metabolism: TEM, 31(6), 448–458. https://doi.org/10.1016/j.tem.2020.02.001
263. Kazakov, A. G., Garashchenko, B. L., Ivanova, M. K., Vinokurov, S. E., & Myasoedov, B. F. (2020). Carbon Nanomaterials for Sorption of 68Ga for Potential Using in Positron Emission Tomography. Nanomaterials (Basel, Switzerland), 10(6), 1090. https://doi.org/10.3390/nano10061090
264. Guo, Q., & Jiang, C. (2020). Delivery strategies for macromolecular drugs in cancer therapy. Acta pharmaceutica Sinica. B, 10(6), 979–986. https://doi.org/10.1016/j.apsb.2020.01.009
265. Prasad, C., Bhatia, E., & Banerjee, R. (2020). Curcumin Encapsulated Lecithin Nanoemulsions: An Oral Platform for Ultrasound Mediated Spatiotemporal Delivery of Curcumin to the Tumor. Scientific reports, 10(1), 8587. https://doi.org/10.1038/s41598-020-65468-1
266. Tatiparti, K., Rauf, M. A., Sau, S., & Iyer, A. K. (2020). Carbonic Anhydrase-IX Guided Albumin Nanoparticles for Hypoxia-mediated Triple-Negative Breast Cancer Cell Killing and Imaging of Patient-derived Tumor. Molecules (Basel, Switzerland), 25(10), 2362. https://doi.org/10.3390/molecules25102362
267. Martinelli, C., Battaglini, M., Pucci, C., Gioi, S., Caracci, C., Macaluso, G., Doccini, S., Santorelli, F. M., & Ciofani, G. (2020). Development of Nanostructured Lipid Carriers for the Delivery of Idebenone in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. ACS omega, 5(21), 12451–12466. https://doi.org/10.1021/acsomega.0c01282
268. Su, T., Yang, B., Gao, T., Liu, T., & Li, J. (2020). Polymer nanoparticle-assisted chemotherapy of pancreatic cancer. Therapeutic advances in medical oncology, 12, 1758835920915978. https://doi.org/10.1177/1758835920915978
269. Alhajj, N., Zakaria, Z., Naharudin, I., Ahsan, F., Li, W., & Wong, T. W. (2020). Critical physicochemical attributes of chitosan nanoparticles admixed lactose-PEG 3000 microparticles in pulmonary inhalation. Asian journal of pharmaceutical sciences, 15(3), 374–384. https://doi.org/10.1016/j.ajps.2019.02.001
270. Zhang, X., Liu, Y., Gopalakrishnan, S., Castellanos-Garcia, L., Li, G., Malassiné, M., Uddin, I., Huang, R., Luther, D. C., Vachet, R. W., & Rotello, V. M. (2020). Intracellular Activation of Bioorthogonal Nanozymes through Endosomal Proteolysis of the Protein Corona. ACS nano, 14(4), 4767–4773. https://doi.org/10.1021/acsnano.0c00629
271. Zheng, D., Yu, P., Wei, Z., Zhong, C., Wu, M., & Liu, X. (2020). RBC Membrane Camouflaged Semiconducting Polymer Nanoparticles for Near-Infrared Photoacoustic Imaging and Photothermal Therapy. Nano-micro letters, 12(1), 94. https://doi.org/10.1007/s40820-020-00429-x
272. Layek, B., Shetty, M., Nethi, S. K., Sehgal, D., Starr, T. K., & Prabha, S. (2020). Mesenchymal Stem Cells As Guideposts for Nanoparticle-Mediated Targeted Drug Delivery in Ovarian Cancer. Cancers, 12(4), 965. https://doi.org/10.3390/cancers12040965
273. Sanna, V., & Sechi, M. (2020). Therapeutic Potential of Targeted Nanoparticles and Perspective on Nanotherapies. ACS medicinal chemistry letters, 11(6), 1069–1073. https://doi.org/10.1021/acsmedchemlett.0c00075
274. Song, W., Das, M., & Chen, X. (2020). Nanotherapeutics for Immuno-Oncology: A Crossroad for New Paradigms. Trends in cancer, 6(4), 288–298. https://doi.org/10.1016/j.trecan.2020.01.011
275. Cheng, Y. H., He, C., Riviere, J. E., Monteiro-Riviere, N. A., & Lin, Z. (2020). Meta-Analysis of Nanoparticle Delivery to Tumors Using a Physiologically Based Pharmacokinetic Modeling and Simulation Approach. ACS nano, 14(3), 3075–3095. https://doi.org/10.1021/acsnano.9b08142
276. Haider, M., Abdin, S. M., Kamal, L., & Orive, G. (2020). Nanostructured Lipid Carriers for Delivery of Chemotherapeutics: A Review. Pharmaceutics, 12(3), 288. https://doi.org/10.3390/pharmaceutics12030288
277. Levit, S. L., Yang, H., & Tang, C. (2020). Rapid Self-Assembly of Polymer Nanoparticles for Synergistic Codelivery of Paclitaxel and Lapatinib via Flash NanoPrecipitation. Nanomaterials (Basel, Switzerland), 10(3), 561. https://doi.org/10.3390/nano10030561
278. Agabeigi, R., Rasta, S. H., Rahmati-Yamchi, M., Salehi, R., & Alizadeh, E. (2020). Novel Chemo-Photothermal Therapy in Breast Cancer Using Methotrexate-Loaded Folic Acid Conjugated Au@SiO2 Nanoparticles. Nanoscale research letters, 15(1), 62. https://doi.org/10.1186/s11671-020-3295-1
279. Wang, J., Wu, X., Shen, P., Wang, J., Shen, Y., Shen, Y., Webster, T. J., & Deng, J. (2020). Applications of Inorganic Nanomaterials in Photothermal Therapy Based on Combinational Cancer Treatment. International journal of nanomedicine, 15, 1903–1914. https://doi.org/10.2147/IJN.S239751
280. Guo, F., Fu, Q., Zhou, K., Jin, C., Wu, W., Ji, X., Yan, Q., Yang, Q., Wu, D., Li, A., & Yang, G. (2020). Matrix metalloprotein-triggered, cell penetrating peptide-modified star-shaped nanoparticles for tumor targeting and cancer therapy. Journal of nanobiotechnology, 18(1), 48. https://doi.org/10.1186/s12951-020-00595-5
281. Mahdavi, M., Fattahi, A., Tajkhorshid, E., & Nouranian, S. (2020). Molecular Insights into the Loading and Dynamics of Doxorubicin on PEGylated Graphene Oxide Nanocarriers. ACS applied bio materials, 3(3), 1354–1363. https://doi.org/10.1021/acsabm.9b00956
282. Mi P. (2020). Stimuli-responsive nanocarriers for drug delivery, tumor imaging, therapy and theranostics. Theranostics, 10(10), 4557–4588. https://doi.org/10.7150/thno.38069
283. Xiong, D., Wen, L., Peng, S., Xu, J., & Zhang, L. (2020). Reversible Cross-Linked Mixed Micelles for pH Triggered Swelling and Redox Triggered Degradation for Enhanced and Controlled Drug Release. Pharmaceutics, 12(3), 258. https://doi.org/10.3390/pharmaceutics12030258
284. Ren, X., Zhang, P., & Chen, Z. (2020). Dialysis Preparation of Smart Redox and Acidity Dual Responsive Tea Polyphenol Functionalized Calcium Phosphate Nanospheres as Anticancer Drug Carriers. Molecules (Basel, Switzerland), 25(5), 1221. https://doi.org/10.3390/molecules25051221
285. Weng, Y., Huang, Q., Li, C., Yang, Y., Wang, X., Yu, J., Huang, Y., & Liang, X. J. (2020). Improved Nucleic Acid Therapy with Advanced Nanoscale Biotechnology. Molecular therapy. Nucleic acids, 19, 581–601. https://doi.org/10.1016/j.omtn.2019.12.004
286. Ali, I., Alsehli, M., Scotti, L., Tullius Scotti, M., Tsai, S. T., Yu, R. S., Hsieh, M. F., & Chen, J. C. (2020). Progress in Polymeric Nano-Medicines for Theranostic Cancer Treatment. Polymers, 12(3), 598. https://doi.org/10.3390/polym12030598
287. Su, H., Wang, F., Ran, W., Zhang, W., Dai, W., Wang, H., Anderson, C. F., Wang, Z., Zheng, C., Zhang, P., Li, Y., & Cui, H. (2020). The role of critical micellization concentration in efficacy and toxicity of supramolecular polymers. Proceedings of the National Academy of Sciences of the United States of America, 117(9), 4518–4526. https://doi.org/10.1073/pnas.1913655117
288. Palanikumar, L., Al-Hosani, S., Kalmouni, M., Nguyen, V. P., Ali, L., Pasricha, R., Barrera, F. N., & Magzoub, M. (2020). pH-responsive high stability polymeric nanoparticles for targeted delivery of anticancer therapeutics. Communications biology, 3(1), 95. https://doi.org/10.1038/s42003-020-0817-4
289. Tolliver, L. M., Holl, N. J., Hou, F., Lee, H. J., Cambre, M. H., & Huang, Y. W. (2020). Differential Cytotoxicity Induced by Transition Metal Oxide Nanoparticles is a Function of Cell Killing and Suppression of Cell Proliferation. International journal of molecular sciences, 21(5), 1731. https://doi.org/10.3390/ijms21051731
290. Ruman, U., Fakurazi, S., Masarudin, M. J., & Hussein, M. Z. (2020). Nanocarrier-Based Therapeutics and Theranostics Drug Delivery Systems for Next Generation of Liver Cancer Nanodrug Modalities. International journal of nanomedicine, 15, 1437–1456. https://doi.org/10.2147/IJN.S236927
291. Ashihara, K., Terai, Y., Tanaka, T., Tanaka, Y., Fujiwara, S., Maeda, K., Tunetoh, S., Sasaki, H., Hayashi, M., & Ohmichi, M. (2020). Pharmacokinetic evaluation and antitumor potency of liposomal nanoparticle encapsulated cisplatin targeted to CD24-positive cells in ovarian cancer. Oncology letters, 19(3), 1872–1880. https://doi.org/10.3892/ol.2020.11279
292. Xu, H., Ma, B., Jiang, J., Xiao, S., Peng, R., Zhuang, W., Li, G., & Wang, Y. (2020). Integrated prodrug micelles with two-photon bioimaging and pH-triggered drug delivery for cancer theranostics. Regenerative biomaterials, 7(2), 171–180. https://doi.org/10.1093/rb/rbz035
293. Fang, J., Hsueh, Y. Y., Soto, J., Sun, W., Wang, J., Gu, Z., Khademhosseini, A., & Li, S. (2020). Engineering Biomaterials with Micro/Nanotechnologies for Cell Reprogramming. ACS nano, 14(2), 1296–1318. https://doi.org/10.1021/acsnano.9b04837
294. Liu, Z., Cao, T., Xue, Y., Li, M., Wu, M., Engle, J. W., He, Q., Cai, W., Lan, M., & Zhang, W. (2020). Self-Amplified Photodynamic Therapy through the 1 O2 -Mediated Internalization of Photosensitizers from a Ppa-Bearing Block Copolymer. Angewandte Chemie (International ed. in English), 59(9), 3711–3717. https://doi.org/10.1002/anie.201914434
295. Vigata, M., Meinert, C., Pahoff, S., Bock, N., & Hutmacher, D. W. (2020). Gelatin Methacryloyl Hydrogels Control the Localized Delivery of Albumin-Bound Paclitaxel. Polymers, 12(2), 501. https://doi.org/10.3390/polym12020501
296. Baboci, L., Capolla, S., Di Cintio, F., Colombo, F., Mauro, P., Dal Bo, M., Argenziano, M., Cavalli, R., Toffoli, G., & Macor, P. (2020). The Dual Role of the Liver in Nanomedicine as an Actor in the Elimination of Nanostructures or a Therapeutic Target. Journal of oncology, 2020, 4638192. https://doi.org/10.1155/2020/4638192
297. Amerigos Daddy J C, K., Chen, M., Raza, F., Xiao, Y., Su, Z., & Ping, Q. (2020). Co-Encapsulation of Mitoxantrone and β-Elemene in Solid Lipid Nanoparticles to Overcome Multidrug Resistance in Leukemia. Pharmaceutics, 12(2), 191. https://doi.org/10.3390/pharmaceutics12020191
298. Nuñez-Rivera, A., Fournier, P., Arellano, D. L., Rodriguez-Hernandez, A. G., Vazquez-Duhalt, R., & Cadena-Nava, R. D. (2020). Brome mosaic virus-like particles as siRNA nanocarriers for biomedical purposes. Beilstein journal of nanotechnology, 11, 372–382. https://doi.org/10.3762/bjnano.11.28
299. Li, J., Jia, Y., Zhang, P., Yang, H., Cong, X., An, L., & Xiao, C. (2020). Celastrol Self-Stabilized Nanoparticles for Effective Treatment of Melanoma. International journal of nanomedicine, 15, 1205–1214. https://doi.org/10.2147/IJN.S232603
300. Ferreira, M., Rizzuti, I. F., Palange, A. L., Barbato, M. G., Di Francesco, V., Di Francesco, M., & Decuzzi, P. (2020). Optimizing the Pharmacological Properties of Discoidal Polymeric Nanoconstructs Against Triple-Negative Breast Cancer Cells. Frontiers in bioengineering and biotechnology, 8, 5. https://doi.org/10.3389/fbioe.2020.00005
301. Yang, M., Yang, W., Chen, L., Ding, M., Li, C., & Shi, D. (2020). A Novel Synthesis of Fe3O4@SiO2@Au@Porous SiO2 Structure for NIR Irradiation-Induced DOX Release and Cancer Treatment. Dose-response : a publication of International Hormesis Society, 18(1), 1559325820906662. https://doi.org/10.1177/1559325820906662
302. Francia, V., Montizaan, D., & Salvati, A. (2020). Interactions at the cell membrane and pathways of internalization of nano-sized materials for nanomedicine. Beilstein journal of nanotechnology, 11, 338–353. https://doi.org/10.3762/bjnano.11.25
303. Chibh, S., Kour, A., Yadav, N., Kumar, P., Yadav, P., Chauhan, V. S., & Panda, J. J. (2020). Redox-Responsive Dipeptide Nanostructures toward Targeted Cancer Therapy. ACS omega, 5(7), 3365–3375. https://doi.org/10.1021/acsomega.9b03547
304. Wirthl, B., Kremheller, J., Schrefler, B. A., & Wall, W. A. (2020). Extension of a multiphase tumour growth model to study nanoparticle delivery to solid tumours. PloS one, 15(2), e0228443. https://doi.org/10.1371/journal.pone.0228443
305. Hashemzadeh, H., Javadi, H., & Darvishi, M. H. (2020). Study of Structural stability and formation mechanisms in DSPC and DPSM liposomes: A coarse-grained molecular dynamics simulation. Scientific reports, 10(1), 1837. https://doi.org/10.1038/s41598-020-58730-z
306. Li, S., Liu, J., Sun, M., Wang, J., Wang, C., & Sun, Y. (2020). Cell Membrane-Camouflaged Nanocarriers for Cancer Diagnostic and Therapeutic. Frontiers in pharmacology, 11, 24. https://doi.org/10.3389/fphar.2020.00024
307. Jovčevska, I., & Muyldermans, S. (2020). The Therapeutic Potential of Nanobodies. BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 34(1), 11–26. https://doi.org/10.1007/s40259-019-00392-z
308. Bang, Y. J., Li, C. P., Lee, K. H., Chiu, C. F., Park, J. O., Shan, Y. S., Kim, J. S., Chen, J. S., Shim, H. J., Rau, K. M., Choi, H. J., Oh, D. Y., Belanger, B., & Chen, L. T. (2020). Liposomal irinotecan in metastatic pancreatic adenocarcinoma in Asian patients: Subgroup analysis of the NAPOLI-1 study. Cancer science, 111(2), 513–527. https://doi.org/10.1111/cas.14264
309. Kang, H., Stiles, W. R., Baek, Y., Nomura, S., Bao, K., Hu, S., Park, G. K., Jo, M. J., I, H., Coll, J. L., Rubin, B. P., & Choi, H. S. (2020). Renal Clearable Theranostic Nanoplatforms for Gastrointestinal Stromal Tumors. Advanced materials (Deerfield Beach, Fla.), 32(6), e1905899. https://doi.org/10.1002/adma.201905899
310. Rabiee, N., Yaraki, M. T., Garakani, S. M., Garakani, S. M., Ahmadi, S., Lajevardi, A., Bagherzadeh, M., Rabiee, M., Tayebi, L., Tahriri, M., & Hamblin, M. R. (2020). Recent advances in porphyrin-based nanocomposites for effective targeted imaging and therapy. Biomaterials, 232, 119707. https://doi.org/10.1016/j.biomaterials.2019.119707
311. Al-Refaei, M. A., Makki, R. M., & Ali, H. M. (2020). Structure prediction of transferrin receptor protein 1 (TfR1) by homology modelling, docking, and molecular dynamics simulation studies. Heliyon, 6(1), e03221. https://doi.org/10.1016/j.heliyon.2020.e03221
312. Peng, R., Ji, H., Jin, L., Lin, S., Huang, Y., Xu, K., Yang, Q., Sun, D., & Wu, W. (2020). Macrophage-Based Therapies for Atherosclerosis Management. Journal of immunology research, 2020, 8131754. https://doi.org/10.1155/2020/8131754
313. Bhattacharyya, S., & Ghosh, S. S. (2020). Transmembrane TNFα-Expressed Macrophage Membrane-Coated Chitosan Nanoparticles as Cancer Therapeutics. ACS omega, 5(3), 1572–1580. https://doi.org/10.1021/acsomega.9b03531
314. Mahmoud, B. S., AlAmri, A. H., & McConville, C. (2020). Polymeric Nanoparticles for the Treatment of Malignant Gliomas. Cancers, 12(1), 175. https://doi.org/10.3390/cancers12010175
315. Chauhan, N., Kruse, A., Newby, H., Jaggi, M., Yallapu, M. M., & Chauhan, S. C. (2020). Pluronic Polymer-Based Ormeloxifene Nanoformulations Induce Superior Anticancer Effects in Pancreatic Cancer Cells. ACS omega, 5(2), 1147–1156. https://doi.org/10.1021/acsomega.9b03382
316. Jia, W., Burns, J. M., Villantay, B., Tang, J. C., Vankayala, R., Lertsakdadet, B., Choi, B., Nelson, J. S., & Anvari, B. (2020). Intravital Vascular Phototheranostics and Real-Time Circulation Dynamics of Micro- and Nanosized Erythrocyte-Derived Carriers. ACS applied materials & interfaces, 12(1), 275–287. https://doi.org/10.1021/acsami.9b18624
317. Liang, B. J., Pigula, M., Baglo, Y., Najafali, D., Hasan, T., & Huang, H. C. (2020). Breaking the selectivity-uptake trade-off of photoimmunoconjugates with nanoliposomal irinotecan for synergistic multi-tier cancer targeting. Journal of nanobiotechnology, 18(1), 1. https://doi.org/10.1186/s12951-019-0560-5
318. Lakkadwala, S., Dos Santos Rodrigues, B., Sun, C., & Singh, J. (2020). Biodistribution of TAT or QLPVM coupled to receptor targeted liposomes for delivery of anticancer therapeutics to brain in vitro and in vivo. Nanomedicine : nanotechnology, biology, and medicine, 23, 102112. https://doi.org/10.1016/j.nano.2019.102112
319. Dasgupta, A., Biancacci, I., Kiessling, F., & Lammers, T. (2020). Imaging-assisted anticancer nanotherapy. Theranostics, 10(3), 956–967. https://doi.org/10.7150/thno.38288
320. Zhao, M., van Straten, D., Broekman, M., Préat, V., & Schiffelers, R. M. (2020). Nanocarrier-based drug combination therapy for glioblastoma. Theranostics, 10(3), 1355–1372. https://doi.org/10.7150/thno.38147
321. Shi, J., Granger, B., Xu, K., & Yang, Y. (2020). Quantitative X-ray fluorescence imaging of gold nanoparticles using joint L1 and total variation regularized reconstruction. Quantitative imaging in medicine and surgery, 10(1), 184–196. https://doi.org/10.21037/qims.2019.10.15
322. Wilhelm, J., Wang, Z., Sumer, B. D., & Gao, J. (2020). Exploiting nanoscale cooperativity for precision medicine. Advanced drug delivery reviews, 158, 63–72. https://doi.org/10.1016/j.addr.2020.08.012
323. Yang, W., Veroniaina, H., Qi, X., Chen, P., Li, F., & Ke, P. C. (2020). Soft and Condensed Nanoparticles and Nanoformulations for Cancer Drug Delivery and Repurpose. Advanced therapeutics, 3(1), 1900102. https://doi.org/10.1002/adtp.201900102
324. Forte, E., Fiorenza, D., Torino, E., Costagliola di Polidoro, A., Cavaliere, C., Netti, P. A., Salvatore, M., & Aiello, M. (2019). Radiolabeled PET/MRI Nanoparticles for Tumor Imaging. Journal of clinical medicine, 9(1), 89. https://doi.org/10.3390/jcm9010089
325. Helal-Neto, E., Barros, A., Saldanha-Gama, R., Brandão-Costa, R., Alencar, L., Santos, C., Martínez-Máñez, R., Ricci-Junior, E., Alexis, F., Morandi, V., Barja-Fidalgo, C., & Santos-Oliveira, R. (2019). Molecular and Cellular Risk Assessment of Healthy Human Cells and Cancer Human Cells Exposed to Nanoparticles. International journal of molecular sciences, 21(1), 230. https://doi.org/10.3390/ijms21010230
326. Mazzotta, E., De Benedittis, S., Qualtieri, A., & Muzzalupo, R. (2019). Actively Targeted and Redox Responsive Delivery of Anticancer Drug by Chitosan Nanoparticles. Pharmaceutics, 12(1), 26. https://doi.org/10.3390/pharmaceutics12010026
327. Youssef, F. S., El-Banna, H. A., Elzorba, H. Y., & Galal, A. M. (2019). Application of some nanoparticles in the field of veterinary medicine. International journal of veterinary science and medicine, 7(1), 78–93. https://doi.org/10.1080/23144599.2019.1691379
328. Lumen, D., Näkki, S., Imlimthan, S., Lambidis, E., Sarparanta, M., Xu, W., Lehto, V. P., & Airaksinen, A. J. (2019). Site-Specific 111In-Radiolabeling of Dual-PEGylated Porous Silicon Nanoparticles and Their In Vivo Evaluation in Murine 4T1 Breast Cancer Model. Pharmaceutics, 11(12), 686. https://doi.org/10.3390/pharmaceutics11120686
329. Saleem, K., Khursheed, Z., Hano, C., Anjum, I., & Anjum, S. (2019). Applications of Nanomaterials in Leishmaniasis: A Focus on Recent Advances and Challenges. Nanomaterials (Basel, Switzerland), 9(12), 1749. https://doi.org/10.3390/nano9121749
330. Morelli, L., Gimondi, S., Sevieri, M., Salvioni, L., Guizzetti, M., Colzani, B., Palugan, L., Foppoli, A., Talamini, L., Morosi, L., Zucchetti, M., Violatto, M. B., Russo, L., Salmona, M., Prosperi, D., Colombo, M., & Bigini, P. (2019). Monitoring the Fate of Orally Administered PLGA Nanoformulation for Local Delivery of Therapeutic Drugs. Pharmaceutics, 11(12), 658. https://doi.org/10.3390/pharmaceutics11120658
331. Cristallini, C., Barbani, N., Bianchi, S., Maltinti, S., Baldassare, A., Ishak, R., Onor, M., Ambrosio, L., Castelvetro, V., & Cascone, M. G. (2019). Assessing two-way interactions between cells and inorganic nanoparticles. Journal of materials science. Materials in medicine, 31(1), 1. https://doi.org/10.1007/s10856-019-6328-5
332. Chen, Q., Bao, Y., Burner, D., Kaushal, S., Zhang, Y., Mendoza, T., Bouvet, M., Ozkan, C., Minev, B., & Ma, W. (2019). Tumor growth inhibition by mSTEAP peptide nanovaccine inducing augmented CD8+ T cell immune responses. Drug delivery and translational research, 9(6), 1095–1105. https://doi.org/10.1007/s13346-019-00652-z
333. Kita, Y., Hamada, A., Saito, R., Teramoto, Y., Tanaka, R., Takano, K., Nakayama, K., Murakami, K., Matsumoto, K., Akamatsu, S., Yamasaki, T., Inoue, T., Tabata, Y., Okuno, Y., Ogawa, O., & Kobayashi, T. (2019). Systematic chemical screening identifies disulfiram as a repurposed drug that enhances sensitivity to cisplatin in bladder cancer: a summary of preclinical studies. British journal of cancer, 121(12), 1027–1038. https://doi.org/10.1038/s41416-019-0609-0
334. Li, Y., Zhai, Y., Liu, W., Zhang, K., Liu, J., Shi, J., & Zhang, Z. (2019). Ultrasmall nanostructured drug based pH-sensitive liposome for effective treatment of drug-resistant tumor. Journal of nanobiotechnology, 17(1), 117. https://doi.org/10.1186/s12951-019-0550-7
335. Lin, F., Jia, H. R., & Wu, F. G. (2019). Glycol Chitosan: A Water-Soluble Polymer for Cell Imaging and Drug Delivery. Molecules (Basel, Switzerland), 24(23), 4371. https://doi.org/10.3390/molecules24234371
336. Stühn, L., Auernhammer, J., & Dietz, C. (2019). pH-depended protein shell dis- and reassembly of ferritin nanoparticles revealed by atomic force microscopy. Scientific reports, 9(1), 17755. https://doi.org/10.1038/s41598-019-53943-3
337. Ashour, A. E., Badran, M., Kumar, A., Hussain, T., Alsarra, I. A., & Yassin, A. (2019). Physical PEGylation Enhances The Cytotoxicity Of 5-Fluorouracil-Loaded PLGA And PCL Nanoparticles. International journal of nanomedicine, 14, 9259–9273. https://doi.org/10.2147/IJN.S223368
338. Hao, Y. N., Zheng, A. Q., Guo, T. T., Shu, Y., Wang, J. H., Johnson, O., & Chen, W. (2019). Glutathione triggered degradation of polydopamine to facilitate controlled drug release for synergic combinational cancer treatment. Journal of materials chemistry. B, 7(43), 6742–6750. https://doi.org/10.1039/c9tb01400d
339. Chenthamara, D., Subramaniam, S., Ramakrishnan, S. G., Krishnaswamy, S., Essa, M. M., Lin, F. H., & Qoronfleh, M. W. (2019). Therapeutic efficacy of nanoparticles and routes of administration. Biomaterials research, 23, 20. https://doi.org/10.1186/s40824-019-0166-x
340. Yan, L., Luo, L., Amirshaghaghi, A., Miller, J., Meng, C., You, T., Busch, T. M., Tsourkas, A., & Cheng, Z. (2019). Dextran-Benzoporphyrin Derivative (BPD) Coated Superparamagnetic Iron Oxide Nanoparticle (SPION) Micelles for T2-Weighted Magnetic Resonance Imaging and Photodynamic Therapy. Bioconjugate chemistry, 30(11), 2974–2981. https://doi.org/10.1021/acs.bioconjchem.9b00676
341. Bhalla, Y., Chadha, K., Chadha, R., & Karan, M. (2019). Daidzein cocrystals: An opportunity to improve its biopharmaceutical parameters. Heliyon, 5(11), e02669. https://doi.org/10.1016/j.heliyon.2019.e02669
342. d'Angelo, M., Castelli, V., Benedetti, E., Antonosante, A., Catanesi, M., Dominguez-Benot, R., Pitari, G., Ippoliti, R., & Cimini, A. (2019). Theranostic Nanomedicine for Malignant Gliomas. Frontiers in bioengineering and biotechnology, 7, 325. https://doi.org/10.3389/fbioe.2019.00325
343. Tataranni, T., & Piccoli, C. (2019). Dichloroacetate (DCA) and Cancer: An Overview towards Clinical Applications. Oxidative medicine and cellular longevity, 2019, 8201079. https://doi.org/10.1155/2019/8201079
344. Zhao, Z., Ukidve, A., Gao, Y., Kim, J., & Mitragotri, S. (2019). Erythrocyte leveraged chemotherapy (ELeCt): Nanoparticle assembly on erythrocyte surface to combat lung metastasis. Science advances, 5(11), eaax9250. https://doi.org/10.1126/sciadv.aax9250
345. Mattheolabakis, G., & Mikelis, C. M. (2019). Nanoparticle Delivery and Tumor Vascular Normalization: The Chicken or The Egg?. Frontiers in oncology, 9, 1227. https://doi.org/10.3389/fonc.2019.01227
346. Altay, Y., Cao, S., Che, H., Abdelmohsen, L., & van Hest, J. (2019). Adaptive Polymeric Assemblies for Applications in Biomimicry and Nanomedicine. Biomacromolecules, 20(11), 4053–4064. https://doi.org/10.1021/acs.biomac.9b01341
347. van der Meel, R., Sulheim, E., Shi, Y., Kiessling, F., Mulder, W., & Lammers, T. (2019). Smart cancer nanomedicine. Nature nanotechnology, 14(11), 1007–1017. https://doi.org/10.1038/s41565-019-0567-y
348. Saqr, A., Vakili, M. R., Huang, Y. H., Lai, R., & Lavasanifar, A. (2019). Development of Traceable Rituximab-Modified PEO-Polyester Micelles by Postinsertion of PEG-phospholipids for Targeting of B-cell Lymphoma. ACS omega, 4(20), 18867–18879. https://doi.org/10.1021/acsomega.9b02910
349. Loya, J., Zhang, C., Cox, E., Achrol, A. S., & Kesari, S. (2019). Biological intratumoral therapy for the high-grade glioma part II: vector- and cell-based therapies and radioimmunotherapy. CNS oncology, 8(3), CNS40. https://doi.org/10.2217/cns-2019-0002
350. Dumontel, B., Susa, F., Limongi, T., Canta, M., Racca, L., Chiodoni, A., Garino, N., Chiabotto, G., Centomo, M. L., Pignochino, Y., & Cauda, V. (2019). ZnO nanocrystals shuttled by extracellular vesicles as effective Trojan nano-horses against cancer cells. Nanomedicine (London, England), 14(21), 2815–2833. https://doi.org/10.2217/nnm-2019-0231
351. Yin, X., Luo, L., Li, W., Yang, J., Zhu, C., Jiang, M., Qin, B., Yuan, X., Yin, H., Lu, Y., Du, Y., Chen, D., & You, J. (2019). A cabazitaxel liposome for increased solubility, enhanced antitumor effect and reduced systemic toxicity. Asian journal of pharmaceutical sciences, 14(6), 658–667. https://doi.org/10.1016/j.ajps.2018.10.004
352. Lee, M. H., Liu, K. H., Thomas, J. L., Chen, J. R., & Lin, H. Y. (2019). Immunotherapy of Hepatocellular Carcinoma with Magnetic PD-1 Peptide-Imprinted Polymer Nanocomposite and Natural Killer Cells. Biomolecules, 9(11), 651. https://doi.org/10.3390/biom9110651
353. Gdowski, A. S., Lampe, J. B., Lin, V., Joshi, R., Wang, Y. C., Mukerjee, A., Vishwanatha, J. K., & Ranjan, A. P. (2019). Bioinspired Nanoparticles Engineered for Enhanced Delivery to the Bone. ACS applied nano materials, 2(10), 6249–6257. https://doi.org/10.1021/acsanm.9b01226
354. Jiang, Z., Pflug, K., Usama, S. M., Kuai, D., Yan, X., Sitcheran, R., & Burgess, K. (2019). Cyanine-Gemcitabine Conjugates as Targeted Theranostic Agents for Glioblastoma Tumor Cells. Journal of medicinal chemistry, 62(20), 9236–9245. https://doi.org/10.1021/acs.jmedchem.9b01147
355. Chen, J., Liu, J., Hu, Y., Tian, Z., & Zhu, Y. (2019). Metal-organic framework-coated magnetite nanoparticles for synergistic magnetic hyperthermia and chemotherapy with pH-triggered drug release. Science and technology of advanced materials, 20(1), 1043–1054. https://doi.org/10.1080/14686996.2019.1682467
356. Myerson, J. W., McPherson, O., DeFrates, K. G., Towslee, J. H., Marcos-Contreras, O. A., Shuvaev, V. V., Braender, B., Composto, R. J., Muzykantov, V. R., & Eckmann, D. M. (2019). Cross-linker-Modulated Nanogel Flexibility Correlates with Tunable Targeting to a Sterically Impeded Endothelial Marker. ACS nano, 13(10), 11409–11421. https://doi.org/10.1021/acsnano.9b04789
357. Levada, K., Omelyanchik, A., Rodionova, V., Weiskirchen, R., & Bartneck, M. (2019). Magnetic-Assisted Treatment of Liver Fibrosis. Cells, 8(10), 1279. https://doi.org/10.3390/cells8101279
358. Zhang, S., Guo, N., Wan, G., Zhang, T., Li, C., Wang, Y., Wang, Y., & Liu, Y. (2019). pH and redox dual-responsive nanoparticles based on disulfide-containing poly(β-amino ester) for combining chemotherapy and COX-2 inhibitor to overcome drug resistance in breast cancer. Journal of nanobiotechnology, 17(1), 109. https://doi.org/10.1186/s12951-019-0540-9
359. Xu, X., Li, T., Shen, S., Wang, J., Abdou, P., Gu, Z., & Mo, R. (2019). Advances in Engineering Cells for Cancer Immunotherapy. Theranostics, 9(25), 7889–7905. https://doi.org/10.7150/thno.38583
360. Yang, X., Xie, S., Yang, X., Cueva, J. C., Hou, X., Tang, Z., Yao, H., Mo, F., Yin, S., Liu, A., & Lu, X. (2019). Opportunities and Challenges for Antibodies against Intracellular Antigens. Theranostics, 9(25), 7792–7806. https://doi.org/10.7150/thno.35486
361. Vijayan, V., Mohapatra, A., Uthaman, S., & Park, I. K. (2019). Recent Advances in Nanovaccines Using Biomimetic Immunomodulatory Materials. Pharmaceutics, 11(10), 534. https://doi.org/10.3390/pharmaceutics11100534
362. Li, C., Yang, X. Q., An, J., Cheng, K., Hou, X. L., Zhang, X. S., Song, X. L., Huang, K. C., Chen, W., Liu, B., Zhao, Y. D., & Liu, T. C. (2019). A near-infrared light-controlled smart nanocarrier with reversible polypeptide-engineered valve for targeted fluorescence-photoacoustic bimodal imaging-guided chemo-photothermal therapy. Theranostics, 9(25), 7666–7679. https://doi.org/10.7150/thno.37047
363. Hsu, J. C., Cruz, E. D., Lau, K. C., Bouché, M., Kim, J., Maidment, A., & Cormode, D. P. (2019). Renally Excretable and Size-Tunable Silver Sulfide Nanoparticles for Dual-Energy Mammography or Computed Tomography. Chemistry of materials : a publication of the American Chemical Society, 31(19), 7845–7854. https://doi.org/10.1021/acs.chemmater.9b01750
364. Yang, L., Zhou, Z., Song, J., & Chen, X. (2019). Anisotropic nanomaterials for shape-dependent physicochemical and biomedical applications. Chemical Society reviews, 48(19), 5140–5176. https://doi.org/10.1039/c9cs00011a
365. Sansaloni-Pastor, S., Bouilloux, J., & Lange, N. (2019). The Dark Side: Photosensitizer Prodrugs. Pharmaceuticals (Basel, Switzerland), 12(4), 148. https://doi.org/10.3390/ph12040148
366. Vanderburgh, J. P., Kwakwa, K. A., Werfel, T. A., Merkel, A. R., Gupta, M. K., Johnson, R. W., Guelcher, S. A., Duvall, C. L., & Rhoades, J. A. (2019). Systemic delivery of a Gli inhibitor via polymeric nanocarriers inhibits tumor-induced bone disease. Journal of controlled release : official journal of the Controlled Release Society, 311-312, 257–272. https://doi.org/10.1016/j.jconrel.2019.08.038
367. Fu, Y., Rathod, D., Abo-Ali, E. M., Dukhande, V. V., & Patel, K. (2019). EphA2-Receptor Targeted PEGylated Nanoliposomes for the Treatment of BRAFV600E Mutated Parent- and Vemurafenib-Resistant Melanoma. Pharmaceutics, 11(10), 504. https://doi.org/10.3390/pharmaceutics11100504
368. Liu, G., Gao, N., Zhou, Y., Nie, J., Cheng, W., Luo, M., Mei, L., Zeng, X., & Deng, W. (2019). Polydopamine-Based "Four-in-One" Versatile Nanoplatforms for Targeted Dual Chemo and Photothermal Synergistic Cancer Therapy. Pharmaceutics, 11(10), 507. https://doi.org/10.3390/pharmaceutics11100507
369. Yang, B., Choi, H., Kim, S. H., Yoon, H. J., & Lee, H. (2019). How will nanotechnology lead to better control of asthma?. Annals of translational medicine, 7(20), 515. https://doi.org/10.21037/atm.2019.09.129
370. Ðorđević, L., Arcudi, F., & Prato, M. (2019). Preparation, functionalization and characterization of engineered carbon nanodots. Nature protocols, 14(10), 2931–2953. https://doi.org/10.1038/s41596-019-0207-x
371. Huang, L., Zhang, H., Wu, S., Xu, X., Zhang, L., Ji, H., He, L., Qian, Y., Wang, Z., Chen, Y., Shen, J., Mao, Z. W., & Huang, Z. (2019). Charge Regulation of Self-Assembled Tubules by Protonation for Efficiently Selective and Controlled Drug Delivery. iScience, 19, 224–231. https://doi.org/10.1016/j.isci.2019.07.030
372. Pereira, D., Cardoso, B. D., Rodrigues, A., Amorim, C. O., Amaral, V. S., Almeida, B. G., Queiroz, M., Martinho, O., Baltazar, F., Calhelha, R. C., Ferreira, I., Coutinho, P., & Castanheira, E. (2019). Magnetoliposomes Containing Calcium Ferrite Nanoparticles for Applications in Breast Cancer Therapy. Pharmaceutics, 11(9), 477. https://doi.org/10.3390/pharmaceutics11090477
373. Chen, Z., Deán-Ben, X. L., Liu, N., Gujrati, V., Gottschalk, S., Ntziachristos, V., & Razansky, D. (2019). Concurrent fluorescence and volumetric optoacoustic tomography of nanoagent perfusion and bio-distribution in solid tumors. Biomedical optics express, 10(10), 5093–5102. https://doi.org/10.1364/BOE.10.005093
374. Li, X., Wang, J., Li, S., Liu, Z., Zheng, Z., & Zhang, Y. (2019). Development and Evaluation of Multifunctional Poly(Lactic-co-glycolic acid) Nanoparticles Embedded in Carboxymethyl β-Glucan Porous Microcapsules as a Novel Drug Delivery System for Gefitinib. Pharmaceutics, 11(9), 469. https://doi.org/10.3390/pharmaceutics11090469
375. Guo, Q., He, X., Li, C., He, Y., Peng, Y., Zhang, Y., Lu, Y., Chen, X., Zhang, Y., Chen, Q., Sun, T., & Jiang, C. (2019). Dandelion-Like Tailorable Nanoparticles for Tumor Microenvironment Modulation. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(21), 1901430. https://doi.org/10.1002/advs.201901430
376. Lynn, G. M., Laga, R., & Jewell, C. M. (2019). Induction of anti-cancer T cell immunity by in situ vaccination using systemically administered nanomedicines. Cancer letters, 459, 192–203. https://doi.org/10.1016/j.canlet.2019.114427
377. Zhang, Y., Fang, Z., Li, R., Huang, X., & Liu, Q. (2019). Design of Outer Membrane Vesicles as Cancer Vaccines: A New Toolkit for Cancer Therapy. Cancers, 11(9), 1314. https://doi.org/10.3390/cancers11091314
378. Anselmo, A. C., & Mitragotri, S. (2019). Nanoparticles in the clinic: An update. Bioengineering & translational medicine, 4(3), e10143. https://doi.org/10.1002/btm2.10143
379. Chauhan, N., Maher, D. M., Hafeez, B. B., Mandil, H., Singh, M. M., Yallapu, M. M., Jaggi, M., & Chauhan, S. C. (2019). Ormeloxifene nanotherapy for cervical cancer treatment. International journal of nanomedicine, 14, 7107–7121. https://doi.org/10.2147/IJN.S200944
380. Yamashita, K., Tsunoda, S., Gunji, S., Murakami, T., Suzuki, T., Tabata, Y., & Sakai, Y. (2019). Intraperitoneal chemotherapy for peritoneal metastases using sustained release formula of cisplatin-incorporated gelatin hydrogel granules. Surgery today, 49(9), 785–794. https://doi.org/10.1007/s00595-019-01792-y
381. Kaur, G., Arora, M., & Ravi Kumar, M. (2019). Oral Drug Delivery Technologies-A Decade of Developments. The Journal of pharmacology and experimental therapeutics, 370(3), 529–543. https://doi.org/10.1124/jpet.118.255828
382. Heath, B. R., Michmerhuizen, N. L., Donnelly, C. R., Sansanaphongpricha, K., Sun, D., Brenner, J. C., & Lei, Y. L. (2019). Head and Neck Cancer Immunotherapy beyond the Checkpoint Blockade. Journal of dental research, 98(10), 1073–1080. https://doi.org/10.1177/0022034519864112
383. Zhao, X., Liu, X., Zhang, P., Liu, Y., Ran, W., Cai, Y., Wang, J., Zhai, Y., Wang, G., Ding, Y., & Li, Y. (2019). Injectable peptide hydrogel as intraperitoneal triptolide depot for the treatment of orthotopic hepatocellular carcinoma. Acta pharmaceutica Sinica. B, 9(5), 1050–1060. https://doi.org/10.1016/j.apsb.2019.06.001
384. Wei, F., Yin, C., Zheng, J., Zhan, Z., & Yao, L. (2019). Rise of cyborg microrobot: different story for different configuration. IET nanobiotechnology, 13(7), 651–664. https://doi.org/10.1049/iet-nbt.2018.5374
385. Singh, A. P., Biswas, A., Shukla, A., & Maiti, P. (2019). Targeted therapy in chronic diseases using nanomaterial-based drug delivery vehicles. Signal transduction and targeted therapy, 4, 33. https://doi.org/10.1038/s41392-019-0068-3
386. Zhuang, W., Ma, B., Hu, J., Jiang, J., Li, G., Yang, L., & Wang, Y. (2019). Two-photon AIE luminogen labeled multifunctional polymeric micelles for theranostics. Theranostics, 9(22), 6618–6630. https://doi.org/10.7150/thno.33901
387. Xu, Z., Ni, R., & Chen, Y. (2019). Targeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin. International journal of nanomedicine, 14, 6831–6842. https://doi.org/10.2147/IJN.S200482
388. Peng, C., Yu, M., Hsieh, J. T., Kapur, P., & Zheng, J. (2019). Correlating Anticancer Drug Delivery Efficiency with Vascular Permeability of Renal Clearable Versus Non-renal Clearable Nanocarriers. Angewandte Chemie (International ed. in English), 58(35), 12076–12080. https://doi.org/10.1002/anie.201905738
389. Yong, T., Zhang, X., Bie, N., Zhang, H., Zhang, X., Li, F., Hakeem, A., Hu, J., Gan, L., Santos, H. A., & Yang, X. (2019). Tumor exosome-based nanoparticles are efficient drug carriers for chemotherapy. Nature communications, 10(1), 3838. https://doi.org/10.1038/s41467-019-11718-4
390. Mohammad, O., Faisal, S. M., Ahmad, N., Rauf, M. A., Umar, M. S., Mujeeb, A. A., Pachauri, P., Ahmed, A., Kashif, M., Ajmal, M., & Zubair, S. (2019). Bio-mediated synthesis of 5-FU based nanoparticles employing orange fruit juice: a novel drug delivery system to treat skin fibrosarcoma in model animals. Scientific reports, 9(1), 12288. https://doi.org/10.1038/s41598-019-48180-7
391. Ebadi, M., Saifullah, B., Buskaran, K., Hussein, M. Z., & Fakurazi, S. (2019). Synthesis and properties of magnetic nanotheranostics coated with polyethylene glycol/5-fluorouracil/layered double hydroxide. International journal of nanomedicine, 14, 6661–6678. https://doi.org/10.2147/IJN.S214923
392. Shi, S., Wen, X., Li, T., Wen, X., Cao, Q., Liu, X., Liu, Y., Pagel, M. D., & Li, C. (2019). Thermosensitive Biodegradable Copper Sulfide Nanoparticles for Real-Time Multispectral Optoacoustic Tomography. ACS applied bio materials, 2(8), 3203–3211. https://doi.org/10.1021/acsabm.9b00133
393. Wang, Q. S., Gao, L. N., Zhu, X. N., Zhang, Y., Zhang, C. N., Xu, D., & Cui, Y. L. (2019). Co-delivery of glycyrrhizin and doxorubicin by alginate nanogel particles attenuates the activation of macrophage and enhances the therapeutic efficacy for hepatocellular carcinoma. Theranostics, 9(21), 6239–6255. https://doi.org/10.7150/thno.35972
394. Huang, P., Wang, G., Su, Y., Zhou, Y., Huang, W., Zhang, R., & Yan, D. (2019). Stimuli-responsive nanodrug self-assembled from amphiphilic drug-inhibitor conjugate for overcoming multidrug resistance in cancer treatment. Theranostics, 9(20), 5755–5768. https://doi.org/10.7150/thno.36163
395. Liu, X., Sun, Y., Xu, S., Gao, X., Kong, F., Xu, K., & Tang, B. (2019). Homotypic Cell Membrane-Cloaked Biomimetic Nanocarrier for the Targeted Chemotherapy of Hepatocellular Carcinoma. Theranostics, 9(20), 5828–5838. https://doi.org/10.7150/thno.34837
396. Abumanhal-Masarweh, H., da Silva, D., Poley, M., Zinger, A., Goldman, E., Krinsky, N., Kleiner, R., Shenbach, G., Schroeder, J. E., Shklover, J., Shainsky-Roitman, J., & Schroeder, A. (2019). Tailoring the lipid composition of nanoparticles modulates their cellular uptake and affects the viability of triple negative breast cancer cells. Journal of controlled release : official journal of the Controlled Release Society, 307, 331–341. https://doi.org/10.1016/j.jconrel.2019.06.025
397. Lakkadwala, S., Dos Santos Rodrigues, B., Sun, C., & Singh, J. (2019). Dual functionalized liposomes for efficient co-delivery of anti-cancer chemotherapeutics for the treatment of glioblastoma. Journal of controlled release : official journal of the Controlled Release Society, 307, 247–260. https://doi.org/10.1016/j.jconrel.2019.06.033
398. Kumar, R., Singh, A., & Garg, N. (2019). Acoustic Cavitation-Assisted Formulation of Solid Lipid Nanoparticles using Different Stabilizers. ACS omega, 4(8), 13360–13370. https://doi.org/10.1021/acsomega.9b01532
399. Cao, Z., Cheng, S., Wang, X., Pang, Y., & Liu, J. (2019). Camouflaging bacteria by wrapping with cell membranes. Nature communications, 10(1), 3452. https://doi.org/10.1038/s41467-019-11390-8
400. Pandya, A. D., Jäger, E., Bagheri Fam, S., Höcherl, A., Jäger, A., Sincari, V., Nyström, B., Štěpánek, P., Skotland, T., Sandvig, K., Hrubý, M., & Mælandsmo, G. M. (2019). Paclitaxel-loaded biodegradable ROS-sensitive nanoparticles for cancer therapy. International journal of nanomedicine, 14, 6269–6285. https://doi.org/10.2147/IJN.S208938
401. Yan, S., Zhao, P., Yu, T., & Gu, N. (2019). Current applications and future prospects of nanotechnology in cancer immunotherapy. Cancer biology & medicine, 16(3), 486–497. https://doi.org/10.20892/j.issn.2095-3941.2018.0493
402. Kwon, S., Yoo, K. H., Sym, S. J., & Khang, D. (2019). Mesenchymal stem cell therapy assisted by nanotechnology: a possible combinational treatment for brain tumor and central nerve regeneration. International journal of nanomedicine, 14, 5925–5942. https://doi.org/10.2147/IJN.S217923
403. Zeng, Y., Hoque, J., & Varghese, S. (2019). Biomaterial-assisted local and systemic delivery of bioactive agents for bone repair. Acta biomaterialia, 93, 152–168. https://doi.org/10.1016/j.actbio.2019.01.060
404. Navya, P. N., Kaphle, A., Srinivas, S. P., Bhargava, S. K., Rotello, V. M., & Daima, H. K. (2019). Current trends and challenges in cancer management and therapy using designer nanomaterials. Nano convergence, 6(1), 23. https://doi.org/10.1186/s40580-019-0193-2
405. Nunes, T., Pons, T., Hou, X., Van Do, K., Caron, B., Rigal, M., Di Benedetto, M., Palpant, B., Leboeuf, C., Janin, A., & Bousquet, G. (2019). Pulsed-laser irradiation of multifunctional gold nanoshells to overcome trastuzumab resistance in HER2-overexpressing breast cancer. Journal of experimental & clinical cancer research : CR, 38(1), 306. https://doi.org/10.1186/s13046-019-1305-x
406. Li, J., Gu, Y., Zhang, W., Bao, C. Y., Li, C. R., Zhang, J. Y., Liu, T., Li, S., Huang, J. X., Xie, Z. G., Hua, S. C., & Wan, Y. (2019). Molecular Mechanism for Selective Cytotoxicity towards Cancer Cells of Diselenide-Containing Paclitaxel Nanoparticles. International journal of biological sciences, 15(8), 1755–1770. https://doi.org/10.7150/ijbs.34878
407. Nik, M. E., Malaekeh-Nikouei, B., Amin, M., Hatamipour, M., Teymouri, M., Sadeghnia, H. R., Iranshahi, M., & Jaafari, M. R. (2019). Liposomal formulation of Galbanic acid improved therapeutic efficacy of pegylated liposomal Doxorubicin in mouse colon carcinoma. Scientific reports, 9(1), 9527. https://doi.org/10.1038/s41598-019-45974-7
408. Mulder, W., Ochando, J., Joosten, L., Fayad, Z. A., & Netea, M. G. (2019). Therapeutic targeting of trained immunity. Nature reviews. Drug discovery, 18(7), 553–566. https://doi.org/10.1038/s41573-019-0025-4
409. Xia, Q., Zhang, Y., Li, Z., Hou, X., & Feng, N. (2019). Red blood cell membrane-camouflaged nanoparticles: a novel drug delivery system for antitumor application. Acta pharmaceutica Sinica. B, 9(4), 675–689. https://doi.org/10.1016/j.apsb.2019.01.011
410. Soleimani, N., Vaseghi, A., & Loconte, V. (2019). Poliglusam Nanoparticles Activate T Cell Response in Breast Cancer Cell: an In Vivo and In Vitro Study. Journal of fluorescence, 29(4), 1057–1064. https://doi.org/10.1007/s10895-019-02423-y
411. Shao, Y., Luo, W., Guo, Q., Li, X., Zhang, Q., & Li, J. (2019). In vitro and in vivo effect of hyaluronic acid modified, doxorubicin and gallic acid co-delivered lipid-polymeric hybrid nano-system for leukemia therapy. Drug design, development and therapy, 13, 2043–2055. https://doi.org/10.2147/DDDT.S202818
412. Madurantakam Royam, M., Ramesh, R., Shanker, R., Sabarimurugan, S., Kumarasamy, C., Ramesh, N., Gothandam, K. M., Baxi, S., Gupta, A., Krishnan, S., & Jayaraj, R. (2019). miRNA Predictors of Pancreatic Cancer Chemotherapeutic Response: A Systematic Review and Meta-Analysis. Cancers, 11(7), 900. https://doi.org/10.3390/cancers11070900
413. Deng, H., , Dutta, P., , & Liu, J., (2019). Entry modes of ellipsoidal nanoparticles on a membrane during clathrin-mediated endocytosis. Soft matter, 15(25), 5128–5137. https://doi.org/10.1039/c9sm00751b
414. Li, Y., Dang, J., Liang, Q., & Yin, L. (2019). Thermal-Responsive Carbon Monoxide (CO) Delivery Expedites Metabolic Exhaustion of Cancer Cells toward Reversal of Chemotherapy Resistance. ACS central science, 5(6), 1044–1058. https://doi.org/10.1021/acscentsci.9b00216
415. Chen, X., Li, R., Wong, S., Wei, K., Cui, M., Chen, H., Jiang, Y., Yang, B., Zhao, P., Xu, J., Chen, H., Yin, C., Lin, S., Lee, W. Y., Jing, Y., Li, Z., Yang, Z., Xia, J., Chen, G., Li, G., … Bian, L. (2019). Conformational manipulation of scale-up prepared single-chain polymeric nanogels for multiscale regulation of cells. Nature communications, 10(1), 2705. https://doi.org/10.1038/s41467-019-10640-z
416. Shi, Y., & Lammers, T. (2019). Combining Nanomedicine and Immunotherapy. Accounts of chemical research, 52(6), 1543–1554. https://doi.org/10.1021/acs.accounts.9b00148
417. Zi, C. T., Gao, Y. S., Yang, L., Feng, S. Y., Huang, Y., Sun, L., Jin, Y., Xu, F. Q., Dong, F. W., Li, Y., Ding, Z. T., Zhou, J., Jiang, Z. H., Yuan, S. T., & Hu, J. M. (2019). Design, Synthesis, and Biological Evaluation of Novel Biotinylated Podophyllotoxin Derivatives as Potential Antitumor Agents. Frontiers in chemistry, 7, 434. https://doi.org/10.3389/fchem.2019.00434
418. Sánchez-López, E., Guerra, M., Dias-Ferreira, J., Lopez-Machado, A., Ettcheto, M., Cano, A., Espina, M., Camins, A., Garcia, M. L., & Souto, E. B. (2019). Current Applications of Nanoemulsions in Cancer Therapeutics. Nanomaterials (Basel, Switzerland), 9(6), 821. https://doi.org/10.3390/nano9060821
419. Fischer, J., Beckers, S. J., Yiamsawas, D., Thines, E., Landfester, K., & Wurm, F. R. (2019). Targeted Drug Delivery in Plants: Enzyme-Responsive Lignin Nanocarriers for the Curative Treatment of the Worldwide Grapevine Trunk Disease Esca. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(15), 1802315. https://doi.org/10.1002/advs.201802315
420. Li, Y., Zhang, T., Liu, Q., Zhang, J., Li, R., Pu, S., Wu, T., Ma, L., & He, J. (2019). Mixed micelles loaded with the 5-benzylidenethiazolidine-2,4-dione derivative SKLB023 for efficient treatment of non-alcoholic steatohepatitis. International journal of nanomedicine, 14, 3943–3953. https://doi.org/10.2147/IJN.S202821
421. Zhao, M., Cui, Y., Zhao, L., Zhu, T., Lee, R. J., Liao, W., Sun, F., Li, Y., & Teng, L. (2019). Thiophene Derivatives as New Anticancer Agents and Their Therapeutic Delivery Using Folate Receptor-Targeting Nanocarriers. ACS omega, 4(5), 8874–8880. https://doi.org/10.1021/acsomega.9b00554
422. Wang, S., Qin, L., Yamankurt, G., Skakuj, K., Huang, Z., Chen, P. C., Dominguez, D., Lee, A., Zhang, B., & Mirkin, C. A. (2019). Rational vaccinology with spherical nucleic acids. Proceedings of the National Academy of Sciences of the United States of America, 116(21), 10473–10481. https://doi.org/10.1073/pnas.1902805116
423. Lee, Y. W., Luther, D. C., Kretzmann, J. A., Burden, A., Jeon, T., Zhai, S., & Rotello, V. M. (2019). Protein Delivery into the Cell Cytosol using Non-Viral Nanocarriers. Theranostics, 9(11), 3280–3292. https://doi.org/10.7150/thno.34412
424. Li, S., Zou, Q., Xing, R., Govindaraju, T., Fakhrullin, R., & Yan, X. (2019). Peptide-modulated self-assembly as a versatile strategy for tumor supramolecular nanotheranostics. Theranostics, 9(11), 3249–3261. https://doi.org/10.7150/thno.31814
425. Hoang, N. H., Sim, T., Lim, C., Le, T. N., Han, S. M., Lee, E. S., Youn, Y. S., & Oh, K. T. (2019). A nano-sized blending system comprising identical triblock copolymers with different hydrophobicity for fabrication of an anticancer drug nanovehicle with high stability and solubilizing capacity. International journal of nanomedicine, 14, 3629–3644. https://doi.org/10.2147/IJN.S191126
426. Zhu, Y. H., Ye, N., Tang, X. F., Khan, M. I., Liu, H. L., Shi, N., & Hang, L. F. (2019). Synergistic Effect of Retinoic Acid Polymeric Micelles and Prodrug for the Pharmacodynamic Evaluation of Tumor Suppression. Frontiers in pharmacology, 10, 447. https://doi.org/10.3389/fphar.2019.00447
427. Zottel, A., Videtič Paska, A., & Jovčevska, I. (2019). Nanotechnology Meets Oncology: Nanomaterials in Brain Cancer Research, Diagnosis and Therapy. Materials (Basel, Switzerland), 12(10), 1588. https://doi.org/10.3390/ma12101588
428. Maslanka Figueroa, S., Veser, A., Abstiens, K., Fleischmann, D., Beck, S., & Goepferich, A. (2019). Influenza A virus mimetic nanoparticles trigger selective cell uptake. Proceedings of the National Academy of Sciences of the United States of America, 116(20), 9831–9836. https://doi.org/10.1073/pnas.1902563116
429. Wathiong, B., Deville, S., Jacobs, A., Smisdom, N., Gervois, P., Lambrichts, I., Ameloot, M., Hooyberghs, J., & Nelissen, I. (2019). Role of nanoparticle size and sialic acids in the distinct time-evolution profiles of nanoparticle uptake in hematopoietic progenitor cells and monocytes. Journal of nanobiotechnology, 17(1), 62. https://doi.org/10.1186/s12951-019-0495-x
430. Iturrioz-Rodríguez, N., Correa-Duarte, M. A., & Fanarraga, M. L. (2019). Controlled drug delivery systems for cancer based on mesoporous silica nanoparticles. International journal of nanomedicine, 14, 3389–3401. https://doi.org/10.2147/IJN.S198848
431. Bandyopadhyay, A., Yadav, P., Sarkar, K., & Bhattacharyya, S. (2019). The destructive spontaneous ingression of tunable silica nanosheets through cancer cell membranes. Chemical science, 10(24), 6184–6192. https://doi.org/10.1039/c9sc00076c
432. González-Ayón, M. A., Licea-Claveríe, Á., Valdez-Torres, J. B., Picos-Corrales, L. A., Vélez-de la Rocha, R., Contreras-Esquivel, J. C., Labavitch, J. M., & Sañudo-Barajas, J. A. (2019). Enzyme-Catalyzed Production of Potato Galactan-Oligosaccharides and Its Optimization by Response Surface Methodology. Materials (Basel, Switzerland), 12(9), 1465. https://doi.org/10.3390/ma12091465
433. Li, B., & Lane, L. A. (2019). Probing the biological obstacles of nanomedicine with gold nanoparticles. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 11(3), e1542. https://doi.org/10.1002/wnan.1542
434. Sahu, P., Kashaw, S. K., Sau, S., Kushwah, V., Jain, S., Agrawal, R. K., & Iyer, A. K. (2019). pH triggered and charge attracted nanogel for simultaneous evaluation of penetration and toxicity against skin cancer: In-vitro and ex-vivo study. International journal of biological macromolecules, 128, 740–751. https://doi.org/10.1016/j.ijbiomac.2019.01.147
435. Xu, C., Lei, C., & Yu, C. (2019). Mesoporous Silica Nanoparticles for Protein Protection and Delivery. Frontiers in chemistry, 7, 290. https://doi.org/10.3389/fchem.2019.00290
436. Xuan, M., Shao, J., & Li, J. (2019). Cell membrane-covered nanoparticles as biomaterials. National science review, 6(3), 551–561. https://doi.org/10.1093/nsr/nwz037
437. Akhtar, A., Ghali, L., Wang, S. X., Bell, C., Li, D., & Wen, X. (2019). Optimisation of Folate-Mediated Liposomal Encapsulated Arsenic Trioxide for Treating HPV-Positive Cervical Cancer Cells In Vitro. International journal of molecular sciences, 20(9), 2156. https://doi.org/10.3390/ijms20092156
438. Wang, Y., Zhang, K., Qin, X., Li, T., Qiu, J., Yin, T., Huang, J., McGinty, S., Pontrelli, G., Ren, J., Wang, Q., Wu, W., & Wang, G. (2019). Biomimetic Nanotherapies: Red Blood Cell Based Core-Shell Structured Nanocomplexes for Atherosclerosis Management. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(12), 1900172. https://doi.org/10.1002/advs.201900172
439. Vankayala, R., , Mac, J. T., , Burns, J. M., , Dunn, E., , Carroll, S., , Bahena, E. M., , Patel, D. K., , Griffey, S., , & Anvari, B., (2019). Biodistribution and toxicological evaluation of micron- and nano-sized erythrocyte-derived optical particles in healthy Swiss Webster mice. Biomaterials science, 7(5), 2123–2133. https://doi.org/10.1039/c8bm01448e
440. Alvaradejo, G. G., Nguyen, H. V., Harvey, P., Gallagher, N. M., Le, D., Ottaviani, M. F., Jasanoff, A., Delaittre, G., & Johnson, J. A. (2019). Polyoxazoline-Based Bottlebrush and Brush-Arm Star Polymers via ROMP: Syntheses and Applications as Organic Radical Contrast Agents. ACS macro letters, 8(4), 473–478. https://doi.org/10.1021/acsmacrolett.9b00016
441. Busatto, S., Pham, A., Suh, A., Shapiro, S., & Wolfram, J. (2019). Organotropic drug delivery: Synthetic nanoparticles and extracellular vesicles. Biomedical microdevices, 21(2), 46. https://doi.org/10.1007/s10544-019-0396-7
442. Zhang, Q., Chen, J., Shen, J., Chen, S., Liang, K., Wang, H., & Chen, H. (2019). Inlaying Radiosensitizer onto the Polypeptide Shell of Drug-Loaded Ferritin for Imaging and Combinational Chemo-Radiotherapy. Theranostics, 9(10), 2779–2790. https://doi.org/10.7150/thno.33472
443. Nguyen, V. P., Li, Y., Qian, W., Liu, B., Tian, C., Zhang, W., Huang, Z., Ponduri, A., Tarnowski, M., Wang, X., & Paulus, Y. M. (2019). Contrast Agent Enhanced Multimodal Photoacoustic Microscopy and Optical Coherence Tomography for Imaging of Rabbit Choroidal and Retinal Vessels in vivo. Scientific reports, 9(1), 5945. https://doi.org/10.1038/s41598-019-42324-5
444. Xia, K. K., Lyu, Y., Yuan, W. T., Wang, G. X., Stratton, H., Zhang, S. J., & Wu, J. (2019). Nanocarriers of Fe3O4 as a Novel Method for Delivery of the Antineoplastic Agent Doxorubicin Into HeLa Cells in vitro. Frontiers in oncology, 9, 250. https://doi.org/10.3389/fonc.2019.00250
445. Farokhirad, S., , Ranganathan, A., , Myerson, J., , Muzykantov, V. R., , Ayyaswamy, P. S., , Eckmann, D. M., , & Radhakrishnan, R., (2019). Stiffness can mediate balance between hydrodynamic forces and avidity to impact the targeting of flexible polymeric nanoparticles in flow. Nanoscale, 11(14), 6916–6928. https://doi.org/10.1039/c8nr09594a
446. Wallyn, J., Anton, N., Akram, S., & Vandamme, T. F. (2019). Biomedical Imaging: Principles, Technologies, Clinical Aspects, Contrast Agents, Limitations and Future Trends in Nanomedicines. Pharmaceutical research, 36(6), 78. https://doi.org/10.1007/s11095-019-2608-5
447. Tyo, K. M., Minooei, F., Curry, K. C., NeCamp, S. M., Graves, D. L., Fried, J. R., & Steinbach-Rankins, J. M. (2019). Relating Advanced Electrospun Fiber Architectures to the Temporal Release of Active Agents to Meet the Needs of Next-Generation Intravaginal Delivery Applications. Pharmaceutics, 11(4), 160. https://doi.org/10.3390/pharmaceutics11040160
448. Zheng, T., Feng, H., Liu, L., Peng, J., Xiao, H., Yu, T., Zhou, Z., Li, Y., Zhang, Y., Bai, X., Zhao, S., Shi, Y., & Chen, Y. (2019). Enhanced antiproliferative effect of resveratrol in head and neck squamous cell carcinoma using GE11 peptide conjugated liposome. International journal of molecular medicine, 43(4), 1635–1642. https://doi.org/10.3892/ijmm.2019.4096
449. Liyanage, P. Y., Hettiarachchi, S. D., Zhou, Y., Ouhtit, A., Seven, E. S., Oztan, C. Y., Celik, E., & Leblanc, R. M. (2019). Nanoparticle-mediated targeted drug delivery for breast cancer treatment. Biochimica et biophysica acta. Reviews on cancer, 1871(2), 419–433. https://doi.org/10.1016/j.bbcan.2019.04.006
450. DuRoss, A. N., Neufeld, M. J., Rana, S., Thomas, C. R., Jr, & Sun, C. (2019). Integrating nanomedicine into clinical radiotherapy regimens. Advanced drug delivery reviews, 144, 35–56. https://doi.org/10.1016/j.addr.2019.07.002
451. Ben-David-Naim, M., Dagan, A., Grad, E., Aizik, G., Nordling-David, M. M., Morss Clyne, A., Granot, Z., & Golomb, G. (2019). Targeted siRNA Nanoparticles for Mammary Carcinoma Therapy. Cancers, 11(4), 442. https://doi.org/10.3390/cancers11040442
452. Hettiarachchi, S. D., , Graham, R. M., , Mintz, K. J., , Zhou, Y., , Vanni, S., , Peng, Z., , & Leblanc, R. M., (2019). Triple conjugated carbon dots as a nano-drug delivery model for glioblastoma brain tumors. Nanoscale, 11(13), 6192–6205. https://doi.org/10.1039/c8nr08970a
453. Martinelli, C., Pucci, C., & Ciofani, G. (2019). Nanostructured carriers as innovative tools for cancer diagnosis and therapy. APL bioengineering, 3(1), 011502. https://doi.org/10.1063/1.5079943
454. Ganugula, R., Deng, M., Arora, M., Pan, H. L., & Kumar, M. (2019). Polyester Nanoparticle Encapsulation Mitigates Paclitaxel-Induced Peripheral Neuropathy. ACS chemical neuroscience, 10(3), 1801–1812. https://doi.org/10.1021/acschemneuro.8b00703
455. Lim, J. M., Cai, T., Mandaric, S., Chopra, S., Han, H., Jang, S., Il Choi, W., Langer, R., Farokhzad, O. C., & Karnik, R. (2019). Drug loading augmentation in polymeric nanoparticles using a coaxial turbulent jet mixer: Yong investigator perspective. Journal of colloid and interface science, 538, 45–50. https://doi.org/10.1016/j.jcis.2018.11.029
456. Gujrati, V., Prakash, J., Malekzadeh-Najafabadi, J., Stiel, A., Klemm, U., Mettenleiter, G., Aichler, M., Walch, A., & Ntziachristos, V. (2019). Bioengineered bacterial vesicles as biological nano-heaters for optoacoustic imaging. Nature communications, 10(1), 1114. https://doi.org/10.1038/s41467-019-09034-y
457. He, W., Wang, S., Yan, J., Qu, Y., Jin, L., Sui, F., Li, Y., You, W., Yang, G., Yang, Q., Ji, M., Shao, Y., Ma, P. X., Lu, W., & Hou, P. (2019). Self-Assembly of Therapeutic Peptide into Stimuli-Responsive Clustered Nanohybrids for Cancer-Targeted Therapy. Advanced functional materials, 29(10), 1807736. https://doi.org/10.1002/adfm.201807736
458. Saha Ray, A., Ghann, W. E., Tsoi, P. S., Szychowski, B., Dockery, L. T., Pak, Y. J., Li, W., Kane, M. A., Swaan, P., & Daniel, M. C. (2019). Set of Highly Stable Amine- and Carboxylate-Terminated Dendronized Au Nanoparticles with Dense Coating and Nontoxic Mixed-Dendronized Form. Langmuir : the ACS journal of surfaces and colloids, 35(9), 3391–3403. https://doi.org/10.1021/acs.langmuir.8b03196
459. Simon, A. T., Dutta, D., Chattopadhyay, A., & Ghosh, S. S. (2019). Copper Nanocluster-Doped Luminescent Hydroxyapatite Nanoparticles for Antibacterial and Antibiofilm Applications. ACS omega, 4(3), 4697–4706. https://doi.org/10.1021/acsomega.8b03076
460. Jones, S. J., Taylor, A. F., & Beales, P. A. (2019). Towards feedback-controlled nanomedicines for smart, adaptive delivery. Experimental biology and medicine (Maywood, N.J.), 244(4), 283–293. https://doi.org/10.1177/1535370218800456
461. Yanagihara, K., Kubo, T., Mihara, K., Kuwata, T., Ochiai, A., Seyama, T., & Yokozaki, H. (2019). Development and Biological Analysis of a Novel Orthotopic Peritoneal Dissemination Mouse Model Generated Using a Pancreatic Ductal Adenocarcinoma Cell Line. Pancreas, 48(3), 315–322. https://doi.org/10.1097/MPA.0000000000001253
462. Maksimović-Ivanić, D., Bulatović, M., Edeler, D., Bensing, C., Golić, I., Korać, A., Kaluđerović, G. N., & Mijatović, S. (2019). The interaction between SBA-15 derivative loaded with Ph3Sn(CH2)6OH and human melanoma A375 cell line: uptake and stem phenotype loss. Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 24(2), 223–234. https://doi.org/10.1007/s00775-019-01640-x
463. Liu, X., Wang, B., Li, Y., Hu, Y., Li, X., Yu, T., Ju, Y., Sun, T., Gao, X., & Wei, Y. (2019). Powerful Anticolon Tumor Effect of Targeted Gene Immunotherapy Using Folate-Modified Nanoparticle Delivery of CCL19 To Activate the Immune System. ACS central science, 5(2), 277–289. https://doi.org/10.1021/acscentsci.8b00688
464. Estabrook, D. A., Ennis, A. F., Day, R. A., & Sletten, E. M. (2019). Controlling nanoemulsion surface chemistry with poly(2-oxazoline) amphiphiles. Chemical science, 10(14), 3994–4003. https://doi.org/10.1039/c8sc05735d
465. Gardinier, T. C., Kohle, F., Peerless, J. S., Ma, K., Turker, M. Z., Hinckley, J. A., Yingling, Y. G., & Wiesner, U. (2019). High-Performance Chromatographic Characterization of Surface Chemical Heterogeneities of Fluorescent Organic-Inorganic Hybrid Core-Shell Silica Nanoparticles. ACS nano, 13(2), 1795–1804. https://doi.org/10.1021/acsnano.8b07876
466. Sun, J. G., Jiang, Q., Zhang, X. P., Shan, K., Liu, B. H., Zhao, C., & Yan, B. (2019). Mesoporous silica nanoparticles as a delivery system for improving antiangiogenic therapy. International journal of nanomedicine, 14, 1489–1501. https://doi.org/10.2147/IJN.S195504
467. Huang, Y. H., Vakili, M. R., Molavi, O., Morrissey, Y., Wu, C., Paiva, I., Soleimani, A. H., Sanaee, F., Lavasanifar, A., & Lai, R. (2019). Decoration of Anti-CD38 on Nanoparticles Carrying a STAT3 Inhibitor Can Improve the Therapeutic Efficacy Against Myeloma. Cancers, 11(2), 248. https://doi.org/10.3390/cancers11020248
468. Foster, J. C., Carrazzone, R. J., Spear, N. J., Radzinski, S. C., Arrington, K. J., & Matson, J. B. (2019). Tuning H2S Release by Controlling Mobility in a Micelle Core. Macromolecules, 52(3), 1104–1111. https://doi.org/10.1021/acs.macromol.8b02315
469. Mo, L., Zhao, Z., Hu, X., Yu, X., Peng, Y., Liu, H., Xiong, M., Fu, T., Jiang, Y., Zhang, X., & Tan, W. (2019). Smart Nanodrug with Nuclear Localization Sequences in the Presence of MMP-2 To Overcome Biobarriers and Drug Resistance. Chemistry (Weinheim an der Bergstrasse, Germany), 25(8), 1895–1900. https://doi.org/10.1002/chem.201805107
470. Sexton, R. E., Mpilla, G., Kim, S., Philip, P. A., & Azmi, A. S. (2019). Ras and exosome signaling. Seminars in cancer biology, 54, 131–137. https://doi.org/10.1016/j.semcancer.2019.02.004
471. Elkassih, S. A., , Kos, P., , Xiong, H., , & Siegwart, D. J., (2019). Degradable redox-responsive disulfide-based nanogel drug carriers via dithiol oxidation polymerization. Biomaterials science, 7(2), 607–617. https://doi.org/10.1039/c8bm01120f
472. Satpathy, M., Wang, L., Zielinski, R. J., Qian, W., Wang, Y. A., Mohs, A. M., Kairdolf, B. A., Ji, X., Capala, J., Lipowska, M., Nie, S., Mao, H., & Yang, L. (2019). Targeted Drug Delivery and Image-Guided Therapy of Heterogeneous Ovarian Cancer Using HER2-Targeted Theranostic Nanoparticles. Theranostics, 9(3), 778–795. https://doi.org/10.7150/thno.29964
473. Ferdinandus, & Arai, S. (2019). The ABC Guide to Fluorescent Toolsets for the Development of Future Biomaterials. Frontiers in bioengineering and biotechnology, 7, 5. https://doi.org/10.3389/fbioe.2019.00005
474. Ling, X., Tu, J., Wang, J., Shajii, A., Kong, N., Feng, C., Zhang, Y., Yu, M., Xie, T., Bharwani, Z., Aljaeid, B. M., Shi, B., Tao, W., & Farokhzad, O. C. (2019). Glutathione-Responsive Prodrug Nanoparticles for Effective Drug Delivery and Cancer Therapy. ACS nano, 13(1), 357–370. https://doi.org/10.1021/acsnano.8b06400
475. Chen, Y., Liu, X., Yuan, H., Yang, Z., von Roemeling, C. A., Qie, Y., Zhao, H., Wang, Y., Jiang, W., & Kim, B. (2019). Therapeutic Remodeling of the Tumor Microenvironment Enhances Nanoparticle Delivery. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(5), 1802070. https://doi.org/10.1002/advs.201802070
476. Wang, S., Wang, Z., Yu, G., Zhou, Z., Jacobson, O., Liu, Y., Ma, Y., Zhang, F., Chen, Z. Y., & Chen, X. (2019). Tumor-Specific Drug Release and Reactive Oxygen Species Generation for Cancer Chemo/Chemodynamic Combination Therapy. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(5), 1801986. https://doi.org/10.1002/advs.201801986
477. Pinguet, C. E., Ryll, E., Steinschulte, A. A., Hoffmann, J. M., Brugnoni, M., Sybachin, A., Wöll, D., Yaroslavov, A., Richtering, W., & Plamper, F. A. (2019). PEO-b-PPO star-shaped polymers enhance the structural stability of electrostatically coupled liposome/polyelectrolyte complexes. PloS one, 14(1), e0210898. https://doi.org/10.1371/journal.pone.0210898
478. Caffery, B., Lee, J. S., & Alexander-Bryant, A. A. (2019). Vectors for Glioblastoma Gene Therapy: Viral & Non-Viral Delivery Strategies. Nanomaterials (Basel, Switzerland), 9(1), 105. https://doi.org/10.3390/nano9010105
479. Ghosh, S., Qi, R., Carter, K. A., Zhang, G., Pfeifer, B. A., & Lovell, J. F. (2019). Loading and Releasing Ciprofloxacin in Photoactivatable Liposomes. Biochemical engineering journal, 141, 43–48. https://doi.org/10.1016/j.bej.2018.10.008
480. Mi, Y., Hagan, C. T., 4th, Vincent, B. G., & Wang, A. Z. (2019). Emerging Nano-/Microapproaches for Cancer Immunotherapy. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(6), 1801847. https://doi.org/10.1002/advs.201801847
481. Lunova, M., Smolková, B., Lynnyk, A., Uzhytchak, M., Jirsa, M., Kubinová, Š., Dejneka, A., & Lunov, O. (2019). Targeting the mTOR Signaling Pathway Utilizing Nanoparticles: A Critical Overview. Cancers, 11(1), 82. https://doi.org/10.3390/cancers11010082
482. Maziukiewicz, D., Grześkowiak, B. F., Coy, E., Jurga, S., & Mrówczyński, R. (2019). NDs@PDA@ICG Conjugates for Photothermal Therapy of Glioblastoma Multiforme. Biomimetics (Basel, Switzerland), 4(1), 3. https://doi.org/10.3390/biomimetics4010003
483. Song, C., Lin, T., Zhang, Q., Thayumanavan, S., & Ren, L. (2019). pH-Sensitive morphological transitions in polymeric tadpole assemblies for programmed tumor therapy. Journal of controlled release : official journal of the Controlled Release Society, 293, 1–9. https://doi.org/10.1016/j.jconrel.2018.10.033
484. Jang, J. D., Do, C., Bang, J., Han, Y. S., & Kim, T. H. (2019). Self-Assembly of Temperature Sensitive Unilamellar Vesicles by a Blend of Block Copolymers in Aqueous Solution. Polymers, 11(1), 63. https://doi.org/10.3390/polym11010063
485. Sun, Q., , Barz, M., , De Geest, B. G., , Diken, M., , Hennink, W. E., , Kiessling, F., , Lammers, T., , & Shi, Y., (2019). Nanomedicine and macroscale materials in immuno-oncology. Chemical Society reviews, 48(1), 351–381. https://doi.org/10.1039/c8cs00473k
486. Lakkadwala, S., & Singh, J. (2019). Co-delivery of doxorubicin and erlotinib through liposomal nanoparticles for glioblastoma tumor regression using an in vitro brain tumor model. Colloids and surfaces. B, Biointerfaces, 173, 27–35. https://doi.org/10.1016/j.colsurfb.2018.09.047
487. Starling, B. R., Kumar, P., Lucas, A. T., Barrow, D., Farnan, L., Hendrix, L., Giovinazzo, H., Song, G., Gehrig, P., Bensen, J. T., & Zamboni, W. C. (2019). Mononuclear phagocyte system function and nanoparticle pharmacology in obese and normal weight ovarian and endometrial cancer patients. Cancer chemotherapy and pharmacology, 83(1), 61–70. https://doi.org/10.1007/s00280-018-3702-9
488. Lopez-Campos, F., Candini, D., Carrasco, E., & Berenguer Francés, M. A. (2019). Nanoparticles applied to cancer immunoregulation. Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology, 24(1), 47–55. https://doi.org/10.1016/j.rpor.2018.10.001
489. Cheng, Y., Ou, Z., Li, Q., Yang, J., Hu, M., Zhou, Y., Zhuang, X., Zhang, Z. J., & Guan, S. (2019). Cabazitaxel liposomes with aptamer modification enhance tumor‑targeting efficacy in nude mice. Molecular medicine reports, 19(1), 490–498. https://doi.org/10.3892/mmr.2018.9689
490. Morales-Orue, I., Chicas-Sett, R., & Lara, P. C. (2019). Nanoparticles as a promising method to enhance the abscopal effect in the era of new targeted therapies. Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology, 24(1), 86–91. https://doi.org/10.1016/j.rpor.2018.11.001
491. Benchimol, M. J., Bourne, D., Moghimi, S. M., & Simberg, D. (2019). Pharmacokinetic analysis reveals limitations and opportunities for nanomedicine targeting of endothelial and extravascular compartments of tumours. Journal of drug targeting, 27(5-6), 690–698. https://doi.org/10.1080/1061186X.2019.1566339
492. Ravindran Girija, A., & Balasubramanian, S. (2019). Theragnostic potentials of core/shell mesoporous silica nanostructures. Nanotheranostics, 3(1), 1–40. https://doi.org/10.7150/ntno.27877
493. Ghosn, Y., Kamareddine, M. H., Tawk, A., Elia, C., El Mahmoud, A., Terro, K., El Harake, N., El-Baba, B., Makdessi, J., & Farhat, S. (2019). Inorganic Nanoparticles as Drug Delivery Systems and Their Potential Role in the Treatment of Chronic Myelogenous Leukaemia. Technology in cancer research & treatment, 18, 1533033819853241. https://doi.org/10.1177/1533033819853241
494. Wieland, K., Ramer, G., Weiss, V. U., Allmaier, G., Lendl, B., & Centrone, A. (2019). Nanoscale Chemical Imaging of Individual, Chemotherapeutic Cytarabine-loaded Liposomal Nanocarriers. Nano research, 12, 10.1007/s12274-018-2202-x. https://doi.org/10.1007/s12274-018-2202-x
495. Radhakrishnan, R., Farokhirad, S., Eckmann, D. M., & Ayyaswamy, P. S. (2019). Nanoparticle transport phenomena in confined flows. Advances in heat transfer, 51, 55–129. https://doi.org/10.1016/bs.aiht.2019.08.002
496. Hussein Kamareddine, M., Ghosn, Y., Tawk, A., Elia, C., Alam, W., Makdessi, J., & Farhat, S. (2019). Organic Nanoparticles as Drug Delivery Systems and Their Potential Role in the Treatment of Chronic Myeloid Leukemia. Technology in cancer research & treatment, 18, 1533033819879902. https://doi.org/10.1177/1533033819879902
497. Giuliano, E., Paolino, D., Fresta, M., & Cosco, D. (2018). Drug-Loaded Biocompatible Nanocarriers Embedded in Poloxamer 407 Hydrogels as Therapeutic Formulations. Medicines (Basel, Switzerland), 6(1), 7. https://doi.org/10.3390/medicines6010007
498. Aung, W., Tsuji, A. B., Sugyo, A., Takashima, H., Yasunaga, M., Matsumura, Y., & Higashi, T. (2018). Near-infrared photoimmunotherapy of pancreatic cancer using an indocyanine green-labeled anti-tissue factor antibody. World journal of gastroenterology, 24(48), 5491–5504. https://doi.org/10.3748/wjg.v24.i48.5491
499. Tang, H., Zhao, W., Yu, J., Li, Y., & Zhao, C. (2018). Recent Development of pH-Responsive Polymers for Cancer Nanomedicine. Molecules (Basel, Switzerland), 24(1), 4. https://doi.org/10.3390/molecules24010004
500. Cirri, M., Maestrelli, F., Mura, P., Ghelardini, C., & Di Cesare Mannelli, L. (2018). Combined Approach of Cyclodextrin Complexationand Nanostructured Lipid Carriers for the Development of a Pediatric Liquid Oral Dosage Form of Hydrochlorothiazide. Pharmaceutics, 10(4), 287. https://doi.org/10.3390/pharmaceutics10040287
501. Dai, L., Li, X., Duan, X., Li, M., Niu, P., Xu, H., Cai, K., & Yang, H. (2018). A pH/ROS Cascade-Responsive Charge-Reversal Nanosystem with Self-Amplified Drug Release for Synergistic Oxidation-Chemotherapy. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(4), 1801807. https://doi.org/10.1002/advs.201801807
502. Viseu, T., Lopes, C. M., Fernandes, E., Oliveira, M., & Lúcio, M. (2018). A Systematic Review and Critical Analysis of the Role of Graphene-Based Nanomaterialsin Cancer Theranostics. Pharmaceutics, 10(4), 282. https://doi.org/10.3390/pharmaceutics10040282
503. Nunes, T., Hamdan, D., Leboeuf, C., El Bouchtaoui, M., Gapihan, G., Nguyen, T. T., Meles, S., Angeli, E., Ratajczak, P., Lu, H., Di Benedetto, M., Bousquet, G., & Janin, A. (2018). Targeting Cancer Stem Cells to Overcome Chemoresistance. International journal of molecular sciences, 19(12), 4036. https://doi.org/10.3390/ijms19124036
504. Han, Y., Liu, W., Huang, J., Qiu, S., Zhong, H., Liu, D., & Liu, J. (2018). Cyclodextrin-Based Metal-Organic Frameworks (CD-MOFs) in Pharmaceutics and Biomedicine. Pharmaceutics, 10(4), 271. https://doi.org/10.3390/pharmaceutics10040271
505. Kanubaddi, K. R., Yang, S. H., Wu, L. W., Lee, C. H., & Weng, C. F. (2018). Nanoparticle-conjugated nutraceuticals exert prospectively palliative of amyloid aggregation. International journal of nanomedicine, 13, 8473–8485. https://doi.org/10.2147/IJN.S179484
506. Xu, J., Lee, S. S., Seo, H., Pang, L., Jun, Y., Zhang, R. Y., Zhang, Z. Y., Kim, P., Lee, W., Kron, S. J., & Yeo, Y. (2018). Quinic Acid-Conjugated Nanoparticles Enhance Drug Delivery to Solid Tumors via Interactions with Endothelial Selectins. Small (Weinheim an der Bergstrasse, Germany), 14(50), e1803601. https://doi.org/10.1002/smll.201803601
507. Hiremath, C. G., Kariduraganavar, M. Y., & Hiremath, M. B. (2018). Synergistic delivery of 5-fluorouracil and curcumin using human serum albumin-coated iron oxide nanoparticles by folic acid targeting. Progress in biomaterials, 7(4), 297–306. https://doi.org/10.1007/s40204-018-0104-3
508. Kulshrestha, S., & Khan, A. U. (2018). Nanomedicine for anticancer and antimicrobial treatment: an overview. IET nanobiotechnology, 12(8), 1009–1017. https://doi.org/10.1049/iet-nbt.2018.5112
509. Ray, S., Li, Z., Hsu, C. H., Hwang, L. P., Lin, Y. C., Chou, P. T., & Lin, Y. Y. (2018). Dendrimer- and copolymer-based nanoparticles for magnetic resonance cancer theranostics. Theranostics, 8(22), 6322–6349. https://doi.org/10.7150/thno.27828
510. Yu, Z., Zhou, P., Pan, W., Li, N., & Tang, B. (2018). A biomimetic nanoreactor for synergistic chemiexcited photodynamic therapy and starvation therapy against tumor metastasis. Nature communications, 9(1), 5044. https://doi.org/10.1038/s41467-018-07197-8
511. Cao, S., Abdelmohsen, L., Shao, J., van den Dikkenberg, J., Mastrobattista, E., Williams, D. S., & van Hest, J. (2018). pH-Induced Transformation of Biodegradable Multilamellar Nanovectors for Enhanced Tumor Penetration. ACS macro letters, 7(11), 1394–1399. https://doi.org/10.1021/acsmacrolett.8b00807
512. Seidler, C., Zegota, M. M., Raabe, M., Kuan, S. L., Ng, D., & Weil, T. (2018). Dynamic Core-Shell Bioconjugates for Targeted Protein Delivery and Release. Chemistry, an Asian journal, 13(22), 3474–3479. https://doi.org/10.1002/asia.201800843
513. Zhou, Y., Zhen, M., Guan, M., Yu, T., Ma, L., Li, W., Zheng, J., Shu, C., & Wang, C. (2018). Amino acid modified [70] fullerene derivatives with high radical scavenging activity as promising bodyguards for chemotherapy protection. Scientific reports, 8(1), 16573. https://doi.org/10.1038/s41598-018-34967-7
514. Xin, C., Yao, X., Du, B., Yang, W., Wang, L., Ma, L., & Weng, W. (2018). Stearic Acid-Grafted Chitooligosaccharide Nanomicelle System with Biocleavable Gadolinium Chelates as a Multifunctional Agent for Tumor Imaging and Drug Delivery. Pharmaceutical research, 36(1), 10. https://doi.org/10.1007/s11095-018-2530-2
515. Tao, S. C., Rui, B. Y., Wang, Q. Y., Zhou, D., Zhang, Y., & Guo, S. C. (2018). Extracellular vesicle-mimetic nanovesicles transport LncRNA-H19 as competing endogenous RNA for the treatment of diabetic wounds. Drug delivery, 25(1), 241–255. https://doi.org/10.1080/10717544.2018.1425774
516. Ma, B., He, L., You, Y., Mo, J., & Chen, T. (2018). Controlled synthesis and size effects of multifunctional mesoporous silica nanosystem for precise cancer therapy. Drug delivery, 25(1), 293–306. https://doi.org/10.1080/10717544.2018.1425779
517. Zhang, B., Cheng, G., Zheng, M., Han, J., Wang, B., Li, M., Chen, J., Xiao, T., Zhang, J., Cai, L., Li, S., & Fan, X. (2018). Targeted delivery of doxorubicin by CSA-binding nanoparticles for choriocarcinoma treatment. Drug delivery, 25(1), 461–471. https://doi.org/10.1080/10717544.2018.1435750
518. Su, C. Y., Chen, M., Chen, L. C., Ho, Y. S., Ho, H. O., Lin, S. Y., Chuang, K. H., & Sheu, M. T. (2018). Bispecific antibodies (anti-mPEG/anti-HER2) for active tumor targeting of docetaxel (DTX)-loaded mPEGylated nanocarriers to enhance the chemotherapeutic efficacy of HER2-overexpressing tumors. Drug delivery, 25(1), 1066–1079. https://doi.org/10.1080/10717544.2018.1466936
519. Sim, T., Kim, J. E., Hoang, N. H., Kang, J. K., Lim, C., Kim, D. S., Lee, E. S., Youn, Y. S., Choi, H. G., Han, H. K., Weon, K. Y., & Oh, K. T. (2018). Development of a docetaxel micellar formulation using poly(ethylene glycol)-polylactide-poly(ethylene glycol) (PEG-PLA-PEG) with successful reconstitution for tumor targeted drug delivery. Drug delivery, 25(1), 1362–1371. https://doi.org/10.1080/10717544.2018.1477865
520. Veloso, D., Benedetti, N., Ávila, R. I., Bastos, T., Silva, T. C., Silva, M., Batista, A. C., Valadares, M. C., & Lima, E. M. (2018). Intravenous delivery of a liposomal formulation of voriconazole improves drug pharmacokinetics, tissue distribution, and enhances antifungal activity. Drug delivery, 25(1), 1585–1594. https://doi.org/10.1080/10717544.2018.1492046
521. Lakkadwala, S., & Singh, J. (2018). Dual Functionalized 5-Fluorouracil Liposomes as Highly Efficient Nanomedicine for Glioblastoma Treatment as Assessed in an In Vitro Brain Tumor Model. Journal of pharmaceutical sciences, 107(11), 2902–2913. https://doi.org/10.1016/j.xphs.2018.07.020
522. Bahmani, B., Uehara, M., Jiang, L., Ordikhani, F., Banouni, N., Ichimura, T., Solhjou, Z., Furtmüller, G. J., Brandacher, G., Alvarez, D., von Andrian, U. H., Uchimura, K., Xu, Q., Vohra, I., Yilmam, O. A., Haik, Y., Azzi, J., Kasinath, V., Bromberg, J. S., McGrath, M. M., … Abdi, R. (2018). Targeted delivery of immune therapeutics to lymph nodes prolongs cardiac allograft survival. The Journal of clinical investigation, 128(11), 4770–4786. https://doi.org/10.1172/JCI120923
523. Figarol, A., Gibot, L., Golzio, M., Lonetti, B., Mingotaud, A. F., & Rols, M. P. (2018). A journey from the endothelium to the tumor tissue: distinct behavior between PEO-PCL micelles and polymersomes nanocarriers. Drug delivery, 25(1), 1766–1778. https://doi.org/10.1080/10717544.2018.1510064
524. Jiang, D., Ge, Z., Im, H. J., England, C. G., Ni, D., Hou, J., Zhang, L., Kutyreff, C. J., Yan, Y., Liu, Y., Cho, S. Y., Engle, J. W., Shi, J., Huang, P., Fan, C., Yan, H., & Cai, W. (2018). DNA origami nanostructures can exhibit preferential renal uptake and alleviate acute kidney injury. Nature biomedical engineering, 2(11), 865–877. https://doi.org/10.1038/s41551-018-0317-8
525. Ioannidis, J., Kim, B., & Trounson, A. (2018). How to design preclinical studies in nanomedicine and cell therapy to maximize the prospects of clinical translation. Nature biomedical engineering, 2(11), 797–809. https://doi.org/10.1038/s41551-018-0314-y
526. Arora, K., Herroon, M., Al-Afyouni, M. H., Toupin, N. P., Rohrabaugh, T. N., Jr, Loftus, L. M., Podgorski, I., Turro, C., & Kodanko, J. J. (2018). Catch and Release Photosensitizers: Combining Dual-Action Ruthenium Complexes with Protease Inactivation for Targeting Invasive Cancers. Journal of the American Chemical Society, 140(43), 14367–14380. https://doi.org/10.1021/jacs.8b08853
527. Oh, J. Y., Kim, H. S., Palanikumar, L., Go, E. M., Jana, B., Park, S. A., Kim, H. Y., Kim, K., Seo, J. K., Kwak, S. K., Kim, C., Kang, S., & Ryu, J. H. (2018). Cloaking nanoparticles with protein corona shield for targeted drug delivery. Nature communications, 9(1), 4548. https://doi.org/10.1038/s41467-018-06979-4
528. Durchschein, C., Hufner, A., Rinner, B., Stallinger, A., Deutsch, A., Lohberger, B., Bauer, R., & Kretschmer, N. (2018). Synthesis of Novel Shikonin Derivatives and Pharmacological Effects of Cyclopropylacetylshikonin on Melanoma Cells. Molecules (Basel, Switzerland), 23(11), 2820. https://doi.org/10.3390/molecules23112820
529. Kretschmer, N., Deutsch, A., Durchschein, C., Rinner, B., Stallinger, A., Higareda-Almaraz, J. C., Scheideler, M., Lohberger, B., & Bauer, R. (2018). Comparative Gene Expression Analysis in WM164 Melanoma Cells Revealed That β-β-Dimethylacrylshikonin Leads to ROS Generation, Loss of Mitochondrial Membrane Potential, and Autophagy Induction. Molecules (Basel, Switzerland), 23(11), 2823. https://doi.org/10.3390/molecules23112823
530. Song, X. R., Li, S. H., Guo, H., You, W., Tu, D., Li, J., Lu, C. H., Yang, H. H., & Chen, X. (2018). Enhancing Antitumor Efficacy by Simultaneous ATP-Responsive Chemodrug Release and Cancer Cell Sensitization Based on a Smart Nanoagent. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 5(12), 1801201. https://doi.org/10.1002/advs.201801201
531. Bai, D. P., Lin, X. Y., Huang, Y. F., & Zhang, X. F. (2018). Theranostics Aspects of Various Nanoparticles in Veterinary Medicine. International journal of molecular sciences, 19(11), 3299. https://doi.org/10.3390/ijms19113299
532. Ding, H., Li, J., Chen, N., Hu, X., Yang, X., Guo, L., Li, Q., Zuo, X., Wang, L., Ma, Y., & Fan, C. (2018). DNA Nanostructure-Programmed Like-Charge Attraction at the Cell-Membrane Interface. ACS central science, 4(10), 1344–1351. https://doi.org/10.1021/acscentsci.8b00383
533. Zhou, H., Fan, Z., Li, P. Y., Deng, J., Arhontoulis, D. C., Li, C. Y., Bowne, W. B., & Cheng, H. (2018). Dense and Dynamic Polyethylene Glycol Shells Cloak Nanoparticles from Uptake by Liver Endothelial Cells for Long Blood Circulation. ACS nano, 12(10), 10130–10141. https://doi.org/10.1021/acsnano.8b04947
534. Cui, Z., Zhang, Y., Xia, K., Yan, Q., Kong, H., Zhang, J., Zuo, X., Shi, J., Wang, L., Zhu, Y., & Fan, C. (2018). Nanodiamond autophagy inhibitor allosterically improves the arsenical-based therapy of solid tumors. Nature communications, 9(1), 4347. https://doi.org/10.1038/s41467-018-06749-2
535. Yakavets, I., Lassalle, H. P., Scheglmann, D., Wiehe, A., Zorin, V., & Bezdetnaya, L. (2018). Temoporfin-in-Cyclodextrin-in-Liposome-A New Approach for Anticancer Drug Delivery: The Optimization of Composition. Nanomaterials (Basel, Switzerland), 8(10), 847. https://doi.org/10.3390/nano8100847
536. Toniolo, G., Efthimiadou, E. K., Kordas, G., & Chatgilialoglu, C. (2018). Development of multi-layered and multi-sensitive polymeric nanocontainers for cancer therapy: in vitro evaluation. Scientific reports, 8(1), 14704. https://doi.org/10.1038/s41598-018-32890-5
537. Jeong, M., Kim, H., Kim, S., & Park, J. H. (2018). Liposomal borrelidin for treatment of metastatic breast cancer. Drug delivery and translational research, 8(5), 1380–1388. https://doi.org/10.1007/s13346-018-0563-z
538. Kong, T., Hao, L., Wei, Y., Cai, X., & Zhu, B. (2018). Doxorubicin conjugated carbon dots as a drug delivery system for human breast cancer therapy. Cell proliferation, 51(5), e12488. https://doi.org/10.1111/cpr.12488
539. Goswami, U., Kandimalla, R., Kalita, S., Chattopadhyay, A., & Ghosh, S. S. (2018). Polyethylene Glycol-Encapsulated Histone Deacetylase Inhibitor Drug-Composite Nanoparticles for Combination Therapy with Artesunate. ACS omega, 3(9), 11504–11516. https://doi.org/10.1021/acsomega.8b02105
540. Meisel, C. L., Bainbridge, P., Mitsouras, D., & Wong, J. Y. (2018). Targeted Nanoparticle Binding to Hydroxyapatite in a High Serum Environment for Early Detection of Heart Disease. ACS applied nano materials, 1(9), 4927–4939. https://doi.org/10.1021/acsanm.8b01099
541. Burkert, S. C., , Shurin, G. V., , White, D. L., , He, X., , Kapralov, A. A., , Kagan, V. E., , Shurin, M. R., , & Star, A., (2018). Targeting myeloid regulators by paclitaxel-loaded enzymatically degradable nanocups. Nanoscale, 10(37), 17990–18000. https://doi.org/10.1039/c8nr04437f
542. Pelivanov, I., Petrova, E., Yoon, S. J., Qian, Z., Guye, K., & O'Donnell, M. (2018). Molecular fingerprinting of nanoparticles in complex media with non-contact photoacoustics: beyond the light scattering limit. Scientific reports, 8(1), 14425. https://doi.org/10.1038/s41598-018-32580-2
543. Wu, Y., Ali, M., Dong, B., Han, T., Chen, K., Chen, J., Tang, Y., Fang, N., Wang, F., & El-Sayed, M. A. (2018). Gold Nanorod Photothermal Therapy Alters Cell Junctions and Actin Network in Inhibiting Cancer Cell Collective Migration. ACS nano, 12(9), 9279–9290. https://doi.org/10.1021/acsnano.8b04128
544. Sunoqrot, S., , Al-Shalabi, E., , & Messersmith, P. B., (2018). Facile synthesis and surface modification of bioinspired nanoparticles from quercetin for drug delivery. Biomaterials science, 6(10), 2656–2666. https://doi.org/10.1039/c8bm00587g
545. Fuchigami, H., Manabe, S., Yasunaga, M., & Matsumura, Y. (2018). Chemotherapy payload of anti-insoluble fibrin antibody-drug conjugate is released specifically upon binding to fibrin. Scientific reports, 8(1), 14211. https://doi.org/10.1038/s41598-018-32601-0
546. Zhang, M., Zhu, J., Zheng, Y., Guo, R., Wang, S., Mignani, S., Caminade, A. M., Majoral, J. P., & Shi, X. (2018). Doxorubicin-Conjugated PAMAM Dendrimers for pH-Responsive Drug Release and Folic Acid-Targeted Cancer Therapy. Pharmaceutics, 10(3), 162. https://doi.org/10.3390/pharmaceutics10030162
547. Shi, N. Q., Li, Y., Zhang, Y., Li, Z. Q., & Qi, X. R. (2018). Deepened cellular/subcellular interface penetration and enhanced antitumor efficacy of cyclic peptidic ligand-decorated accelerating active targeted nanomedicines. International journal of nanomedicine, 13, 5537–5559. https://doi.org/10.2147/IJN.S172556
548. Chen, H., Sha, H., Zhang, L., Qian, H., Chen, F., Ding, N., Ji, L., Zhu, A., Xu, Q., Meng, F., Yu, L., Zhou, Y., & Liu, B. (2018). Lipid insertion enables targeted functionalization of paclitaxel-loaded erythrocyte membrane nanosystem by tumor-penetrating bispecific recombinant protein. International journal of nanomedicine, 13, 5347–5359. https://doi.org/10.2147/IJN.S165109
549. Shankar, G. M., Kirtane, A. R., Miller, J. J., Mazdiyasni, H., Rogner, J., Tai, T., Williams, E. A., Higuchi, F., Juratli, T. A., Tateishi, K., Koerner, M., Tummala, S. S., Fink, A. L., Penson, T., Schmidt, S. P., Wojtkiewicz, G. R., Baig, A., Francis, J. M., Rinne, M. L., Batten, J. M., … Cahill, D. P. (2018). Genotype-targeted local therapy of glioma. Proceedings of the National Academy of Sciences of the United States of America, 115(36), E8388–E8394. https://doi.org/10.1073/pnas.1805751115
550. Vijayan, V., Uthaman, S., & Park, I. K. (2018). Cell Membrane-Camouflaged Nanoparticles: A Promising Biomimetic Strategy for Cancer Theragnostics. Polymers, 10(9), 983. https://doi.org/10.3390/polym10090983
551. Deci, M. B., Liu, M., Dinh, Q. T., & Nguyen, J. (2018). Precision engineering of targeted nanocarriers. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 10(5), e1511. https://doi.org/10.1002/wnan.1511
552. Markwalter, C. E., & Prud'homme, R. K. (2018). Design of a Small-Scale Multi-Inlet Vortex Mixer for Scalable Nanoparticle Production and Application to the Encapsulation of Biologics by Inverse Flash NanoPrecipitation. Journal of pharmaceutical sciences, 107(9), 2465–2471. https://doi.org/10.1016/j.xphs.2018.05.003
553. Deng, H., Dutta, P., & Liu, J. (2018). Stochastic simulations of nanoparticle internalization through transferrin receptor dependent clathrin-mediated endocytosis. Biochimica et biophysica acta. General subjects, 1862(9), 2104–2111. https://doi.org/10.1016/j.bbagen.2018.06.018
554. Wang, S., Yu, G., Wang, Z., Jacobson, O., Tian, R., Lin, L. S., Zhang, F., Wang, J., & Chen, X. (2018). Hierarchical Tumor Microenvironment-Responsive Nanomedicine for Programmed Delivery of Chemotherapeutics. Advanced materials (Deerfield Beach, Fla.), e1803926. Advance online publication. https://doi.org/10.1002/adma.201803926
555. Zhao, J., Wan, Z., Zhou, C., Yang, Q., Dong, J., Song, X., & Gong, T. (2018). Hyaluronic Acid Layer-By-Layer (LbL) Nanoparticles for Synergistic Chemo-Phototherapy. Pharmaceutical research, 35(10), 196. https://doi.org/10.1007/s11095-018-2480-8
556. Stewart, M. P., Langer, R., & Jensen, K. F. (2018). Intracellular Delivery by Membrane Disruption: Mechanisms, Strategies, and Concepts. Chemical reviews, 118(16), 7409–7531. https://doi.org/10.1021/acs.chemrev.7b00678
557. Evangelopoulos, M., Parodi, A., Martinez, J. O., & Tasciotti, E. (2018). Trends towards Biomimicry in Theranostics. Nanomaterials (Basel, Switzerland), 8(9), 637. https://doi.org/10.3390/nano8090637
558. Surapaneni, S. K., Bashir, S., & Tikoo, K. (2018). Gold nanoparticles-induced cytotoxicity in triple negative breast cancer involves different epigenetic alterations depending upon the surface charge. Scientific reports, 8(1), 12295. https://doi.org/10.1038/s41598-018-30541-3
559. Dragulska, S. A., Chen, Y., Wlodarczyk, M. T., Poursharifi, M., Dottino, P., Ulijn, R. V., Martignetti, J. A., & Mieszawska, A. J. (2018). Tripeptide-Stabilized Oil-in-Water Nanoemulsion of an Oleic Acids-Platinum(II) Conjugate as an Anticancer Nanomedicine. Bioconjugate chemistry, 29(8), 2514–2519. https://doi.org/10.1021/acs.bioconjchem.8b00409
560. Ghoreishi, S. M., Khalaj, A., Sabzevari, O., Badrzadeh, L., Mohammadzadeh, P., Mousavi Motlagh, S. S., Bitarafan-Rajabi, A., & Shafiee Ardestani, M. (2018). Technetium-99m chelator-free radiolabeling of specific glutamine tumor imaging nanoprobe: in vitro and in vivo evaluations. International journal of nanomedicine, 13, 4671–4683. https://doi.org/10.2147/IJN.S157426
561. Hsu, H. J., Han, Y., Cheong, M., Král, P., & Hong, S. (2018). Dendritic PEG outer shells enhance serum stability of polymeric micelles. Nanomedicine : nanotechnology, biology, and medicine, 14(6), 1879–1889. https://doi.org/10.1016/j.nano.2018.05.010
562. Heggannavar, G. B., Hiremath, C. G., Achari, D. D., Pangarkar, V. G., & Kariduraganavar, M. Y. (2018). Development of Doxorubicin-Loaded Magnetic Silica-Pluronic F-127 Nanocarriers Conjugated with Transferrin for Treating Glioblastoma across the Blood-Brain Barrier Using an in Vitro Model. ACS omega, 3(7), 8017–8026. https://doi.org/10.1021/acsomega.8b00152
563. Guan, J., Shen, Q., Zhang, Z., Jiang, Z., Yang, Y., Lou, M., Qian, J., Lu, W., & Zhan, C. (2018). Enhanced immunocompatibility of ligand-targeted liposomes by attenuating natural IgM absorption. Nature communications, 9(1), 2982. https://doi.org/10.1038/s41467-018-05384-1
564. Theek, B., Baues, M., Gremse, F., Pola, R., Pechar, M., Negwer, I., Koynov, K., Weber, B., Barz, M., Jahnen-Dechent, W., Storm, G., Kiessling, F., & Lammers, T. (2018). Histidine-rich glycoprotein-induced vascular normalization improves EPR-mediated drug targeting to and into tumors. Journal of controlled release : official journal of the Controlled Release Society, 282, 25–34. https://doi.org/10.1016/j.jconrel.2018.05.002
565. Efremova, M. V., Naumenko, V. A., Spasova, M., Garanina, A. S., Abakumov, M. A., Blokhina, A. D., Melnikov, P. A., Prelovskaya, A. O., Heidelmann, M., Li, Z. A., Ma, Z., Shchetinin, I. V., Golovin, Y. I., Kireev, I. I., Savchenko, A. G., Chekhonin, V. P., Klyachko, N. L., Farle, M., Majouga, A. G., & Wiedwald, U. (2018). Magnetite-Gold nanohybrids as ideal all-in-one platforms for theranostics. Scientific reports, 8(1), 11295. https://doi.org/10.1038/s41598-018-29618-w
566. Wang, P., Fan, Y., Lu, L., Liu, L., Fan, L., Zhao, M., Xie, Y., Xu, C., & Zhang, F. (2018). NIR-II nanoprobes in-vivo assembly to improve image-guided surgery for metastatic ovarian cancer. Nature communications, 9(1), 2898. https://doi.org/10.1038/s41467-018-05113-8
567. Hélix-Nielsen C. (2018). Biomimetic Membranes as a Technology Platform: Challenges and Opportunities. Membranes, 8(3), 44. https://doi.org/10.3390/membranes8030044
568. Guo, F., Wu, J., Wu, W., Huang, D., Yan, Q., Yang, Q., Gao, Y., & Yang, G. (2018). PEGylated self-assembled enzyme-responsive nanoparticles for effective targeted therapy against lung tumors. Journal of nanobiotechnology, 16(1), 57. https://doi.org/10.1186/s12951-018-0384-8
569. Ponzoni, M., Pastorino, F., Di Paolo, D., Perri, P., & Brignole, C. (2018). Targeting Macrophages as a Potential Therapeutic Intervention: Impact on Inflammatory Diseases and Cancer. International journal of molecular sciences, 19(7), 1953. https://doi.org/10.3390/ijms19071953
570. Zhang, T. T., Xu, C. H., Zhao, W., Gu, Y., Li, X. L., Xu, J. J., & Chen, H. Y. (2018). A redox-activated theranostic nanoagent: toward multi-mode imaging guided chemo-photothermal therapy. Chemical science, 9(33), 6749–6757. https://doi.org/10.1039/c8sc02446d
571. Li, F., Wang, Y., Li, D., Chen, Y., Qiao, X., Fardous, R., Lewandowski, A., Liu, J., Chan, T. H., & Dou, Q. P. (2018). Perspectives on the recent developments with green tea polyphenols in drug discovery. Expert opinion on drug discovery, 13(7), 643–660. https://doi.org/10.1080/17460441.2018.1465923
572. Li, L., Hu, S., & Chen, X. (2018). Non-viral delivery systems for CRISPR/Cas9-based genome editing: Challenges and opportunities. Biomaterials, 171, 207–218. https://doi.org/10.1016/j.biomaterials.2018.04.031
573. Nierenberg, D., Khaled, A. R., & Flores, O. (2018). Formation of a protein corona influences the biological identity of nanomaterials. Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology, 23(4), 300–308. https://doi.org/10.1016/j.rpor.2018.05.005
574. Bolu, B. S., Sanyal, R., & Sanyal, A. (2018). Drug Delivery Systems from Self-Assembly of Dendron-Polymer Conjugates †. Molecules (Basel, Switzerland), 23(7), 1570. https://doi.org/10.3390/molecules23071570
575. Waghray, D., & Zhang, Q. (2018). Inhibit or Evade Multidrug Resistance P-Glycoprotein in Cancer Treatment. Journal of medicinal chemistry, 61(12), 5108–5121. https://doi.org/10.1021/acs.jmedchem.7b01457
576. Wu, X., Zhu, Y., Huang, W., Li, J., Zhang, B., Li, Z., & Yang, X. (2018). Hyperbaric Oxygen Potentiates Doxil Antitumor Efficacy by Promoting Tumor Penetration and Sensitizing Cancer Cells. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 5(8), 1700859. https://doi.org/10.1002/advs.201700859
577. Hossen, S., Hossain, M. K., Basher, M. K., Mia, M., Rahman, M. T., & Uddin, M. J. (2018). Smart nanocarrier-based drug delivery systems for cancer therapy and toxicity studies: A review. Journal of advanced research, 15, 1–18. https://doi.org/10.1016/j.jare.2018.06.005
578. Wagner, A. M., Spencer, D. S., & Peppas, N. A. (2018). Advanced architectures in the design of responsive polymers for cancer nanomedicine. Journal of applied polymer science, 135(24), 46154. https://doi.org/10.1002/app.46154
579. Clement, S., Chen, W., Deng, W., & Goldys, E. M. (2018). X-ray radiation-induced and targeted photodynamic therapy with folic acid-conjugated biodegradable nanoconstructs. International journal of nanomedicine, 13, 3553–3570. https://doi.org/10.2147/IJN.S164967
580. Lo Presti, E., Pizzolato, G., Corsale, A. M., Caccamo, N., Sireci, G., Dieli, F., & Meraviglia, S. (2018). γδ T Cells and Tumor Microenvironment: From Immunosurveillance to Tumor Evasion. Frontiers in immunology, 9, 1395. https://doi.org/10.3389/fimmu.2018.01395
581. Li, Y., Wang, Y., Huang, G., & Gao, J. (2018). Cooperativity Principles in Self-Assembled Nanomedicine. Chemical reviews, 118(11), 5359–5391. https://doi.org/10.1021/acs.chemrev.8b00195
582. Pellino, G., Gallo, G., Pallante, P., Capasso, R., De Stefano, A., Maretto, I., Malapelle, U., Qiu, S., Nikolaou, S., Barina, A., Clerico, G., Reginelli, A., Giuliani, A., Sciaudone, G., Kontovounisios, C., Brunese, L., Trompetto, M., & Selvaggi, F. (2018). Noninvasive Biomarkers of Colorectal Cancer: Role in Diagnosis and Personalised Treatment Perspectives. Gastroenterology research and practice, 2018, 2397863. https://doi.org/10.1155/2018/2397863
583. Lu, H. D., Ristroph, K. D., Dobrijevic, E., Feng, J., McManus, S. A., Zhang, Y., Mulhearn, W. D., Ramachandruni, H., Patel, A., & Prud'homme, R. K. (2018). Encapsulation of OZ439 into Nanoparticles for Supersaturated Drug Release in Oral Malaria Therapy. ACS infectious diseases, 4(6), 970–979. https://doi.org/10.1021/acsinfecdis.7b00278
584. Zhang, M., & Merlin, D. (2018). Nanoparticle-Based Oral Drug Delivery Systems Targeting the Colon for Treatment of Ulcerative Colitis. Inflammatory bowel diseases, 24(7), 1401–1415. https://doi.org/10.1093/ibd/izy123
585. Zhu, X., Li, J., Qiu, X., Liu, Y., Feng, W., & Li, F. (2018). Upconversion nanocomposite for programming combination cancer therapy by precise control of microscopic temperature. Nature communications, 9(1), 2176. https://doi.org/10.1038/s41467-018-04571-4
586. Wonder, E., Simón-Gracia, L., Scodeller, P., Majzoub, R. N., Kotamraju, V. R., Ewert, K. K., Teesalu, T., & Safinya, C. R. (2018). Competition of charge-mediated and specific binding by peptide-tagged cationic liposome-DNA nanoparticles in vitro and in vivo. Biomaterials, 166, 52–63. https://doi.org/10.1016/j.biomaterials.2018.02.052
587. Zhong, J. X., Clegg, J. R., Ander, E. W., & Peppas, N. A. (2018). Tunable poly(methacrylic acid-co-acrylamide) nanoparticles through inverse emulsion polymerization. Journal of biomedical materials research. Part A, 106(6), 1677–1686. https://doi.org/10.1002/jbm.a.36371
588. Pereira, R. L., Nascimento, I. C., Santos, A. P., Ogusuku, I., Lameu, C., Mayer, G., & Ulrich, H. (2018). Aptamers: novelty tools for cancer biology. Oncotarget, 9(42), 26934–26953. https://doi.org/10.18632/oncotarget.25260
589. AbouAitah, K., Swiderska-Sroda, A., Farghali, A. A., Wojnarowicz, J., Stefanek, A., Gierlotka, S., Opalinska, A., Allayeh, A. K., Ciach, T., & Lojkowski, W. (2018). Folic acid-conjugated mesoporous silica particles as nanocarriers of natural prodrugs for cancer targeting and antioxidant action. Oncotarget, 9(41), 26466–26490. https://doi.org/10.18632/oncotarget.25470
590. Kim, H., Kim, D., Jeong, J., Jeon, H., & Lee, J. B. (2018). Size-Controllable Enzymatic Synthesis of Short Hairpin RNA Nanoparticles by Controlling the Rate of RNA Polymerization. Polymers, 10(6), 589. https://doi.org/10.3390/polym10060589
591. Wang, H., Agarwal, P., Zhao, G., Ji, G., Jewell, C. M., Fisher, J. P., Lu, X., & He, X. (2018). Overcoming Ovarian Cancer Drug Resistance with a Cold Responsive Nanomaterial. ACS central science, 4(5), 567–581. https://doi.org/10.1021/acscentsci.8b00050
592. Li, E., Yang, Y., Hao, G., Yi, X., Zhang, S., Pan, Y., Xing, B., & Gao, M. (2018). Multifunctional Magnetic Mesoporous Silica Nanoagents for in vivo Enzyme-Responsive Drug Delivery and MR Imaging. Nanotheranostics, 2(3), 233–242. https://doi.org/10.7150/ntno.25565
593. Lai, Y. H., Chiang, C. S., Kao, T. H., & Chen, S. Y. (2018). Dual-drug nanomedicine with hydrophilic F127-modified magnetic nanocarriers assembled in amphiphilic gelatin for enhanced penetration and drug delivery in deep tumor tissue. International journal of nanomedicine, 13, 3011–3026. https://doi.org/10.2147/IJN.S161314
594. Zhou, Q., Zhang, L., Yang, T., & Wu, H. (2018). Stimuli-responsive polymeric micelles for drug delivery and cancer therapy. International journal of nanomedicine, 13, 2921–2942. https://doi.org/10.2147/IJN.S158696
595. Chen, J., Li, X., Zhao, X., Wu, Q., Zhu, H., Mao, Z., & Gao, C. (2018). Doxorubicin-conjugated pH-responsive gold nanorods for combined photothermal therapy and chemotherapy of cancer. Bioactive materials, 3(3), 347–354. https://doi.org/10.1016/j.bioactmat.2018.05.003
596. Merzel, R. L., Orr, B. G., & Banaszak Holl, M. M. (2018). Distributions: The Importance of the Chemist's Molecular View for Biological Materials. Biomacromolecules, 19(5), 1469–1484. https://doi.org/10.1021/acs.biomac.8b00375
597. Li, M., Sun, X., Zhang, N., Wang, W., Yang, Y., Jia, H., & Liu, W. (2018). NIR-Activated Polydopamine-Coated Carrier-Free "Nanobomb" for In Situ On-Demand Drug Release. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 5(7), 1800155. https://doi.org/10.1002/advs.201800155
598. Kimura, N., Maeki, M., Sato, Y., Note, Y., Ishida, A., Tani, H., Harashima, H., & Tokeshi, M. (2018). Development of the iLiNP Device: Fine Tuning the Lipid Nanoparticle Size within 10 nm for Drug Delivery. ACS omega, 3(5), 5044–5051. https://doi.org/10.1021/acsomega.8b00341
599. Fenton, O. S., Olafson, K. N., Pillai, P. S., Mitchell, M. J., & Langer, R. (2018). Advances in Biomaterials for Drug Delivery. Advanced materials (Deerfield Beach, Fla.), e1705328. Advance online publication. https://doi.org/10.1002/adma.201705328
600. Krinsky, N., Kaduri, M., Zinger, A., Shainsky-Roitman, J., Goldfeder, M., Benhar, I., Hershkovitz, D., & Schroeder, A. (2018). Synthetic Cells Synthesize Therapeutic Proteins inside Tumors. Advanced healthcare materials, 7(9), e1701163. https://doi.org/10.1002/adhm.201701163
601. Jin, Y., Jia, J., Li, C., Xue, J., Sun, J., Wang, K., Gan, Y., Xu, J., Shi, Y., & Liang, X. (2018). LAL test and RPT for endotoxin detection of CPT-11/DSPE-mPEG2000 nanoformulation: What if traditional methods are not applicable?. Asian journal of pharmaceutical sciences, 13(3), 289–296. https://doi.org/10.1016/j.ajps.2017.11.003
602. Jin, R., Liu, Z., Bai, Y., Zhou, Y., & Chen, X. (2018). Multiple-Responsive Mesoporous Silica Nanoparticles for Highly Accurate Drugs Delivery to Tumor Cells. ACS omega, 3(4), 4306–4315. https://doi.org/10.1021/acsomega.8b00427
603. Gou, Y., Miao, D., Zhou, M., Wang, L., Zhou, H., & Su, G. (2018). Bio-Inspired Protein-Based Nanoformulations for Cancer Theranostics. Frontiers in pharmacology, 9, 421. https://doi.org/10.3389/fphar.2018.00421
604. McKenzie, M., Ha, S. M., Rammohan, A., Radhakrishnan, R., & Ramakrishnan, N. (2018). Multivalent Binding of a Ligand-Coated Particle: Role of Shape, Size, and Ligand Heterogeneity. Biophysical journal, 114(8), 1830–1846. https://doi.org/10.1016/j.bpj.2018.03.007
605. Jin, M., Jin, G., Kang, L., Chen, L., Gao, Z., & Huang, W. (2018). Smart polymeric nanoparticles with pH-responsive and PEG-detachable properties for co-delivering paclitaxel and survivin siRNA to enhance antitumor outcomes. International journal of nanomedicine, 13, 2405–2426. https://doi.org/10.2147/IJN.S161426
606. Hameed, S., Bhattarai, P., & Dai, Z. (2018). Cerasomes and Bicelles: Hybrid Bilayered Nanostructures With Silica-Like Surface in Cancer Theranostics. Frontiers in chemistry, 6, 127. https://doi.org/10.3389/fchem.2018.00127
607. Yang, H., Guo, J., Tong, R., Yang, C., & Chen, J. K. (2018). pH-Sensitive Micelles Based on Star Copolymer Ad-(PCL-b-PDEAEMA-b-PPEGMA)₄ for Controlled Drug Delivery. Polymers, 10(4), 443. https://doi.org/10.3390/polym10040443
608. Rosenblum, D., Joshi, N., Tao, W., Karp, J. M., & Peer, D. (2018). Progress and challenges towards targeted delivery of cancer therapeutics. Nature communications, 9(1), 1410. https://doi.org/10.1038/s41467-018-03705-y
609. Dan, N., Setua, S., Kashyap, V. K., Khan, S., Jaggi, M., Yallapu, M. M., & Chauhan, S. C. (2018). Antibody-Drug Conjugates for Cancer Therapy: Chemistry to Clinical Implications. Pharmaceuticals (Basel, Switzerland), 11(2), 32. https://doi.org/10.3390/ph11020032
610. Kang, E. S., Kim, D. S., Suhito, I. R., Lee, W., Song, I., & Kim, T. H. (2018). Two-dimensional material-based bionano platforms to control mesenchymal stem cell differentiation. Biomaterials research, 22, 10. https://doi.org/10.1186/s40824-018-0120-3
611. Baudrimont, M., Andrei, J., Mornet, S., Gonzalez, P., Mesmer-Dudons, N., Gourves, P. Y., Jaffal, A., Dedourge-Geffard, O., Geffard, A., Geffard, O., Garric, J., & Feurtet-Mazel, A. (2018). Trophic transfer and effects of gold nanoparticles (AuNPs) in Gammarus fossarum from contaminated periphytic biofilm. Environmental science and pollution research international, 25(12), 11181–11191. https://doi.org/10.1007/s11356-017-8400-3
612. Saratale, R. G., Shin, H. S., Kumar, G., Benelli, G., Ghodake, G. S., Jiang, Y. Y., Kim, D. S., & Saratale, G. D. (2018). Exploiting fruit byproducts for eco-friendly nanosynthesis: Citrus × clementina peel extract mediated fabrication of silver nanoparticles with high efficacy against microbial pathogens and rat glial tumor C6 cells. Environmental science and pollution research international, 25(11), 10250–10263. https://doi.org/10.1007/s11356-017-8724-z
613. Saratale, R. G., Benelli, G., Kumar, G., Kim, D. S., & Saratale, G. D. (2018). Bio-fabrication of silver nanoparticles using the leaf extract of an ancient herbal medicine, dandelion (Taraxacum officinale), evaluation of their antioxidant, anticancer potential, and antimicrobial activity against phytopathogens. Environmental science and pollution research international, 25(11), 10392–10406. https://doi.org/10.1007/s11356-017-9581-5
614. Shamay, Y., Shah, J., Işık, M., Mizrachi, A., Leibold, J., Tschaharganeh, D. F., Roxbury, D., Budhathoki-Uprety, J., Nawaly, K., Sugarman, J. L., Baut, E., Neiman, M. R., Dacek, M., Ganesh, K. S., Johnson, D. C., Sridharan, R., Chu, K. L., Rajasekhar, V. K., Lowe, S. W., Chodera, J. D., … Heller, D. A. (2018). Quantitative self-assembly prediction yields targeted nanomedicines. Nature materials, 17(4), 361–368. https://doi.org/10.1038/s41563-017-0007-z
615. Xue, X., Huang, Y., Wang, X., Wang, Z., Carney, R. P., Li, X., Yuan, Y., He, Y., Lin, T. Y., & Li, Y. (2018). Self-indicating, fully active pharmaceutical ingredients nanoparticles (FAPIN) for multimodal imaging guided trimodality cancer therapy. Biomaterials, 161, 203–215. https://doi.org/10.1016/j.biomaterials.2018.01.044
616. Nedungadi, P., Iyer, A., Gutjahr, G., Bhaskar, J., & Pillai, A. B. (2018). Data-Driven Methods for Advancing Precision Oncology. Current pharmacology reports, 4(2), 145–156. https://doi.org/10.1007/s40495-018-0127-4
617. Tatiparti, K., Sau, S., Gawde, K. A., & Iyer, A. K. (2018). Copper-Free 'Click' Chemistry-Based Synthesis and Characterization of Carbonic Anhydrase-IX Anchored Albumin-Paclitaxel Nanoparticles for Targeting Tumor Hypoxia. International journal of molecular sciences, 19(3), 838. https://doi.org/10.3390/ijms19030838
618. Ribeiro, C., Borges, J., Costa, A., Gaspar, V. M., Bermudez, V. Z., & Mano, J. F. (2018). Preparation of Well-Dispersed Chitosan/Alginate Hollow Multilayered Microcapsules for Enhanced Cellular Internalization. Molecules (Basel, Switzerland), 23(3), 625. https://doi.org/10.3390/molecules23030625
619. Xie, J., Fan, Z., Li, Y., Zhang, Y., Yu, F., Su, G., Xie, L., & Hou, Z. (2018). Design of pH-sensitive methotrexate prodrug-targeted curcumin nanoparticles for efficient dual-drug delivery and combination cancer therapy. International journal of nanomedicine, 13, 1381–1398. https://doi.org/10.2147/IJN.S152312
620. Gholizadeh, S., Dolman, E. M., Wieriks, R., Sparidans, R. W., Hennink, W. E., & Kok, R. J. (2018). Anti-GD2 Immunoliposomes for Targeted Delivery of the Survivin Inhibitor Sepantronium Bromide (YM155) to Neuroblastoma Tumor Cells. Pharmaceutical research, 35(4), 85. https://doi.org/10.1007/s11095-018-2373-x
621. Bai, F., Yin, Y., Chen, T., Chen, J., Ge, M., Lu, Y., Xie, F., Zhang, J., Wu, K., & Liu, Y. (2018). Development of liposomal pemetrexed for enhanced therapy against multidrug resistance mediated by ABCC5 in breast cancer. International journal of nanomedicine, 13, 1327–1339. https://doi.org/10.2147/IJN.S150237
622. Ye, Y., Yu, J., Wen, D., Kahkoska, A. R., & Gu, Z. (2018). Polymeric microneedles for transdermal protein delivery. Advanced drug delivery reviews, 127, 106–118. https://doi.org/10.1016/j.addr.2018.01.015
623. Bayrac, A. T., Akca, O. E., Eyidogan, F. I., & Oktem, H. A. (2018). Target-specific delivery of doxorubicin to human glioblastoma cell line via ssDNA aptamer. Journal of biosciences, 43(1), 97–104.
624. Sarangthem, V., Cho, E. A., Yi, A., Kim, S. K., Lee, B. H., & Park, R. W. (2018). Application of Bld-1-Embedded Elastin-Like Polypeptides in Tumor Targeting. Scientific reports, 8(1), 3892. https://doi.org/10.1038/s41598-018-21910-z
625. Ye, H., Shen, Z., Yu, L., Wei, M., & Li, Y. (2018). Manipulating nanoparticle transport within blood flow through external forces: an exemplar of mechanics in nanomedicine. Proceedings. Mathematical, physical, and engineering sciences, 474(2211), 20170845. https://doi.org/10.1098/rspa.2017.0845
626. Zinger, A., Adir, O., Alper, M., Simon, A., Poley, M., Tzror, C., Yaari, Z., Krayem, M., Kasten, S., Nawy, G., Herman, A., Nir, Y., Akrish, S., Klein, T., Shainsky-Roitman, J., Hershkovitz, D., & Schroeder, A. (2018). Proteolytic Nanoparticles Replace a Surgical Blade by Controllably Remodeling the Oral Connective Tissue. ACS nano, 12(2), 1482–1490. https://doi.org/10.1021/acsnano.7b07983
627. Guimarães, P., Gaglione, S., Sewastianik, T., Carrasco, R. D., Langer, R., & Mitchell, M. J. (2018). Nanoparticles for Immune Cytokine TRAIL-Based Cancer Therapy. ACS nano, 12(2), 912–931. https://doi.org/10.1021/acsnano.7b05876
628. Bachu, R. D., Chowdhury, P., Al-Saedi, Z., Karla, P. K., & Boddu, S. (2018). Ocular Drug Delivery Barriers-Role of Nanocarriers in the Treatment of Anterior Segment Ocular Diseases. Pharmaceutics, 10(1), 28. https://doi.org/10.3390/pharmaceutics10010028
629. Pan, C., Liu, Y., Zhou, M., Wang, W., Shi, M., Xing, M., & Liao, W. (2018). Theranostic pH-sensitive nanoparticles for highly efficient targeted delivery of doxorubicin for breast tumor treatment. International journal of nanomedicine, 13, 1119–1137. https://doi.org/10.2147/IJN.S147464
630. Łukasiewicz, K., & Fol, M. (2018). Microorganisms in the Treatment of Cancer: Advantages and Limitations. Journal of immunology research, 2018, 2397808. https://doi.org/10.1155/2018/2397808
631. Yu, G., Yang, Z., Fu, X., Yung, B. C., Yang, J., Mao, Z., Shao, L., Hua, B., Liu, Y., Zhang, F., Fan, Q., Wang, S., Jacobson, O., Jin, A., Gao, C., Tang, X., Huang, F., & Chen, X. (2018). Polyrotaxane-based supramolecular theranostics. Nature communications, 9(1), 766. https://doi.org/10.1038/s41467-018-03119-w
632. Wang, P., Rahman, M. A., Zhao, Z., Weiss, K., Zhang, C., Chen, Z., Hurwitz, S. J., Chen, Z. G., Shin, D. M., & Ke, Y. (2018). Visualization of the Cellular Uptake and Trafficking of DNA Origami Nanostructures in Cancer Cells. Journal of the American Chemical Society, 140(7), 2478–2484. https://doi.org/10.1021/jacs.7b09024
633. Tsai, H. I., Jiang, L., Zeng, X., Chen, H., Li, Z., Cheng, W., Zhang, J., Pan, J., Wan, D., Gao, L., Xie, Z., Huang, L., Mei, L., & Liu, G. (2018). DACHPt-Loaded Nanoparticles Self-assembled from Biodegradable Dendritic Copolymer Polyglutamic Acid-b-D-α-Tocopheryl Polyethylene Glycol 1000 Succinate for Multidrug Resistant Lung Cancer Therapy. Frontiers in pharmacology, 9, 119. https://doi.org/10.3389/fphar.2018.00119
634. Yang, J., Su, H., Sun, W., Cai, J., Liu, S., Chai, Y., & Zhang, C. (2018). Dual Chemodrug-Loaded Single-Walled Carbon Nanohorns for Multimodal Imaging-Guided Chemo-Photothermal Therapy of Tumors and Lung Metastases. Theranostics, 8(7), 1966–1984. https://doi.org/10.7150/thno.23848
635. Zhang, J., Fang, X., Li, Z., Chan, H. F., Lin, Z., Wang, Y., & Chen, M. (2018). Redox-sensitive micelles composed of disulfide-linked Pluronic-linoleic acid for enhanced anticancer efficiency of brusatol. International journal of nanomedicine, 13, 939–956. https://doi.org/10.2147/IJN.S130696
636. Prusty, D. K., Adam, V., Zadegan, R. M., Irsen, S., & Famulok, M. (2018). Supramolecular aptamer nano-constructs for receptor-mediated targeting and light-triggered release of chemotherapeutics into cancer cells. Nature communications, 9(1), 535. https://doi.org/10.1038/s41467-018-02929-2
637. Wang, H., Li, X., Tse, B. W., Yang, H., Thorling, C. A., Liu, Y., Touraud, M., Chouane, J. B., Liu, X., Roberts, M. S., & Liang, X. (2018). Indocyanine green-incorporating nanoparticles for cancer theranostics. Theranostics, 8(5), 1227–1242. https://doi.org/10.7150/thno.22872
638. Beck, S., Schultze, J., Räder, H. J., Holm, R., Schinnerer, M., Barz, M., Koynov, K., & Zentel, R. (2018). Site-Specific DBCO Modification of DEC205 Antibody for Polymer Conjugation. Polymers, 10(2), 141. https://doi.org/10.3390/polym10020141
639. Myung, J. H., Park, S. J., Wang, A. Z., & Hong, S. (2018). Integration of biomimicry and nanotechnology for significantly improved detection of circulating tumor cells (CTCs). Advanced drug delivery reviews, 125, 36–47. https://doi.org/10.1016/j.addr.2017.12.005
640. Kuhn, P., Eyer, K., & Dittrich, P. S. (2018). A microfluidic device for the delivery of enzymes into cells by liposome fusion. Engineering in life sciences, 18(2), 149–156. https://doi.org/10.1002/elsc.201600150
641. Feng, S., Zhang, H., Zhi, C., Gao, X. D., & Nakanishi, H. (2018). pH-responsive charge-reversal polymer-functionalized boron nitride nanospheres for intracellular doxorubicin delivery. International journal of nanomedicine, 13, 641–652. https://doi.org/10.2147/IJN.S153476
642. Gad, S. F., Park, J., Park, J. E., Fetih, G. N., Tous, S. S., Lee, W., & Yeo, Y. (2018). Enhancing Docetaxel Delivery to Multidrug-Resistant Cancer Cells with Albumin-Coated Nanocrystals. Molecular pharmaceutics, 10.1021/acs.molpharmaceut.7b00783. Advance online publication. https://doi.org/10.1021/acs.molpharmaceut.7b00783
643. Hartshorn, C. M., Bradbury, M. S., Lanza, G. M., Nel, A. E., Rao, J., Wang, A. Z., Wiesner, U. B., Yang, L., & Grodzinski, P. (2018). Nanotechnology Strategies To Advance Outcomes in Clinical Cancer Care. ACS nano, 12(1), 24–43. https://doi.org/10.1021/acsnano.7b05108
644. Mastria, E. M., Cai, L. Y., Kan, M. J., Li, X., Schaal, J. L., Fiering, S., Gunn, M. D., Dewhirst, M. W., Nair, S. K., & Chilkoti, A. (2018). Nanoparticle formulation improves doxorubicin efficacy by enhancing host antitumor immunity. Journal of controlled release : official journal of the Controlled Release Society, 269, 364–373. https://doi.org/10.1016/j.jconrel.2017.11.021
645. Nabar, G. M., Mahajan, K. D., Calhoun, M. A., Duong, A. D., Souva, M. S., Xu, J., Czeisler, C., Puduvalli, V. K., Otero, J. J., Wyslouzil, B. E., & Winter, J. O. (2018). Micelle-templated, poly(lactic-co-glycolic acid) nanoparticles for hydrophobic drug delivery. International journal of nanomedicine, 13, 351–366. https://doi.org/10.2147/IJN.S142079
646. Gadok, A. K., Zhao, C., Meriwether, A. I., Ferrati, S., Rowley, T. G., Zoldan, J., Smyth, H., & Stachowiak, J. C. (2018). The Display of Single-Domain Antibodies on the Surfaces of Connectosomes Enables Gap Junction-Mediated Drug Delivery to Specific Cell Populations. Biochemistry, 57(1), 81–90. https://doi.org/10.1021/acs.biochem.7b00688
647. Jang, S. C., Kang, S. M., Lee, J. Y., Oh, S. Y., Vilian, A. E., Lee, I., Han, Y. K., Park, J. H., Cho, W. S., Roh, C., & Huh, Y. S. (2018). Nano-graphene oxide composite for in vivo imaging. International journal of nanomedicine, 13, 221–234. https://doi.org/10.2147/IJN.S148211
648. Yan, G. H., Wang, K., Shao, Z., Luo, L., Song, Z. M., Chen, J., Jin, R., Deng, X., Wang, H., Cao, Z., Liu, Y., & Cao, A. (2018). Artificial antibody created by conformational reconstruction of the complementary-determining region on gold nanoparticles. Proceedings of the National Academy of Sciences of the United States of America, 115(1), E34–E43. https://doi.org/10.1073/pnas.1713526115
649. Molinaro, R., Corbo, C., Livingston, M., Evangelopoulos, M., Parodi, A., Boada, C., Agostini, M., & Tasciotti, E. (2018). Inflammation and Cancer: In Medio Stat Nano. Current medicinal chemistry, 25(34), 4208–4223. https://doi.org/10.2174/0929867324666170920160030
650. Lin, J., Hu, W., Gao, F., Qin, J., Peng, C., & Lu, X. (2018). Folic acid-modified diatrizoic acid-linked dendrimer-entrapped gold nanoparticles enable targeted CT imaging of human cervical cancer. Journal of Cancer, 9(3), 564–577. https://doi.org/10.7150/jca.19786
651. Li, R., He, Y., Zhang, S., Qin, J., & Wang, J. (2018). Cell membrane-based nanoparticles: a new biomimetic platform for tumor diagnosis and treatment. Acta pharmaceutica Sinica. B, 8(1), 14–22. https://doi.org/10.1016/j.apsb.2017.11.009
652. Palvai, S., Anandi, L., Sarkar, S., Augustus, M., Roy, S., Lahiri, M., & Basu, S. (2017). Drug-Triggered Self-Assembly of Linear Polymer into Nanoparticles for Simultaneous Delivery of Hydrophobic and Hydrophilic Drugs in Breast Cancer Cells. ACS omega, 2(12), 8730–8740. https://doi.org/10.1021/acsomega.7b01400
653. Zhang, B., Hu, Y., & Pang, Z. (2017). Modulating the Tumor Microenvironment to Enhance Tumor Nanomedicine Delivery. Frontiers in pharmacology, 8, 952. https://doi.org/10.3389/fphar.2017.00952
654. Park, W., Cho, S., Han, J., Shin, H., Na, K., Lee, B., & Kim, D. H. (2017). Advanced smart-photosensitizers for more effective cancer treatment. Biomaterials science, 6(1), 79–90. https://doi.org/10.1039/c7bm00872d
655. Niu, W., Teng, I. T., Chen, X., Tan, W., & Veige, A. S. (2017). Aptamer-mediated selective delivery of a cytotoxic cationic NHC-Au(i) complex to cancer cells. Dalton transactions (Cambridge, England : 2003), 47(1), 120–126. https://doi.org/10.1039/c7dt02616a
656. Marofi, F., Vahedi, G., Biglari, A., Esmaeilzadeh, A., & Athari, S. S. (2017). Mesenchymal Stromal/Stem Cells: A New Era in the Cell-Based Targeted Gene Therapy of Cancer. Frontiers in immunology, 8, 1770. https://doi.org/10.3389/fimmu.2017.01770
657. Singh A. K. (2017). Comparative Therapeutic Effects of Plant-Extract Synthesized and Traditionally Synthesized Gold Nanoparticles on Alcohol-Induced Inflammatory Activity in SH-SY5Y Cells In Vitro. Biomedicines, 5(4), 70. https://doi.org/10.3390/biomedicines5040070
658. Guo, S., Li, H., Ma, M., Fu, J., Dong, Y., & Guo, P. (2017). Size, Shape, and Sequence-Dependent Immunogenicity of RNA Nanoparticles. Molecular therapy. Nucleic acids, 9, 399–408. https://doi.org/10.1016/j.omtn.2017.10.010
659. Lian, X., Erazo-Oliveras, A., Pellois, J. P., & Zhou, H. C. (2017). High efficiency and long-term intracellular activity of an enzymatic nanofactory based on metal-organic frameworks. Nature communications, 8(1), 2075. https://doi.org/10.1038/s41467-017-02103-0
660. Rahman, M. A., Wang, P., Zhao, Z., Wang, D., Nannapaneni, S., Zhang, C., Chen, Z., Griffith, C. C., Hurwitz, S. J., Chen, Z. G., Ke, Y., & Shin, D. M. (2017). Systemic Delivery of Bc12-Targeting siRNA by DNA Nanoparticles Suppresses Cancer Cell Growth. Angewandte Chemie (International ed. in English), 56(50), 16023–16027. https://doi.org/10.1002/anie.201709485
661. Jang H. S. (2017). The Diverse Range of Possible Cell Membrane Interactions with Substrates: Drug Delivery, Interfaces and Mobility. Molecules (Basel, Switzerland), 22(12), 2197. https://doi.org/10.3390/molecules22122197
662. Poon, C., Chowdhuri, S., Kuo, C. H., Fang, Y., Alenghat, F. J., Hyatt, D., Kani, K., Gross, M. E., & Chung, E. J. (2017). Protein Mimetic and Anticancer Properties of Monocyte-Targeting Peptide Amphiphile Micelles. ACS biomaterials science & engineering, 3(12), 3273–3282. https://doi.org/10.1021/acsbiomaterials.7b00600
663. Wu, S., Yang, X., Zou, M., Hou, Z., & Yan, J. (2017). A New Method Without Organic Solvent to Targeted Nanodrug for Enhanced Anticancer Efficacy. Nanoscale research letters, 12(1), 416. https://doi.org/10.1186/s11671-017-2174-x
664. Song, W., Musetti, S. N., & Huang, L. (2017). Nanomaterials for cancer immunotherapy. Biomaterials, 148, 16–30. https://doi.org/10.1016/j.biomaterials.2017.09.017
665. Chesson, C. B., & Zloza, A. (2017). Nanoparticles: augmenting tumor antigen presentation for vaccine and immunotherapy treatments of cancer. Nanomedicine (London, England), 12(23), 2693–2706. https://doi.org/10.2217/nnm-2017-0254
666. Ekladious, I., Liu, R., Zhang, H., Foil, D. H., Todd, D. A., Graf, T. N., Padera, R. F., Oberlies, N. H., Colson, Y. L., & Grinstaff, M. W. (2017). Synthesis of poly(1,2-glycerol carbonate)-paclitaxel conjugates and their utility as a single high-dose replacement for multi-dose treatment regimens in peritoneal cancer. Chemical science, 8(12), 8443–8450. https://doi.org/10.1039/c7sc03501b
667. Liu, X. Q., & Tang, R. Z. (2017). Biological responses to nanomaterials: understanding nano-bio effects on cell behaviors. Drug delivery, 24(sup1), 1–15. https://doi.org/10.1080/10717544.2017.1375577
668. Palvai, S., Kuman, M. M., Sengupta, P., & Basu, S. (2017). Hyaluronic Acid Layered Chimeric Nanoparticles: Targeting MAPK-PI3K Signaling Hub in Colon Cancer Cells. ACS omega, 2(11), 7868–7880. https://doi.org/10.1021/acsomega.7b01315
669. Pérez-Medina, C., Hak, S., Reiner, T., Fayad, Z. A., Nahrendorf, M., & Mulder, W. (2017). Integrating nanomedicine and imaging. Philosophical transactions. Series A, Mathematical, physical, and engineering sciences, 375(2107), 20170110. https://doi.org/10.1098/rsta.2017.0110
670. Sun, J., Liu, Y., Ge, M., Zhou, G., Sun, W., Liu, D., Liang, X. J., & Zhang, J. (2017). A Distinct Endocytic Mechanism of Functionalized-Silica Nanoparticles in Breast Cancer Stem Cells. Scientific reports, 7(1), 16236. https://doi.org/10.1038/s41598-017-16591-z
671. Shi, J., Su, Y., Liu, W., Chang, J., & Zhang, Z. (2017). A nanoliposome-based photoactivable drug delivery system for enhanced cancer therapy and overcoming treatment resistance. International journal of nanomedicine, 12, 8257–8275. https://doi.org/10.2147/IJN.S143776
672. Yu, G., Zhang, M., Saha, M. L., Mao, Z., Chen, J., Yao, Y., Zhou, Z., Liu, Y., Gao, C., Huang, F., Chen, X., & Stang, P. J. (2017). Antitumor Activity of a Unique Polymer That Incorporates a Fluorescent Self-Assembled Metallacycle. Journal of the American Chemical Society, 139(44), 15940–15949. https://doi.org/10.1021/jacs.7b09224
673. Naqvi, S., Mohiyuddin, S., & Gopinath, P. (2017). Niclosamide loaded biodegradable chitosan nanocargoes: an in vitro study for potential application in cancer therapy. Royal Society open science, 4(11), 170611. https://doi.org/10.1098/rsos.170611
674. Lee, D. K., Kee, T., Liang, Z., Hsiou, D., Miya, D., Wu, B., Osawa, E., Chow, E. K., Sung, E. C., Kang, M. K., & Ho, D. (2017). Clinical validation of a nanodiamond-embedded thermoplastic biomaterial. Proceedings of the National Academy of Sciences of the United States of America, 114(45), E9445–E9454. https://doi.org/10.1073/pnas.1711924114
675. Fernandes, R. S., de Aguiar Ferreira, C., Soares, D., Maffione, A. M., Townsend, D. M., Rubello, D., & de Barros, A. (2017). The role of radionuclide probes for monitoring anti-tumor drugs efficacy: A brief review. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 95, 469–476. https://doi.org/10.1016/j.biopha.2017.08.079
676. Behzadi, S., Luther, G. A., Harris, M. B., Farokhzad, O. C., & Mahmoudi, M. (2017). Nanomedicine for safe healing of bone trauma: Opportunities and challenges. Biomaterials, 146, 168–182. https://doi.org/10.1016/j.biomaterials.2017.09.005
677. Liang, P., Tang, Q., Cai, Y., Liu, G., Si, W., Shao, J., Huang, W., Zhang, Q., & Dong, X. (2017). Self-quenched ferrocenyl diketopyrrolopyrrole organic nanoparticles with amplifying photothermal effect for cancer therapy. Chemical science, 8(11), 7457–7463. https://doi.org/10.1039/c7sc03351f
678. Xie, J., Li, Y., Song, L., Pan, Z., Ye, S., & Hou, Z. (2017). Design of a novel curcumin-soybean phosphatidylcholine complex-based targeted drug delivery systems. Drug delivery, 24(1), 707–719. https://doi.org/10.1080/10717544.2017.1303855
679. Qu, D., Guo, M., Qin, Y., Wang, L., Zong, B., Chen, Y., & Chen, Y. (2017). A multicomponent microemulsion using rational combination strategy improves lung cancer treatment through synergistic effects and deep tumor penetration. Drug delivery, 24(1), 1179–1190. https://doi.org/10.1080/10717544.2017.1365394
680. Jiang, X., Zhang, B., Zhou, Z., Meng, L., Sun, Z., Xu, Y., Xu, Q., Yuan, A., Yu, L., Qian, H., Wu, J., Hu, Y., & Liu, B. (2017). Enhancement of radiotherapy efficacy by pleiotropic liposomes encapsulated paclitaxel and perfluorotributylamine. Drug delivery, 24(1), 1419–1428. https://doi.org/10.1080/10717544.2017.1378939
681. Yang, X., Li, Z., Wu, Q., Chen, S., Yi, C., & Gong, C. (2017). TRAIL and curcumin codelivery nanoparticles enhance TRAIL-induced apoptosis through upregulation of death receptors. Drug delivery, 24(1), 1526–1536. https://doi.org/10.1080/10717544.2017.1384863
682. Ishak, R., Mostafa, N. M., & Kamel, A. O. (2017). Stealth lipid polymer hybrid nanoparticles loaded with rutin for effective brain delivery - comparative study with the gold standard (Tween 80): optimization, characterization and biodistribution. Drug delivery, 24(1), 1874–1890. https://doi.org/10.1080/10717544.2017.1410263
683. Ju, Z., & Sun, W. (2017). Drug delivery vectors based on filamentous bacteriophages and phage-mimetic nanoparticles. Drug delivery, 24(1), 1898–1908. https://doi.org/10.1080/10717544.2017.1410259
684. Ameruoso, A., Palomba, R., Palange, A. L., Cervadoro, A., Lee, A., Di Mascolo, D., & Decuzzi, P. (2017). Ameliorating Amyloid-β Fibrils Triggered Inflammation via Curcumin-Loaded Polymeric Nanoconstructs. Frontiers in immunology, 8, 1411. https://doi.org/10.3389/fimmu.2017.01411
685. Wu, X., Wang, L., Qiu, Y., Zhang, B., Hu, Z., & Jin, R. (2017). Cooperation of IRAK1/4 inhibitor and ABT-737 in nanoparticles for synergistic therapy of T cell acute lymphoblastic leukemia. International journal of nanomedicine, 12, 8025–8034. https://doi.org/10.2147/IJN.S146875
686. Li, Y., Liu, S., Zhao, X., Wang, Y., Liu, J., Wang, X., & Lu, L. (2017). CO2-based amphiphilic polycarbonate micelles enable a reliable and efficient platform for tumor imaging. Theranostics, 7(19), 4689–4698. https://doi.org/10.7150/thno.21672
687. Mady, F. M., & Shaker, M. A. (2017). Enhanced anticancer activity and oral bioavailability of ellagic acid through encapsulation in biodegradable polymeric nanoparticles. International journal of nanomedicine, 12, 7405–7417. https://doi.org/10.2147/IJN.S147740
688. Yang, F., Fang, X., Jiang, W., & Chen, T. (2017). Bioresponsive cancer-targeted polysaccharide nanosystem to inhibit angiogenesis. International journal of nanomedicine, 12, 7419–7431. https://doi.org/10.2147/IJN.S139405
689. Kim, S. E., Kim, H. J., Rhee, J. K., & Park, K. (2017). Versatile Chemical Derivatizations to Design Glycol Chitosan-Based Drug Carriers. Molecules (Basel, Switzerland), 22(10), 1662. https://doi.org/10.3390/molecules22101662
690. da Silva, A. L., Cruz, F. F., Rocco, P., & Morales, M. M. (2017). New perspectives in nanotherapeutics for chronic respiratory diseases. Biophysical reviews, 9(5), 793–803. https://doi.org/10.1007/s12551-017-0319-x
691. Liu, X., Jiang, J., Ji, Y., Lu, J., Chan, R., & Meng, H. (2017). Targeted drug delivery using iRGD peptide for solid cancer treatment. Molecular systems design & engineering, 2(4), 370–379. https://doi.org/10.1039/C7ME00050B
692. Li, Y., Fu, Y., Ren, Z., Li, X., Mao, C., & Han, G. (2017). Enhanced cell uptake of fluorescent drug-loaded nanoparticles via an implantable photothermal fibrous patch for more effective cancer cell killing. Journal of materials chemistry. B, 5(36), 7504–7511. https://doi.org/10.1039/C7TB01142C
693. Schmidt, S., Tavernaro, I., Cavelius, C., Weber, E., Kümper, A., Schmitz, C., Fleddermann, J., & Kraegeloh, A. (2017). Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein. Nanoscale research letters, 12(1), 545. https://doi.org/10.1186/s11671-017-2280-9
694. Kim, O. Y., Park, H. T., Dinh, N., Choi, S. J., Lee, J., Kim, J. H., Lee, S. W., & Gho, Y. S. (2017). Bacterial outer membrane vesicles suppress tumor by interferon-γ-mediated antitumor response. Nature communications, 8(1), 626. https://doi.org/10.1038/s41467-017-00729-8
695. Cao, Y., Liu, F., Chen, Y., Yu, T., Lou, D., Guo, Y., Li, P., Wang, Z., & Ran, H. (2017). Drug release from core-shell PVA/silk fibroin nanoparticles fabricated by one-step electrospraying. Scientific reports, 7(1), 11913. https://doi.org/10.1038/s41598-017-12351-1
696. Zhou, Z., Kennell, C., Jafari, M., Lee, J. Y., Ruiz-Torres, S. J., Waltz, S. E., & Lee, J. H. (2017). Sequential delivery of erlotinib and doxorubicin for enhanced triple negative Breast cancer treatment using polymeric nanoparticle. International journal of pharmaceutics, 530(1-2), 300–307. https://doi.org/10.1016/j.ijpharm.2017.07.085
697. Luong, D., Kesharwani, P., Alsaab, H. O., Sau, S., Padhye, S., Sarkar, F. H., & Iyer, A. K. (2017). Folic acid conjugated polymeric micelles loaded with a curcumin difluorinated analog for targeting cervical and ovarian cancers. Colloids and surfaces. B, Biointerfaces, 157, 490–502. https://doi.org/10.1016/j.colsurfb.2017.06.025
698. Eyvazzadeh, N., Shakeri-Zadeh, A., Fekrazad, R., Amini, E., Ghaznavi, H., & Kamran Kamrava, S. (2017). Gold-coated magnetic nanoparticle as a nanotheranostic agent for magnetic resonance imaging and photothermal therapy of cancer. Lasers in medical science, 32(7), 1469–1477. https://doi.org/10.1007/s10103-017-2267-x
699. Guo, X., Guo, N., Zhao, J., & Cai, Y. (2017). Active targeting co-delivery system based on hollow mesoporous silica nanoparticles for antitumor therapy in ovarian cancer stem-like cells. Oncology reports, 38(3), 1442–1450. https://doi.org/10.3892/or.2017.5829
700. Bousmail, D., Amrein, L., Fakhoury, J. J., Fakih, H. H., Hsu, J., Panasci, L., & Sleiman, H. F. (2017). Precision spherical nucleic acids for delivery of anticancer drugs. Chemical science, 8(9), 6218–6229. https://doi.org/10.1039/c7sc01619k
701. Amin, D. R., Sugnaux, C., Lau, K., & Messersmith, P. B. (2017). Size Control and Fluorescence Labeling of Polydopamine Melanin-Mimetic Nanoparticles for Intracellular Imaging. Biomimetics (Basel, Switzerland), 2(3), 17. https://doi.org/10.3390/biomimetics2030017
702. Nowacki, M., Peterson, M., Kloskowski, T., McCabe, E., Guiral, D. C., Polom, K., Pietkun, K., Zegarska, B., Pokrywczynska, M., Drewa, T., Roviello, F., Medina, E. A., Habib, S. L., & Zegarski, W. (2017). Nanoparticle as a novel tool in hyperthermic intraperitoneal and pressurized intraperitoneal aerosol chemotheprapy to treat patients with peritoneal carcinomatosis. Oncotarget, 8(44), 78208–78224. https://doi.org/10.18632/oncotarget.20596
703. Kim, M. W., Jeong, H. Y., Kang, S. J., Choi, M. J., You, Y. M., Im, C. S., Lee, T. S., Song, I. H., Lee, C. G., Rhee, K. J., Lee, Y. K., & Park, Y. S. (2017). Cancer-targeted Nucleic Acid Delivery and Quantum Dot Imaging Using EGF Receptor Aptamer-conjugated Lipid Nanoparticles. Scientific reports, 7(1), 9474. https://doi.org/10.1038/s41598-017-09555-w
704. Tawiah, K. D., Porciani, D., & Burke, D. H. (2017). Toward the Selection of Cell Targeting Aptamers with Extended Biological Functionalities to Facilitate Endosomal Escape of Cargoes. Biomedicines, 5(3), 51. https://doi.org/10.3390/biomedicines5030051
705. Wang, W., Wang, P., Tang, X., Elzatahry, A. A., Wang, S., Al-Dahyan, D., Zhao, M., Yao, C., Hung, C. T., Zhu, X., Zhao, T., Li, X., Zhang, F., & Zhao, D. (2017). Facile Synthesis of Uniform Virus-like Mesoporous Silica Nanoparticles for Enhanced Cellular Internalization. ACS central science, 3(8), 839–846. https://doi.org/10.1021/acscentsci.7b00257
706. Lee, A., De Mei, C., Fereira, M., Marotta, R., Yoon, H. Y., Kim, K., Kwon, I. C., & Decuzzi, P. (2017). Dexamethasone-loaded Polymeric Nanoconstructs for Monitoring and Treating Inflammatory Bowel Disease. Theranostics, 7(15), 3653–3666. https://doi.org/10.7150/thno.18183
707. Trenevska, I., Li, D., & Banham, A. H. (2017). Therapeutic Antibodies against Intracellular Tumor Antigens. Frontiers in immunology, 8, 1001. https://doi.org/10.3389/fimmu.2017.01001
708. Ding, B., Wahid, M. A., Wang, Z., Xie, C., Thakkar, A., Prabhu, S., & Wang, J. (2017). Triptolide and celastrol loaded silk fibroin nanoparticles show synergistic effect against human pancreatic cancer cells. Nanoscale, 9(32), 11739–11753. https://doi.org/10.1039/c7nr03016a
709. Caprettini, V., Cerea, A., Melle, G., Lovato, L., Capozza, R., Huang, J. A., Tantussi, F., Dipalo, M., & De Angelis, F. (2017). Soft electroporation for delivering molecules into tightly adherent mammalian cells through 3D hollow nanoelectrodes. Scientific reports, 7(1), 8524. https://doi.org/10.1038/s41598-017-08886-y
710. Chen, G., Wang, Y., Xie, R., & Gong, S. (2017). Tumor-targeted pH/redox dual-sensitive unimolecular nanoparticles for efficient siRNA delivery. Journal of controlled release : official journal of the Controlled Release Society, 259, 105–114. https://doi.org/10.1016/j.jconrel.2017.01.042
711. Xie, S., Manuguri, S., Proietti, G., Romson, J., Fu, Y., Inge, A. K., Wu, B., Zhang, Y., Häll, D., Ramström, O., & Yan, M. (2017). Design and synthesis of theranostic antibiotic nanodrugs that display enhanced antibacterial activity and luminescence. Proceedings of the National Academy of Sciences of the United States of America, 114(32), 8464–8469. https://doi.org/10.1073/pnas.1708556114
712. Yao, C., Rudnitzki, F., Hüttmann, G., Zhang, Z., & Rahmanzadeh, R. (2017). Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation. International journal of nanomedicine, 12, 5659–5672. https://doi.org/10.2147/IJN.S140620
713. Jabeen, N., Maqbool, Q., Sajjad, S., Minhas, A., Younas, U., Anwaar, S., Nazar, M., Kausar, R., & Hussain, S. Z. (2017). Biosynthesis and characterisation of nano-silica as potential system for carrying streptomycin at nano-scale drug delivery. IET nanobiotechnology, 11(5), 557–561. https://doi.org/10.1049/iet-nbt.2016.0106
714. Wei, G., Su, Z., Reynolds, N. P., Arosio, P., Hamley, I. W., Gazit, E., & Mezzenga, R. (2017). Self-assembling peptide and protein amyloids: from structure to tailored function in nanotechnology. Chemical Society reviews, 46(15), 4661–4708. https://doi.org/10.1039/c6cs00542j
715. Singh, V. K., Saini, A., & Chandra, R. (2017). The Implications and Future Perspectives of Nanomedicine for Cancer Stem Cell Targeted Therapies. Frontiers in molecular biosciences, 4, 52. https://doi.org/10.3389/fmolb.2017.00052
716. Ahn, J., Sei, Y. J., Jeon, N. L., & Kim, Y. (2017). Tumor Microenvironment on a Chip: The Progress and Future Perspective. Bioengineering (Basel, Switzerland), 4(3), 64. https://doi.org/10.3390/bioengineering4030064
717. Singh, R., Patil, S., Singh, N., & Gupta, S. (2017). Dual functionality nanobioconjugates targeting intracellular bacteria in cancer cells with enhanced antimicrobial activity. Scientific reports, 7(1), 5792. https://doi.org/10.1038/s41598-017-06014-4
718. Ali, M., Wu, Y., Tang, Y., Xiao, H., Chen, K., Han, T., Fang, N., Wu, R., & El-Sayed, M. A. (2017). Targeting cancer cell integrins using gold nanorods in photothermal therapy inhibits migration through affecting cytoskeletal proteins. Proceedings of the National Academy of Sciences of the United States of America, 114(28), E5655–E5663. https://doi.org/10.1073/pnas.1703151114
719. Li, R., Zheng, K., Yuan, C., Chen, Z., & Huang, M. (2017). Be Active or Not: the Relative Contribution of Active and Passive Tumor Targeting of Nanomaterials. Nanotheranostics, 1(4), 346–357. https://doi.org/10.7150/ntno.19380
720. Palange, A. L., Palomba, R., Rizzuti, I. F., Ferreira, M., & Decuzzi, P. (2017). Deformable Discoidal Polymeric Nanoconstructs for the Precise Delivery of Therapeutic and Imaging Agents. Molecular therapy : the journal of the American Society of Gene Therapy, 25(7), 1514–1521. https://doi.org/10.1016/j.ymthe.2017.02.012
721. Mizrahy, S., Hazan-Halevy, I., Dammes, N., Landesman-Milo, D., & Peer, D. (2017). Current Progress in Non-viral RNAi-Based Delivery Strategies to Lymphocytes. Molecular therapy : the journal of the American Society of Gene Therapy, 25(7), 1491–1500. https://doi.org/10.1016/j.ymthe.2017.03.001
722. Quader, S., & Kataoka, K. (2017). Nanomaterial-Enabled Cancer Therapy. Molecular therapy : the journal of the American Society of Gene Therapy, 25(7), 1501–1513. https://doi.org/10.1016/j.ymthe.2017.04.026
723. Bianco, J., Bastiancich, C., Jankovski, A., des Rieux, A., Préat, V., & Danhier, F. (2017). On glioblastoma and the search for a cure: where do we stand?. Cellular and molecular life sciences : CMLS, 74(13), 2451–2466. https://doi.org/10.1007/s00018-017-2483-3
724. Xue, J., Zhao, Z., Zhang, L., Xue, L., Shen, S., Wen, Y., Wei, Z., Wang, L., Kong, L., Sun, H., Ping, Q., Mo, R., & Zhang, C. (2017). Neutrophil-mediated anticancer drug delivery for suppression of postoperative malignant glioma recurrence. Nature nanotechnology, 12(7), 692–700. https://doi.org/10.1038/nnano.2017.54
725. Yu, Z., Wang, M., Pan, W., Wang, H., Li, N., & Tang, B. (2017). Tumor microenvironment-triggered fabrication of gold nanomachines for tumor-specific photoacoustic imaging and photothermal therapy. Chemical science, 8(7), 4896–4903. https://doi.org/10.1039/c7sc00700k
726. Heo, J. Y., Kang, S. H., Kim, Y. H., You, S., Jin, K. S., Kim, S. W., Jung, H. Y., Jung, K. O., Lee, C. H., Kim, M. J., Sung, S. E., Kim, B., Choi, I. S., Youn, H., Chung, J. K., Kim, S. K., & Kim, Y. (2017). Toward redesigning the PEG surface of nanocarriers for tumor targeting: impact of inner functionalities on size, charge, multivalent binding, and biodistribution. Chemical science, 8(7), 5186–5195. https://doi.org/10.1039/c6sc05640g
727. Mukherjee, S., Dinda, H., Chakraborty, I., Bhattacharyya, R., Das Sarma, J., & Shunmugam, R. (2017). Engineering Camptothecin-Derived Norbornene Polymers for Theranostic Application. ACS omega, 2(6), 2848–2857. https://doi.org/10.1021/acsomega.7b00221
728. Irimie, A. I., Sonea, L., Jurj, A., Mehterov, N., Zimta, A. A., Budisan, L., Braicu, C., & Berindan-Neagoe, I. (2017). Future trends and emerging issues for nanodelivery systems in oral and oropharyngeal cancer. International journal of nanomedicine, 12, 4593–4606. https://doi.org/10.2147/IJN.S133219
729. Zhai, Y., Su, J., Ran, W., Zhang, P., Yin, Q., Zhang, Z., Yu, H., & Li, Y. (2017). Preparation and Application of Cell Membrane-Camouflaged Nanoparticles for Cancer Therapy. Theranostics, 7(10), 2575–2592. https://doi.org/10.7150/thno.20118
730. Tavernaro, I., Cavelius, C., Peuschel, H., & Kraegeloh, A. (2017). Bright fluorescent silica-nanoparticle probes for high-resolution STED and confocal microscopy. Beilstein journal of nanotechnology, 8, 1283–1296. https://doi.org/10.3762/bjnano.8.130
731. Sobhani, Z., Behnam, M. A., Emami, F., Dehghanian, A., & Jamhiri, I. (2017). Photothermal therapy of melanoma tumor using multiwalled carbon nanotubes. International journal of nanomedicine, 12, 4509–4517. https://doi.org/10.2147/IJN.S134661
732. Cui, Y., Song, X., Li, S., He, B., Yuan, L., Dai, W., Zhang, H., Wang, X., Yang, B., & Zhang, Q. (2017). The impact of receptor recycling on the exocytosis of αvβ3 integrin targeted gold nanoparticles. Oncotarget, 8(24), 38618–38630. https://doi.org/10.18632/oncotarget.16955
733. Yan, L., Miller, J., Yuan, M., Liu, J. F., Busch, T. M., Tsourkas, A., & Cheng, Z. (2017). Improved Photodynamic Therapy Efficacy of Protoporphyrin IX-Loaded Polymeric Micelles Using Erlotinib Pretreatment. Biomacromolecules, 18(6), 1836–1844. https://doi.org/10.1021/acs.biomac.7b00274
734. Mozar, F. S., & Chowdhury, E. H. (2017). Surface-Modification of Carbonate Apatite Nanoparticles Enhances Delivery and Cytotoxicity of Gemcitabine and Anastrozole in Breast Cancer Cells. Pharmaceutics, 9(2), 21. https://doi.org/10.3390/pharmaceutics9020021
735. Ganesh, A. N., Logie, J., McLaughlin, C. K., Barthel, B. L., Koch, T. H., Shoichet, B. K., & Shoichet, M. S. (2017). Leveraging Colloidal Aggregation for Drug-Rich Nanoparticle Formulations. Molecular pharmaceutics, 14(6), 1852–1860. https://doi.org/10.1021/acs.molpharmaceut.6b01015
736. Lee, S., Wang, C., Pan, H. C., Shrestha, S., Meyers, C., Ding, C., Shen, J., Chen, E., Lee, M., Soo, C., Ting, K., & James, A. W. (2017). Combining Smoothened Agonist and NEL-Like Protein-1 Enhances Bone Healing. Plastic and reconstructive surgery, 139(6), 1385–1396. https://doi.org/10.1097/PRS.0000000000003367
737. de la Puente, P., & Azab, A. K. (2017). Nanoparticle delivery systems, general approaches, and their implementation in multiple myeloma. European journal of haematology, 98(6), 529–541. https://doi.org/10.1111/ejh.12870
738. Mangal, S., Gao, W., Li, T., & Zhou, Q. T. (2017). Pulmonary delivery of nanoparticle chemotherapy for the treatment of lung cancers: challenges and opportunities. Acta pharmacologica Sinica, 38(6), 782–797. https://doi.org/10.1038/aps.2017.34
739. Zaimy, M. A., Saffarzadeh, N., Mohammadi, A., Pourghadamyari, H., Izadi, P., Sarli, A., Moghaddam, L. K., Paschepari, S. R., Azizi, H., Torkamandi, S., & Tavakkoly-Bazzaz, J. (2017). New methods in the diagnosis of cancer and gene therapy of cancer based on nanoparticles. Cancer gene therapy, 24(6), 233–243. https://doi.org/10.1038/cgt.2017.16
740. Yang, G., Wang, J., Li, D., & Zhou, S. (2017). Polyanhydride micelles with diverse morphologies for shape-regulated cellular internalization and blood circulation. Regenerative biomaterials, 4(3), 149–157. https://doi.org/10.1093/rb/rbw047
741. Gao, F., Zhang, J., Fu, C., Xie, X., Peng, F., You, J., Tang, H., Wang, Z., Li, P., & Chen, J. (2017). iRGD-modified lipid-polymer hybrid nanoparticles loaded with isoliquiritigenin to enhance anti-breast cancer effect and tumor-targeting ability. International journal of nanomedicine, 12, 4147–4162. https://doi.org/10.2147/IJN.S134148
742. Anderson, C. F., & Cui, H. (2017). Protease-Sensitive Nanomaterials for Cancer Therapeutics and Imaging. Industrial & engineering chemistry research, 56(20), 5761–5777. https://doi.org/10.1021/acs.iecr.7b00990
743. Elgqvist J. (2017). Nanoparticles as Theranostic Vehicles in Experimental and Clinical Applications-Focus on Prostate and Breast Cancer. International journal of molecular sciences, 18(5), 1102. https://doi.org/10.3390/ijms18051102
744. Smith, J., Sprenger, K. G., Liao, R., Joseph, A., Nance, E., & Pfaendtner, J. (2017). Determining dominant driving forces affecting controlled protein release from polymeric nanoparticles. Biointerphases, 12(2), 02D412. https://doi.org/10.1116/1.4983154
745. Sun, Q., Ojha, T., Kiessling, F., Lammers, T., & Shi, Y. (2017). Enhancing Tumor Penetration of Nanomedicines. Biomacromolecules, 18(5), 1449–1459. https://doi.org/10.1021/acs.biomac.7b00068
746. Feng, G., Liu, J., Liu, R., Mao, D., Tomczak, N., & Liu, B. (2017). Ultrasmall Conjugated Polymer Nanoparticles with High Specificity for Targeted Cancer Cell Imaging. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 4(9), 1600407. https://doi.org/10.1002/advs.201600407
747. Zhang, C., Ni, D., Liu, Y., Yao, H., Bu, W., & Shi, J. (2017). Magnesium silicide nanoparticles as a deoxygenation agent for cancer starvation therapy. Nature nanotechnology, 12(4), 378–386. https://doi.org/10.1038/nnano.2016.280
748. Liu, X., Lin, P., Perrett, I., Lin, J., Liao, Y. P., Chang, C. H., Jiang, J., Wu, N., Donahue, T., Wainberg, Z., Nel, A. E., & Meng, H. (2017). Tumor-penetrating peptide enhances transcytosis of silicasome-based chemotherapy for pancreatic cancer. The Journal of clinical investigation, 127(5), 2007–2018. https://doi.org/10.1172/JCI92284
749. Ali, M., Wu, Y., Ghosh, D., Do, B. H., Chen, K., Dawson, M. R., Fang, N., Sulchek, T. A., & El-Sayed, M. A. (2017). Nuclear Membrane-Targeted Gold Nanoparticles Inhibit Cancer Cell Migration and Invasion. ACS nano, 11(4), 3716–3726. https://doi.org/10.1021/acsnano.6b08345
750. Pei, X., Luo, F., Zhang, J., Chen, W., Jiang, C., & Liu, J. (2017). Dehydroascorbic Acids-modified Polymer Micelles Target Cancer Cells to Enhance Anti-tumor Efficacy of Paclitaxel. Scientific reports, 7(1), 975. https://doi.org/10.1038/s41598-017-01168-7
751. Mout, R., Ray, M., Lee, Y. W., Scaletti, F., & Rotello, V. M. (2017). In Vivo Delivery of CRISPR/Cas9 for Therapeutic Gene Editing: Progress and Challenges. Bioconjugate chemistry, 28(4), 880–884. https://doi.org/10.1021/acs.bioconjchem.7b00057
752. Abánades Lázaro, I., Haddad, S., Sacca, S., Orellana-Tavra, C., Fairen-Jimenez, D., & Forgan, R. S. (2017). Selective Surface PEGylation of UiO-66 Nanoparticles for Enhanced Stability, Cell Uptake, and pH-Responsive Drug Delivery. Chem, 2(4), 561–578. https://doi.org/10.1016/j.chempr.2017.02.005
753. Wang, F., Lv, P., Gu, Y., Li, L., Ge, X., & Guo, G. (2017). Galectin-1 knockdown improves drug sensitivity of breast cancer by reducing P-glycoprotein expression through inhibiting the Raf-1/AP-1 signaling pathway. Oncotarget, 8(15), 25097–25106. https://doi.org/10.18632/oncotarget.15341
754. Tung, J., Tew, L. S., Hsu, Y. M., & Khung, Y. L. (2017). A novel 4-arm DNA/RNA Nanoconstruct triggering Rapid Apoptosis of Triple Negative Breast Cancer Cells within 24 hours. Scientific reports, 7(1), 793. https://doi.org/10.1038/s41598-017-00912-3
755. Luong, D., Sau, S., Kesharwani, P., & Iyer, A. K. (2017). Polyvalent Folate-Dendrimer-Coated Iron Oxide Theranostic Nanoparticles for Simultaneous Magnetic Resonance Imaging and Precise Cancer Cell Targeting. Biomacromolecules, 18(4), 1197–1209. https://doi.org/10.1021/acs.biomac.6b01885
756. Zhou, Q., Hou, Y., Zhang, L., Wang, J., Qiao, Y., Guo, S., Fan, L., Yang, T., Zhu, L., & Wu, H. (2017). Dual-pH Sensitive Charge-reversal Nanocomplex for Tumor-targeted Drug Delivery with Enhanced Anticancer Activity. Theranostics, 7(7), 1806–1819. https://doi.org/10.7150/thno.18607
757. Feng, Q., Shen, Y., Fu, Y., Muroski, M. E., Zhang, P., Wang, Q., Xu, C., Lesniak, M. S., Li, G., & Cheng, Y. (2017). Self-Assembly of Gold Nanoparticles Shows Microenvironment-Mediated Dynamic Switching and Enhanced Brain Tumor Targeting. Theranostics, 7(7), 1875–1889. https://doi.org/10.7150/thno.18985
758. Atukorale, P. U., Covarrubias, G., Bauer, L., & Karathanasis, E. (2017). Vascular targeting of nanoparticles for molecular imaging of diseased endothelium. Advanced drug delivery reviews, 113, 141–156. https://doi.org/10.1016/j.addr.2016.09.006
759. Wickens, J. M., Alsaab, H. O., Kesharwani, P., Bhise, K., Amin, M., Tekade, R. K., Gupta, U., & Iyer, A. K. (2017). Recent advances in hyaluronic acid-decorated nanocarriers for targeted cancer therapy. Drug discovery today, 22(4), 665–680. https://doi.org/10.1016/j.drudis.2016.12.009
760. Khodabandehlou, K., Masehi-Lano, J. J., Poon, C., Wang, J., & Chung, E. J. (2017). Targeting cell adhesion molecules with nanoparticles using in vivo and flow-based in vitro models of atherosclerosis. Experimental biology and medicine (Maywood, N.J.), 242(8), 799–812. https://doi.org/10.1177/1535370217693116
761. Ray, M., Lee, Y. W., Scaletti, F., Yu, R., & Rotello, V. M. (2017). Intracellular delivery of proteins by nanocarriers. Nanomedicine (London, England), 12(8), 941–952. https://doi.org/10.2217/nnm-2016-0393
762. Qian, E. A., Wixtrom, A. I., Axtell, J. C., Saebi, A., Jung, D., Rehak, P., Han, Y., Moully, E. H., Mosallaei, D., Chow, S., Messina, M. S., Wang, J. Y., Royappa, A. T., Rheingold, A. L., Maynard, H. D., Král, P., & Spokoyny, A. M. (2017). Atomically precise organomimetic cluster nanomolecules assembled via perfluoroaryl-thiol SNAr chemistry. Nature chemistry, 9(4), 333–340. https://doi.org/10.1038/nchem.2686
763. Ljubimova, J. Y., Sun, T., Mashouf, L., Ljubimov, A. V., Israel, L. L., Ljubimov, V. A., Falahatian, V., & Holler, E. (2017). Covalent nano delivery systems for selective imaging and treatment of brain tumors. Advanced drug delivery reviews, 113, 177–200. https://doi.org/10.1016/j.addr.2017.06.002
764. Niazvand, F., Khorsandi, L., Abbaspour, M., Orazizadeh, M., Varaa, N., Maghzi, M., & Ahmadi, K. (2017). Curcumin-loaded poly lactic-co-glycolic acid nanoparticles effects on mono-iodoacetate -induced osteoarthritis in rats. Veterinary research forum : an international quarterly journal, 8(2), 155–161.
765. Ishijima, A., Minamihata, K., Yamaguchi, S., Yamahira, S., Ichikawa, R., Kobayashi, E., Iijima, M., Shibasaki, Y., Azuma, T., Nagamune, T., & Sakuma, I. (2017). Selective intracellular vaporisation of antibody-conjugated phase-change nano-droplets in vitro. Scientific reports, 7, 44077. https://doi.org/10.1038/srep44077
766. Huang, X., Liao, W., Zhang, G., Kang, S., & Zhang, C. Y. (2017). pH-sensitive micelles self-assembled from polymer brush (PAE-g-cholesterol)-b-PEG-b-(PAE-g-cholesterol) for anticancer drug delivery and controlled release. International journal of nanomedicine, 12, 2215–2226. https://doi.org/10.2147/IJN.S130037
767. Mitchell, M. J., Webster, J., Chung, A., Guimarães, P. P., Khan, O. F., & Langer, R. (2017). Polymeric mechanical amplifiers of immune cytokine-mediated apoptosis. Nature communications, 8, 14179. https://doi.org/10.1038/ncomms14179
768. Raliya, R., Saha, D., Chadha, T. S., Raman, B., & Biswas, P. (2017). Non-invasive aerosol delivery and transport of gold nanoparticles to the brain. Scientific reports, 7, 44718. https://doi.org/10.1038/srep44718
769. Zhu, C., Zhang, S., Song, C., Zhang, Y., Ling, Q., Hoffmann, P. R., Li, J., Chen, T., Zheng, W., & Huang, Z. (2017). Selenium nanoparticles decorated with Ulva lactuca polysaccharide potentially attenuate colitis by inhibiting NF-κB mediated hyper inflammation. Journal of nanobiotechnology, 15(1), 20. https://doi.org/10.1186/s12951-017-0252-y
770. Tang, J., Pérez-Medina, C., Zhao, Y., Sadique, A., Mulder, W. J., & Reiner, T. (2017). A Comprehensive Procedure to Evaluate the In Vivo Performance of Cancer Nanomedicines. Journal of visualized experiments : JoVE, (121), 55271. https://doi.org/10.3791/55271
771. Wang, M., Glass, Z. A., & Xu, Q. (2017). Non-viral delivery of genome-editing nucleases for gene therapy. Gene therapy, 24(3), 144–150. https://doi.org/10.1038/gt.2016.72
772. Zhu, L., Staley, C., Kooby, D., El-Rays, B., Mao, H., & Yang, L. (2017). Current status of biomarker and targeted nanoparticle development: The precision oncology approach for pancreatic cancer therapy. Cancer letters, 388, 139–148. https://doi.org/10.1016/j.canlet.2016.11.030
773. Gowda, R., Kardos, G., Sharma, A., Singh, S., & Robertson, G. P. (2017). Nanoparticle-Based Celecoxib and Plumbagin for the Synergistic Treatment of Melanoma. Molecular cancer therapeutics, 16(3), 440–452. https://doi.org/10.1158/1535-7163.MCT-16-0285
774. Ellison, P. A., Chen, F., Goel, S., Barnhart, T. E., Nickles, R. J., DeJesus, O. T., & Cai, W. (2017). Intrinsic and Stable Conjugation of Thiolated Mesoporous Silica Nanoparticles with Radioarsenic. ACS applied materials & interfaces, 9(8), 6772–6781. https://doi.org/10.1021/acsami.6b14049
775. Huang, L., Zhang, Q., Dai, L., Shen, X., Chen, W., & Cai, K. (2017). Phenylboronic acid-modified hollow silica nanoparticles for dual-responsive delivery of doxorubicin for targeted tumor therapy. Regenerative biomaterials, 4(2), 111–124. https://doi.org/10.1093/rb/rbw045
776. Jasinski, D., Haque, F., Binzel, D. W., & Guo, P. (2017). Advancement of the Emerging Field of RNA Nanotechnology. ACS nano, 11(2), 1142–1164. https://doi.org/10.1021/acsnano.6b05737
777. Gao, X., Yu, T., Xu, G., Guo, G., Liu, X., Hu, X., Wang, X., Liu, Y., Mao, Q., You, C., & Zhou, L. (2017). Enhancing the anti-glioma therapy of doxorubicin by honokiol with biodegradable self-assembling micelles through multiple evaluations. Scientific reports, 7, 43501. https://doi.org/10.1038/srep43501
778. Dabrzalska, M., Janaszewska, A., Zablocka, M., Mignani, S., Majoral, J. P., & Klajnert-Maculewicz, B. (2017). Complexing Methylene Blue with Phosphorus Dendrimers to Increase Photodynamic Activity. Molecules (Basel, Switzerland), 22(3), 345. https://doi.org/10.3390/molecules22030345
779. Chen, G., Jaskula-Sztul, R., Esquibel, C. R., Lou, I., Zheng, Q., Dammalapati, A., Harrison, A., Eliceiri, K. W., Tang, W., Chen, H., & Gong, S. (2017). Neuroendocrine Tumor-Targeted Upconversion Nanoparticle-Based Micelles for Simultaneous NIR-Controlled Combination Chemotherapy and Photodynamic Therapy, and Fluorescence Imaging. Advanced functional materials, 27(8), 1604671. https://doi.org/10.1002/adfm.201604671
780. Li, J., Angsantikul, P., Liu, W., Esteban-Fernández de Ávila, B., Thamphiwatana, S., Xu, M., Sandraz, E., Wang, X., Delezuk, J., Gao, W., Zhang, L., & Wang, J. (2017). Micromotors Spontaneously Neutralize Gastric Acid for pH-Responsive Payload Release. Angewandte Chemie (International ed. in English), 56(8), 2156–2161. https://doi.org/10.1002/anie.201611774
781. Mirlekar, B., Gautam, D., & Chattopadhyay, S. (2017). Chromatin Remodeling Protein SMAR1 Is a Critical Regulator of T Helper Cell Differentiation and Inflammatory Diseases. Frontiers in immunology, 8, 72. https://doi.org/10.3389/fimmu.2017.00072
782. Wang, J., MacEwan, S. R., & Chilkoti, A. (2017). Quantitative Mapping of the Spatial Distribution of Nanoparticles in Endo-Lysosomes by Local pH. Nano letters, 17(2), 1226–1232. https://doi.org/10.1021/acs.nanolett.6b05041
783. Mizrahy, S., Hazan-Halevy, I., Landesman-Milo, D., Ng, B. D., & Peer, D. (2017). Advanced Strategies in Immune Modulation of Cancer Using Lipid-Based Nanoparticles. Frontiers in immunology, 8, 69. https://doi.org/10.3389/fimmu.2017.00069
784. Wang, Y., Cheetham, A. G., Angacian, G., Su, H., Xie, L., & Cui, H. (2017). Peptide-drug conjugates as effective prodrug strategies for targeted delivery. Advanced drug delivery reviews, 110-111, 112–126. https://doi.org/10.1016/j.addr.2016.06.015
785. Zhang, H., Ingham, E. S., Gagnon, M. K., Mahakian, L. M., Liu, J., Foiret, J. L., Willmann, J. K., & Ferrara, K. W. (2017). In vitro characterization and in vivo ultrasound molecular imaging of nucleolin-targeted microbubbles. Biomaterials, 118, 63–73. https://doi.org/10.1016/j.biomaterials.2016.11.026
786. Sanna, V., Singh, C. K., Jashari, R., Adhami, V. M., Chamcheu, J. C., Rady, I., Sechi, M., Mukhtar, H., & Siddiqui, I. A. (2017). Targeted nanoparticles encapsulating (-)-epigallocatechin-3-gallate for prostate cancer prevention and therapy. Scientific reports, 7, 41573. https://doi.org/10.1038/srep41573
787. Jain, C. K., Majumder, H. K., & Roychoudhury, S. (2017). Natural Compounds as Anticancer Agents Targeting DNA Topoisomerases. Current genomics, 18(1), 75–92. https://doi.org/10.2174/1389202917666160808125213
788. Liang, P., Shi, H., Zhu, W., Gui, Q., Xu, Y., Meng, J., Guo, X., Gong, Z., & Chen, H. (2017). Silver nanoparticles enhance the sensitivity of temozolomide on human glioma cells. Oncotarget, 8(5), 7533–7539. https://doi.org/10.18632/oncotarget.13503
789. Luciano, M., Erfanzadeh, M., Zhou, F., Zhu, H., Bornhütter, T., Röder, B., Zhu, Q., & Brückner, C. (2017). In vivo photoacoustic tumor tomography using a quinoline-annulated porphyrin as NIR molecular contrast agent. Organic & biomolecular chemistry, 15(4), 972–983. https://doi.org/10.1039/c6ob02640k
790. Dong, X., Chu, D., & Wang, Z. (2017). Leukocyte-mediated Delivery of Nanotherapeutics in Inflammatory and Tumor Sites. Theranostics, 7(3), 751–763. https://doi.org/10.7150/thno.18069
791. Zulfiqar, B., Mahroo, A., Nasir, K., Farooq, R. K., Jalal, N., Rashid, M. U., & Asghar, K. (2017). Nanomedicine and cancer immunotherapy: focus on indoleamine 2,3-dioxygenase inhibitors. OncoTargets and therapy, 10, 463–476. https://doi.org/10.2147/OTT.S119362
792. Burns, J. M., Saager, R., Majaron, B., Jia, W., & Anvari, B. (2017). Optical properties of biomimetic probes engineered from erythrocytes. Nanotechnology, 28(3), 035101. https://doi.org/10.1088/1361-6528/28/3/035101
793. Huang, H., & Lovell, J. F. (2017). Advanced Functional Nanomaterials for Theranostics. Advanced functional materials, 27(2), 1603524. https://doi.org/10.1002/adfm.201603524
794. Wang, H., Dai, T., Zhou, S., Huang, X., Li, S., Sun, K., Zhou, G., & Dou, H. (2017). Self-Assembly Assisted Fabrication of Dextran-Based Nanohydrogels with Reduction-Cleavable Junctions for Applications as Efficient Drug Delivery Systems. Scientific reports, 7, 40011. https://doi.org/10.1038/srep40011
795. Wallat, J. D., Czapar, A. E., Wang, C., Wen, A. M., Wek, K. S., Yu, X., Steinmetz, N. F., & Pokorski, J. K. (2017). Optical and Magnetic Resonance Imaging Using Fluorous Colloidal Nanoparticles. Biomacromolecules, 18(1), 103–112. https://doi.org/10.1021/acs.biomac.6b01389
796. Ando, D., & Gopinathan, A. (2017). Cooperative Interactions between Different Classes of Disordered Proteins Play a Functional Role in the Nuclear Pore Complex of Baker's Yeast. PloS one, 12(1), e0169455. https://doi.org/10.1371/journal.pone.0169455
797. Jaskula-Sztul, R., Chen, G., Dammalapati, A., Harrison, A., Tang, W., Gong, S., & Chen, H. (2017). AB3-Loaded and Tumor-Targeted Unimolecular Micelles for Medullary Thyroid Cancer Treatment. Journal of materials chemistry. B, 5(1), 151–159. https://doi.org/10.1039/C6TB02530G
798. Chen, B., Dai, W., He, B., Zhang, H., Wang, X., Wang, Y., & Zhang, Q. (2017). Current Multistage Drug Delivery Systems Based on the Tumor Microenvironment. Theranostics, 7(3), 538–558. https://doi.org/10.7150/thno.16684
799. Jia, Y., Omri, A., Krishnan, L., & McCluskie, M. J. (2017). Potential applications of nanoparticles in cancer immunotherapy. Human vaccines & immunotherapeutics, 13(1), 63–74. https://doi.org/10.1080/21645515.2016.1245251
800. Zhang, J., Zu, Y., Dhanasekara, C. S., Li, J., Wu, D., Fan, Z., & Wang, S. (2017). Detection and treatment of atherosclerosis using nanoparticles. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 9(1), 10.1002/wnan.1412. https://doi.org/10.1002/wnan.1412
801. Xiao, B., Ma, L., & Merlin, D. (2017). Nanoparticle-mediated co-delivery of chemotherapeutic agent and siRNA for combination cancer therapy. Expert opinion on drug delivery, 14(1), 65–73. https://doi.org/10.1080/17425247.2016.1205583
802. Liu, J. P., Wang, T. T., Wang, D. G., Dong, A. J., Li, Y. P., & Yu, H. J. (2017). Smart nanoparticles improve therapy for drug-resistant tumors by overcoming pathophysiological barriers. Acta pharmacologica Sinica, 38(1), 1–8. https://doi.org/10.1038/aps.2016.84
803. Yadavalli, T., & Shukla, D. (2017). Role of metal and metal oxide nanoparticles as diagnostic and therapeutic tools for highly prevalent viral infections. Nanomedicine : nanotechnology, biology, and medicine, 13(1), 219–230. https://doi.org/10.1016/j.nano.2016.08.016
804. Sayes, C. M., Aquino, G. V., & Hickey, A. J. (2017). Nanomaterial Drug Products: Manufacturing and Analytical Perspectives. The AAPS journal, 19(1), 18–25. https://doi.org/10.1208/s12248-016-0008-x
805. Shi, J., Kantoff, P. W., Wooster, R., & Farokhzad, O. C. (2017). Cancer nanomedicine: progress, challenges and opportunities. Nature reviews. Cancer, 17(1), 20–37. https://doi.org/10.1038/nrc.2016.108
806. Arranja, A. G., Pathak, V., Lammers, T., & Shi, Y. (2017). Tumor-targeted nanomedicines for cancer theranostics. Pharmacological research, 115, 87–95. https://doi.org/10.1016/j.phrs.2016.11.014
807. Valderrama, A., Reynoso, R., Gómez, R. W., Marquina, V., & Romero, M. (2017). Interactions of calcium with the external surfaces of fullerenes and endofullerenes doped with radioactive sodium iodide. Journal of molecular modeling, 23(1), 15. https://doi.org/10.1007/s00894-016-3187-6
808. Belz, J., Castilla-Ojo, N., Sridhar, S., & Kumar, R. (2017). Radiosensitizing Silica Nanoparticles Encapsulating Docetaxel for Treatment of Prostate Cancer. Methods in molecular biology (Clifton, N.J.), 1530, 403–409. https://doi.org/10.1007/978-1-4939-6646-2_26
809. Jayasimha S. (2017). Nanotechnology in Urology. Indian journal of urology : IJU : journal of the Urological Society of India, 33(1), 13–18. https://doi.org/10.4103/0970-1591.194780
810. Chitgupi, U., Qin, Y., & Lovell, J. F. (2017). Targeted Nanomaterials for Phototherapy. Nanotheranostics, 1(1), 38–58. https://doi.org/10.7150/ntno.17694
811. Desai, V., & Bhushan, A. (2017). Natural Bioactive Compounds: Alternative Approach to the Treatment of Glioblastoma Multiforme. BioMed research international, 2017, 9363040. https://doi.org/10.1155/2017/9363040
812. Coclite, A., Mollica, H., Ranaldo, S., Pascazio, G., de Tullio, M. D., & Decuzzi, P. (2017). Predicting different adhesive regimens of circulating particles at blood capillary walls. Microfluidics and nanofluidics, 21(11), 168. https://doi.org/10.1007/s10404-017-2003-7
813. Bhaskar, S., & Lim, S. (2017). Engineering protein nanocages as carriers for biomedical applications. NPG Asia materials, 9(4), e371. https://doi.org/10.1038/am.2016.128
814. Song, Y., Li, Y., Xu, Q., & Liu, Z. (2016). Mesoporous silica nanoparticles for stimuli-responsive controlled drug delivery: advances, challenges, and outlook. International journal of nanomedicine, 12, 87–110. https://doi.org/10.2147/IJN.S117495
815. Wang, Q., Huang, J. Y., Li, H. Q., Zhao, A. Z., Wang, Y., Zhang, K. Q., Sun, H. T., & Lai, Y. K. (2016). Recent advances on smart TiO2 nanotube platforms for sustainable drug delivery applications. International journal of nanomedicine, 12, 151–165. https://doi.org/10.2147/IJN.S117498
816. Rampersaud, S., Fang, J., Wei, Z., Fabijanic, K., Silver, S., Jaikaran, T., Ruiz, Y., Houssou, M., Yin, Z., Zheng, S., Hashimoto, A., Hoshino, A., Lyden, D., Mahajan, S., & Matsui, H. (2016). The Effect of Cage Shape on Nanoparticle-Based Drug Carriers: Anticancer Drug Release and Efficacy via Receptor Blockade Using Dextran-Coated Iron Oxide Nanocages. Nano letters, 16(12), 7357–7363. https://doi.org/10.1021/acs.nanolett.6b02577
817. Mehta, N., Lyon, J. G., Patil, K., Mokarram, N., Kim, C., & Bellamkonda, R. V. (2016). Bacterial Carriers for Glioblastoma Therapy. Molecular therapy oncolytics, 4, 1–17. https://doi.org/10.1016/j.omto.2016.12.003
818. Wang, M., Ravindranath, S. R., Rahim, M. K., Botvinick, E. L., & Haun, J. B. (2016). Evolution of Multivalent Nanoparticle Adhesion via Specific Molecular Interactions. Langmuir : the ACS journal of surfaces and colloids, 32(49), 13124–13136. https://doi.org/10.1021/acs.langmuir.6b03014
819. Yang, Y., Wang, A., Wei, Q., Schlesener, C., Haag, R., Li, Q., & Li, J. (2016). Hyperbranched Polyglycerol-Induced Porous Silica Nanoparticles as Drug Carriers for Cancer Therapy In Vitro and In Vivo. ChemistryOpen, 6(1), 158–164. https://doi.org/10.1002/open.201600072
820. Marciello, M., Pellico, J., Fernandez-Barahona, I., Herranz, F., Ruiz-Cabello, J., & Filice, M. (2016). Recent advances in the preparation and application of multifunctional iron oxide and liposome-based nanosystems for multimodal diagnosis and therapy. Interface focus, 6(6), 20160055. https://doi.org/10.1098/rsfs.2016.0055
821. Bygd, H. C., & Bratlie, K. M. (2016). Investigating the Synergistic Effects of Combined Modified Alginates on Macrophage Phenotype. Polymers, 8(12), 422. https://doi.org/10.3390/polym8120422
822. Rudnick-Glick, S., Corem-Salkmon, E., Grinberg, I., & Margel, S. (2016). Targeted drug delivery of near IR fluorescent doxorubicin-conjugated poly(ethylene glycol) bisphosphonate nanoparticles for diagnosis and therapy of primary and metastatic bone cancer in a mouse model. Journal of nanobiotechnology, 14(1), 80. https://doi.org/10.1186/s12951-016-0233-6
823. Laan, A. C., Santini, C., Jennings, L., de Jong, M., Bernsen, M. R., & Denkova, A. G. (2016). Radiolabeling polymeric micelles for in vivo evaluation: a novel, fast, and facile method. EJNMMI research, 6(1), 12. https://doi.org/10.1186/s13550-016-0167-x
824. Zhao, M. X., & Zhu, B. J. (2016). The Research and Applications of Quantum Dots as Nano-Carriers for Targeted Drug Delivery and Cancer Therapy. Nanoscale research letters, 11(1), 207. https://doi.org/10.1186/s11671-016-1394-9
825. Cao, L. B., Zeng, S., & Zhao, W. (2016). Highly Stable PEGylated Poly(lactic-co-glycolic acid) (PLGA) Nanoparticles for the Effective Delivery of Docetaxel in Prostate Cancers. Nanoscale research letters, 11(1), 305. https://doi.org/10.1186/s11671-016-1509-3
826. Santos, J. L., Ren, Y., Vandermark, J., Archang, M. M., Williford, J. M., Liu, H. W., Lee, J., Wang, T. H., & Mao, H. Q. (2016). Continuous Production of Discrete Plasmid DNA-Polycation Nanoparticles Using Flash Nanocomplexation. Small (Weinheim an der Bergstrasse, Germany), 12(45), 6214–6222. https://doi.org/10.1002/smll.201601425
827. Kamaly, N., He, J. C., Ausiello, D. A., & Farokhzad, O. C. (2016). Nanomedicines for renal disease: current status and future applications. Nature reviews. Nephrology, 12(12), 738–753. https://doi.org/10.1038/nrneph.2016.156
828. Khosravian, P., Shafiee Ardestani, M., Khoobi, M., Ostad, S. N., Dorkoosh, F. A., Akbari Javar, H., & Amanlou, M. (2016). Mesoporous silica nanoparticles functionalized with folic acid/methionine for active targeted delivery of docetaxel. OncoTargets and therapy, 9, 7315–7330. https://doi.org/10.2147/OTT.S113815
829. Zhang, X. Y., & Zhang, P. Y. (2016). Mitochondria targeting nano agents in cancer therapeutics. Oncology letters, 12(6), 4887–4890. https://doi.org/10.3892/ol.2016.5302 (Retraction published Oncol Lett. 2020 Nov;20(5):238)
830. Gargioni, E., Schulz, F., Raabe, A., Burdak-Rothkamm, S., Rieckmann, T., & Rothkamm, K. (2016). Targeted nanoparticles for tumour radiotherapy enhancement-the long dawn of a golden era?. Annals of translational medicine, 4(24), 523. https://doi.org/10.21037/atm.2016.12.46
831. Chen, C. C., Liu, L., Ma, F., Wong, C. W., Guo, X. E., Chacko, J. V., Farhoodi, H. P., Zhang, S. X., Zimak, J., Ségaliny, A., Riazifar, M., Pham, V., Digman, M. A., Pone, E. J., & Zhao, W. (2016). Elucidation of Exosome Migration across the Blood-Brain Barrier Model In Vitro. Cellular and molecular bioengineering, 9(4), 509–529. https://doi.org/10.1007/s12195-016-0458-3
832. Li, J., & Mooney, D. J. (2016). Designing hydrogels for controlled drug delivery. Nature reviews. Materials, 1(12), 16071. https://doi.org/10.1038/natrevmats.2016.71
833. Karandish, F., Haldar, M. K., You, S., Brooks, A. E., Brooks, B. D., Guo, B., Choi, Y., & Mallik, S. (2016). Prostate-Specific Membrane Antigen Targeted Polymersomes for Delivering Mocetinostat and Docetaxel to Prostate Cancer Cell Spheroids. ACS omega, 1(5), 952–962. https://doi.org/10.1021/acsomega.6b00126
834. Mukherjee, S., Das Sarma, J., & Shunmugam, R. (2016). pH-Sensitive Nanoaggregates for Site-Specific Drug-Delivery as Well as Cancer Cell Imaging. ACS omega, 1(5), 755–764. https://doi.org/10.1021/acsomega.6b00167
835. Yu, G., Cook, T. R., Li, Y., Yan, X., Wu, D., Shao, L., Shen, J., Tang, G., Huang, F., Chen, X., & Stang, P. J. (2016). Tetraphenylethene-based highly emissive metallacage as a component of theranostic supramolecular nanoparticles. Proceedings of the National Academy of Sciences of the United States of America, 113(48), 13720–13725. https://doi.org/10.1073/pnas.1616836113
836. Jo, M. R., Yu, J., Kim, H. J., Song, J. H., Kim, K. M., Oh, J. M., & Choi, S. J. (2016). Titanium Dioxide Nanoparticle-Biomolecule Interactions Influence Oral Absorption. Nanomaterials (Basel, Switzerland), 6(12), 225. https://doi.org/10.3390/nano6120225
837. Wang, F., Li, C., Cheng, J., & Yuan, Z. (2016). Recent Advances on Inorganic Nanoparticle-Based Cancer Therapeutic Agents. International journal of environmental research and public health, 13(12), 1182. https://doi.org/10.3390/ijerph13121182
838. Xia, H., Li, F., Hu, X., Park, W., Wang, S., Jang, Y., Du, Y., Baik, S., Cho, S., Kang, T., Kim, D. H., Ling, D., Hui, K. M., & Hyeon, T. (2016). pH-Sensitive Pt Nanocluster Assembly Overcomes Cisplatin Resistance and Heterogeneous Stemness of Hepatocellular Carcinoma. ACS central science, 2(11), 802–811. https://doi.org/10.1021/acscentsci.6b00197
839. Edmonds, S., Volpe, A., Shmeeda, H., Parente-Pereira, A. C., Radia, R., Baguña-Torres, J., Szanda, I., Severin, G. W., Livieratos, L., Blower, P. J., Maher, J., Fruhwirth, G. O., Gabizon, A., & T M de Rosales, R. (2016). Exploiting the Metal-Chelating Properties of the Drug Cargo for In Vivo Positron Emission Tomography Imaging of Liposomal Nanomedicines. ACS nano, 10(11), 10294–10307. https://doi.org/10.1021/acsnano.6b05935
840. Shi, Y., Shi, B., Dass, A. V., Lu, Y., Sayyadi, N., Kautto, L., Willows, R. D., Chung, R., Piper, J., Nevalainen, H., Walsh, B., Jin, D., & Packer, N. H. (2016). Stable Upconversion Nanohybrid Particles for Specific Prostate Cancer Cell Immunodetection. Scientific reports, 6, 37533. https://doi.org/10.1038/srep37533
841. Sayour, E. J., De Leon, G., Pham, C., Grippin, A., Kemeny, H., Chua, J., Huang, J., Sampson, J. H., Sanchez-Perez, L., Flores, C., & Mitchell, D. A. (2016). Systemic activation of antigen-presenting cells via RNA-loaded nanoparticles. Oncoimmunology, 6(1), e1256527. https://doi.org/10.1080/2162402X.2016.1256527
842. Karimi, M., Mirshekari, H., Moosavi Basri, S. M., Bahrami, S., Moghoofei, M., & Hamblin, M. R. (2016). Bacteriophages and phage-inspired nanocarriers for targeted delivery of therapeutic cargos. Advanced drug delivery reviews, 106(Pt A), 45–62. https://doi.org/10.1016/j.addr.2016.03.003
843. Thaxton, C. S., Rink, J. S., Naha, P. C., & Cormode, D. P. (2016). Lipoproteins and lipoprotein mimetics for imaging and drug delivery. Advanced drug delivery reviews, 106(Pt A), 116–131. https://doi.org/10.1016/j.addr.2016.04.020
844. Yaari, Z., da Silva, D., Zinger, A., Goldman, E., Kajal, A., Tshuva, R., Barak, E., Dahan, N., Hershkovitz, D., Goldfeder, M., Roitman, J. S., & Schroeder, A. (2016). Theranostic barcoded nanoparticles for personalized cancer medicine. Nature communications, 7, 13325. https://doi.org/10.1038/ncomms13325
845. Poon, C., Duan, X., Chan, C., Han, W., & Lin, W. (2016). Nanoscale Coordination Polymers Codeliver Carboplatin and Gemcitabine for Highly Effective Treatment of Platinum-Resistant Ovarian Cancer. Molecular pharmaceutics, 13(11), 3665–3675. https://doi.org/10.1021/acs.molpharmaceut.6b00466
846. Mi, Y., Wolfram, J., Mu, C., Liu, X., Blanco, E., Shen, H., & Ferrari, M. (2016). Enzyme-responsive multistage vector for drug delivery to tumor tissue. Pharmacological research, 113(Pt A), 92–99. https://doi.org/10.1016/j.phrs.2016.08.024
847. Ye, H., Liu, X., Sun, J., Zhu, S., Zhu, Y., & Chang, S. (2016). Enhanced therapeutic efficacy of LHRHa-targeted brucea javanica oil liposomes for ovarian cancer. BMC cancer, 16(1), 831. https://doi.org/10.1186/s12885-016-2870-4
848. Yu, M., Wu, J., Shi, J., & Farokhzad, O. C. (2016). Nanotechnology for protein delivery: Overview and perspectives. Journal of controlled release : official journal of the Controlled Release Society, 240, 24–37. https://doi.org/10.1016/j.jconrel.2015.10.012
849. Cho, H., Gao, J., & Kwon, G. S. (2016). PEG-b-PLA micelles and PLGA-b-PEG-b-PLGA sol-gels for drug delivery. Journal of controlled release : official journal of the Controlled Release Society, 240, 191–201. https://doi.org/10.1016/j.jconrel.2015.12.015
850. Yao, V. J., D'Angelo, S., Butler, K. S., Theron, C., Smith, T. L., Marchiò, S., Gelovani, J. G., Sidman, R. L., Dobroff, A. S., Brinker, C. J., Bradbury, A., Arap, W., & Pasqualini, R. (2016). Ligand-targeted theranostic nanomedicines against cancer. Journal of controlled release : official journal of the Controlled Release Society, 240, 267–286. https://doi.org/10.1016/j.jconrel.2016.01.002
851. Zhang, R. X., Wong, H. L., Xue, H. Y., Eoh, J. Y., & Wu, X. Y. (2016). Nanomedicine of synergistic drug combinations for cancer therapy - Strategies and perspectives. Journal of controlled release : official journal of the Controlled Release Society, 240, 489–503. https://doi.org/10.1016/j.jconrel.2016.06.012
852. Chen, Q., Long, M., Qiu, L., Zhu, M., Li, Z., Qiao, M., Hu, H., Zhao, X., & Chen, D. (2016). Decoration of pH-sensitive copolymer micelles with tumor-specific peptide for enhanced cellular uptake of doxorubicin. International journal of nanomedicine, 11, 5415–5427. https://doi.org/10.2147/IJN.S111950
853. Refuerzo, J. S., Leonard, F., Bulayeva, N., Gorenstein, D., Chiossi, G., Ontiveros, A., Longo, M., & Godin, B. (2016). Uterus-targeted liposomes for preterm labor management: studies in pregnant mice. Scientific reports, 6, 34710. https://doi.org/10.1038/srep34710
854. Lee, B. R., Ko, H. K., Ryu, J. H., Ahn, K. Y., Lee, Y. H., Oh, S. J., Na, J. H., Kim, T. W., Byun, Y., Kwon, I. C., Kim, K., & Lee, J. (2016). Engineered Human Ferritin Nanoparticles for Direct Delivery of Tumor Antigens to Lymph Node and Cancer Immunotherapy. Scientific reports, 6, 35182. https://doi.org/10.1038/srep35182
855. Jiang, D., England, C. G., & Cai, W. (2016). DNA nanomaterials for preclinical imaging and drug delivery. Journal of controlled release : official journal of the Controlled Release Society, 239, 27–38. https://doi.org/10.1016/j.jconrel.2016.08.013
856. Wang, S., Lin, J., Wang, T., Chen, X., & Huang, P. (2016). Recent Advances in Photoacoustic Imaging for Deep-Tissue Biomedical Applications. Theranostics, 6(13), 2394–2413. https://doi.org/10.7150/thno.16715
857. Hu, D., Mezghrani, O., Zhang, L., Chen, Y., Ke, X., & Ci, T. (2016). GE11 peptide modified and reduction-responsive hyaluronic acid-based nanoparticles induced higher efficacy of doxorubicin for breast carcinoma therapy. International journal of nanomedicine, 11, 5125–5147. https://doi.org/10.2147/IJN.S113469
858. Åberg, C., Varela, J. A., Fitzpatrick, L. W., & Dawson, K. A. (2016). Spatial and Structural Metrics for Living Cells Inspired by Statistical Mechanics. Scientific reports, 6, 34457. https://doi.org/10.1038/srep34457
859. Oh, M., Hu, C., Urfano, S. F., Arostegui, M., & Slowinska, K. (2016). Thermoresponsive Collagen/Cell Penetrating Hybrid Peptide as Nanocarrier in Targeting-Free Cell Selection and Uptake. Analytical chemistry, 88(19), 9654–9661. https://doi.org/10.1021/acs.analchem.6b02438
860. Williams, R. M., Jaimes, E. A., & Heller, D. A. (2016). Nanomedicines for kidney diseases. Kidney international, 90(4), 740–745. https://doi.org/10.1016/j.kint.2016.03.041
861. Kang, H., Gravier, J., Bao, K., Wada, H., Lee, J. H., Baek, Y., El Fakhri, G., Gioux, S., Rubin, B. P., Coll, J. L., & Choi, H. S. (2016). Renal Clearable Organic Nanocarriers for Bioimaging and Drug Delivery. Advanced materials (Deerfield Beach, Fla.), 28(37), 8162–8168. https://doi.org/10.1002/adma.201601101
862. Freudenberg, U., Liang, Y., Kiick, K. L., & Werner, C. (2016). Glycosaminoglycan-Based Biohybrid Hydrogels: A Sweet and Smart Choice for Multifunctional Biomaterials. Advanced materials (Deerfield Beach, Fla.), 28(40), 8861–8891. https://doi.org/10.1002/adma.201601908
863. Carter, K. A., Luo, D., Razi, A., Geng, J., Shao, S., Ortega, J., & Lovell, J. F. (2016). Sphingomyelin Liposomes Containing Porphyrin-phospholipid for Irinotecan Chemophototherapy. Theranostics, 6(13), 2329–2336. https://doi.org/10.7150/thno.15701
864. Chu, B., Zhang, L., Qu, Y., Chen, X., Peng, J., Huang, Y., & Qian, Z. (2016). Synthesis, characterization and drug loading property of Monomethoxy-Poly(ethylene glycol)-Poly(ε-caprolactone)-Poly(D,L-lactide) (MPEG-PCLA) copolymers. Scientific reports, 6, 34069. https://doi.org/10.1038/srep34069
865. Liu, H., Zhao, M., Wang, J., Pang, M., Wu, Z., Zhao, L., Yin, Z., & Hong, Z. (2016). Photodynamic therapy of tumors with pyropheophorbide-a-loaded polyethylene glycol-poly(lactic-co-glycolic acid) nanoparticles. International journal of nanomedicine, 11, 4905–4918. https://doi.org/10.2147/IJN.S112541
866. Kenry, Yeo, J. C., & Lim, C. T. (2016). Emerging flexible and wearable physical sensing platforms for healthcare and biomedical applications. Microsystems & nanoengineering, 2, 16043. https://doi.org/10.1038/micronano.2016.43
867. Xu, L., Qiu, X., Zhang, Y., Cao, K., Zhao, X., Wu, J., Hu, Y., & Guo, H. (2016). Liposome encapsulated perfluorohexane enhances radiotherapy in mice without additional oxygen supply. Journal of translational medicine, 14, 268. https://doi.org/10.1186/s12967-016-1033-3
868. Feng, S., Zhang, H., Yan, T., Huang, D., Zhi, C., Nakanishi, H., & Gao, X. D. (2016). Folate-conjugated boron nitride nanospheres for targeted delivery of anticancer drugs. International journal of nanomedicine, 11, 4573–4582. https://doi.org/10.2147/IJN.S110689
869. Aldea, M., Florian, I. A., Kacso, G., Craciun, L., Boca, S., Soritau, O., & Florian, I. S. (2016). Nanoparticles for Targeting Intratumoral Hypoxia: Exploiting a Potential Weakness of Glioblastoma. Pharmaceutical research, 33(9), 2059–2077. https://doi.org/10.1007/s11095-016-1947-8
870. Yoshii, T., Geng, Y., Peyton, S., Mercurio, A. M., & Rotello, V. M. (2016). Biochemical and biomechanical drivers of cancer cell metastasis, drug response and nanomedicine. Drug discovery today, 21(9), 1489–1494. https://doi.org/10.1016/j.drudis.2016.05.011
871. Wang, S., Huang, P., & Chen, X. (2016). Hierarchical Targeting Strategy for Enhanced Tumor Tissue Accumulation/Retention and Cellular Internalization. Advanced materials (Deerfield Beach, Fla.), 28(34), 7340–7364. https://doi.org/10.1002/adma.201601498
872. Park, J., Kadasala, N. R., Abouelmagd, S. A., Castanares, M. A., Collins, D. S., Wei, A., & Yeo, Y. (2016). Polymer-iron oxide composite nanoparticles for EPR-independent drug delivery. Biomaterials, 101, 285–295. https://doi.org/10.1016/j.biomaterials.2016.06.007
873. Cheheltani, R., Ezzibdeh, R. M., Chhour, P., Pulaparthi, K., Kim, J., Jurcova, M., Hsu, J. C., Blundell, C., Litt, H. I., Ferrari, V. A., Allcock, H. R., Sehgal, C. M., & Cormode, D. P. (2016). Tunable, biodegradable gold nanoparticles as contrast agents for computed tomography and photoacoustic imaging. Biomaterials, 102, 87–97. https://doi.org/10.1016/j.biomaterials.2016.06.015
874. Bouchaala, R., Mercier, L., Andreiuk, B., Mély, Y., Vandamme, T., Anton, N., Goetz, J. G., & Klymchenko, A. S. (2016). Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice. Journal of controlled release : official journal of the Controlled Release Society, 236, 57–67. https://doi.org/10.1016/j.jconrel.2016.06.027
875. Zhu, C., Yang, C., Wang, Y., Lin, G., Yang, Y., Wang, X., Zhu, J., Chen, X., Lu, X., Liu, G., & Xia, H. (2016). CCCCC pentadentate chelates with planar Möbius aromaticity and unique properties. Science advances, 2(8), e1601031. https://doi.org/10.1126/sciadv.1601031
876. Karimi, M., Sahandi Zangabad, P., Ghasemi, A., Amiri, M., Bahrami, M., Malekzad, H., Ghahramanzadeh Asl, H., Mahdieh, Z., Bozorgomid, M., Ghasemi, A., Rahmani Taji Boyuk, M. R., & Hamblin, M. R. (2016). Temperature-Responsive Smart Nanocarriers for Delivery Of Therapeutic Agents: Applications and Recent Advances. ACS applied materials & interfaces, 8(33), 21107–21133. https://doi.org/10.1021/acsami.6b00371
877. Cheng, L., Kamkaew, A., Sun, H., Jiang, D., Valdovinos, H. F., Gong, H., England, C. G., Goel, S., Barnhart, T. E., & Cai, W. (2016). Dual-Modality Positron Emission Tomography/Optical Image-Guided Photodynamic Cancer Therapy with Chlorin e6-Containing Nanomicelles. ACS nano, 10(8), 7721–7730. https://doi.org/10.1021/acsnano.6b03074
878. Li, F., Zheng, C., Xin, J., Chen, F., Ling, H., Sun, L., Webster, T. J., Ming, X., & Liu, J. (2016). Enhanced tumor delivery and antitumor response of doxorubicin-loaded albumin nanoparticles formulated based on a Schiff base. International journal of nanomedicine, 11, 3875–3890. https://doi.org/10.2147/IJN.S108689
879. Donovan, A. J., Kalkowski, J., Szymusiak, M., Wang, C., Smith, S. A., Klie, R. F., Morrissey, J. H., & Liu, Y. (2016). Artificial Dense Granules: A Procoagulant Liposomal Formulation Modeled after Platelet Polyphosphate Storage Pools. Biomacromolecules, 17(8), 2572–2581. https://doi.org/10.1021/acs.biomac.6b00577
880. Jiang, X., Bugno, J., Hu, C., Yang, Y., Herold, T., Qi, J., Chen, P., Gurbuxani, S., Arnovitz, S., Strong, J., Ferchen, K., Ulrich, B., Weng, H., Wang, Y., Huang, H., Li, S., Neilly, M. B., Larson, R. A., Le Beau, M. M., Bohlander, S. K., … Chen, J. (2016). Eradication of Acute Myeloid Leukemia with FLT3 Ligand-Targeted miR-150 Nanoparticles. Cancer research, 76(15), 4470–4480. https://doi.org/10.1158/0008-5472.CAN-15-2949
881. Chen, G., Jaskula-Sztul, R., Harrison, A., Dammalapati, A., Xu, W., Cheng, Y., Chen, H., & Gong, S. (2016). KE108-conjugated unimolecular micelles loaded with a novel HDAC inhibitor thailandepsin-A for targeted neuroendocrine cancer therapy. Biomaterials, 97, 22–33. https://doi.org/10.1016/j.biomaterials.2016.04.029
882. Pan, Z. Z., Wang, H. Y., Zhang, M., Lin, T. T., Zhang, W. Y., Zhao, P. F., Tang, Y. S., Xiong, Y., Zeng, Y. E., & Huang, Y. Z. (2016). Nuclear-targeting TAT-PEG-Asp8-doxorubicin polymeric nanoassembly to overcome drug-resistant colon cancer. Acta pharmacologica Sinica, 37(8), 1110–1120. https://doi.org/10.1038/aps.2016.48
883. Li, F., Zhou, X., Zhou, H., Jia, J., Li, L., Zhai, S., & Yan, B. (2016). Reducing Both Pgp Overexpression and Drug Efflux with Anti-Cancer Gold-Paclitaxel Nanoconjugates. PloS one, 11(7), e0160042. https://doi.org/10.1371/journal.pone.0160042
884. Pearson, R. M., Sen, S., Hsu, H. J., Pasko, M., Gaske, M., Král, P., & Hong, S. (2016). Tuning the Selectivity of Dendron Micelles Through Variations of the Poly(ethylene glycol) Corona. ACS nano, 10(7), 6905–6914. https://doi.org/10.1021/acsnano.6b02708
885. Liu, Y., Xu, Y., Wu, M., Fan, L., He, C., Wan, J. B., Li, P., Chen, M., & Li, H. (2016). Vitamin E succinate-conjugated F68 micelles for mitoxantrone delivery in enhancing anticancer activity. International journal of nanomedicine, 11, 3167–3178. https://doi.org/10.2147/IJN.S103556
886. Saini, P., Ganugula, R., Arora, M., & Kumar, M. N. (2016). The Next Generation Non-competitive Active Polyester Nanosystems for Transferrin Receptor-mediated Peroral Transport Utilizing Gambogic Acid as a Ligand. Scientific reports, 6, 29501. https://doi.org/10.1038/srep29501
887. Majzoub, R. N., Wonder, E., Ewert, K. K., Kotamraju, V. R., Teesalu, T., & Safinya, C. R. (2016). Rab11 and Lysotracker Markers Reveal Correlation between Endosomal Pathways and Transfection Efficiency of Surface-Functionalized Cationic Liposome-DNA Nanoparticles. The journal of physical chemistry. B, 120(26), 6439–6453. https://doi.org/10.1021/acs.jpcb.6b04441
888. Dogra, N., Izadi, H., & Vanderlick, T. K. (2016). Micro-motors: A motile bacteria based system for liposome cargo transport. Scientific reports, 6, 29369. https://doi.org/10.1038/srep29369
889. Lv, Y., Hao, L., Hu, W., Ran, Y., Bai, Y., & Zhang, L. (2016). Novel multifunctional pH-sensitive nanoparticles loaded into microbubbles as drug delivery vehicles for enhanced tumor targeting. Scientific reports, 6, 29321. https://doi.org/10.1038/srep29321
890. Ortega-Guerrero, A., Espinosa-Duran, J. M., & Velasco-Medina, J. (2016). TRPV1 channel as a target for cancer therapy using CNT-based drug delivery systems. European biophysics journal : EBJ, 45(5), 423–433. https://doi.org/10.1007/s00249-016-1111-8
891. Ilekis, J. V., Tsilou, E., Fisher, S., Abrahams, V. M., Soares, M. J., Cross, J. C., Zamudio, S., Illsley, N. P., Myatt, L., Colvis, C., Costantine, M. M., Haas, D. M., Sadovsky, Y., Weiner, C., Rytting, E., & Bidwell, G. (2016). Placental origins of adverse pregnancy outcomes: potential molecular targets: an Executive Workshop Summary of the Eunice Kennedy Shriver National Institute of Child Health and Human Development. American journal of obstetrics and gynecology, 215(1 Suppl), S1–S46. https://doi.org/10.1016/j.ajog.2016.03.001
892. Toro-Córdova, A., Ledezma-Gallegos, F., Mondragon-Fuentes, L., Jurado, R., Medina, L. A., Pérez-Rojas, J. M., & Garcia-Lopez, P. (2016). Determination of Liposomal Cisplatin by High-Performance Liquid Chromatography and Its Application in Pharmacokinetic Studies. Journal of chromatographic science, 54(6), 1016–1021. https://doi.org/10.1093/chromsci/bmw039
893. Zhao, P., Xia, G., Dong, S., Jiang, Z. X., & Chen, M. (2016). An iTEP-salinomycin nanoparticle that specifically and effectively inhibits metastases of 4T1 orthotopic breast tumors. Biomaterials, 93, 1–9. https://doi.org/10.1016/j.biomaterials.2016.03.032
894. Pang, B., Yang, X., & Xia, Y. (2016). Putting gold nanocages to work for optical imaging, controlled release and cancer theranostics. Nanomedicine (London, England), 11(13), 1715–1728. https://doi.org/10.2217/nnm-2016-0109
895. Ramakrishnan, N., Tourdot, R. W., Eckmann, D. M., Ayyaswamy, P. S., Muzykantov, V. R., & Radhakrishnan, R. (2016). Biophysically inspired model for functionalized nanocarrier adhesion to cell surface: roles of protein expression and mechanical factors. Royal Society open science, 3(6), 160260. https://doi.org/10.1098/rsos.160260
896. Ma, Y., Mou, Q., Sun, M., Yu, C., Li, J., Huang, X., Zhu, X., Yan, D., & Shen, J. (2016). Cancer Theranostic Nanoparticles Self-Assembled from Amphiphilic Small Molecules with Equilibrium Shift-Induced Renal Clearance. Theranostics, 6(10), 1703–1716. https://doi.org/10.7150/thno.15647
897. Subiel, A., Ashmore, R., & Schettino, G. (2016). Standards and Methodologies for Characterizing Radiobiological Impact of High-Z Nanoparticles. Theranostics, 6(10), 1651–1671. https://doi.org/10.7150/thno.15019
898. Xing, H., Hwang, K., & Lu, Y. (2016). Recent Developments of Liposomes as Nanocarriers for Theranostic Applications. Theranostics, 6(9), 1336–1352. https://doi.org/10.7150/thno.15464
899. Jo, S. D., Ku, S. H., Won, Y. Y., Kim, S. H., & Kwon, I. C. (2016). Targeted Nanotheranostics for Future Personalized Medicine: Recent Progress in Cancer Therapy. Theranostics, 6(9), 1362–1377. https://doi.org/10.7150/thno.15335
900. Huang, J., Li, Y., Orza, A., Lu, Q., Guo, P., Wang, L., Yang, L., & Mao, H. (2016). Magnetic Nanoparticle Facilitated Drug Delivery for Cancer Therapy with Targeted and Image-Guided Approaches. Advanced functional materials, 26(22), 3818–3836. https://doi.org/10.1002/adfm.201504185
901. Jin, Z., Lv, Y., Cao, H., Yao, J., Zhou, J., He, W., & Yin, L. (2016). Core-shell nanocarriers with high paclitaxel loading for passive and active targeting. Scientific reports, 6, 27559. https://doi.org/10.1038/srep27559
902. Anselmo, A. C., & Mitragotri, S. (2016). Nanoparticles in the clinic. Bioengineering & translational medicine, 1(1), 10–29. https://doi.org/10.1002/btm2.10003
903. Jaskula-Sztul, R., Xu, W., Chen, G., Harrison, A., Dammalapati, A., Nair, R., Cheng, Y., Gong, S., & Chen, H. (2016). Thailandepsin A-loaded and octreotide-functionalized unimolecular micelles for targeted neuroendocrine cancer therapy. Biomaterials, 91, 1–10. https://doi.org/10.1016/j.biomaterials.2016.03.010
904. Yildirim, A., Chattaraj, R., Blum, N. T., Goldscheitter, G. M., & Goodwin, A. P. (2016). Stable Encapsulation of Air in Mesoporous Silica Nanoparticles: Fluorocarbon-Free Nanoscale Ultrasound Contrast Agents. Advanced healthcare materials, 5(11), 1290–1298. https://doi.org/10.1002/adhm.201600030
905. Levy, O., Brennen, W. N., Han, E., Rosen, D. M., Musabeyezu, J., Safaee, H., Ranganath, S., Ngai, J., Heinelt, M., Milton, Y., Wang, H., Bhagchandani, S. H., Joshi, N., Bhowmick, N., Denmeade, S. R., Isaacs, J. T., & Karp, J. M. (2016). A prodrug-doped cellular Trojan Horse for the potential treatment of prostate cancer. Biomaterials, 91, 140–150. https://doi.org/10.1016/j.biomaterials.2016.03.023
906. Bendale, Y., Bendale, V., Natu, R., & Paul, S. (2016). Biosynthesized Platinum Nanoparticles Inhibit the Proliferation of Human Lung-Cancer Cells in vitro and Delay the Growth of a Human Lung-Tumor Xenograft in vivo: -In vitro and in vivo Anticancer Activity of bio-Pt NPs. Journal of pharmacopuncture, 19(2), 114–121. https://doi.org/10.3831/KPI.2016.19.012
907. Lv, L., Liu, C., Chen, C., Yu, X., Chen, G., Shi, Y., Qin, F., Ou, J., Qiu, K., & Li, G. (2016). Quercetin and doxorubicin co-encapsulated biotin receptor-targeting nanoparticles for minimizing drug resistance in breast cancer. Oncotarget, 7(22), 32184–32199. https://doi.org/10.18632/oncotarget.8607
908. Piktel, E., Niemirowicz, K., Wątek, M., Wollny, T., Deptuła, P., & Bucki, R. (2016). Recent insights in nanotechnology-based drugs and formulations designed for effective anti-cancer therapy. Journal of nanobiotechnology, 14(1), 39. https://doi.org/10.1186/s12951-016-0193-x
909. Yang, R., Liu, P., Pan, D., Zhang, P., Bai, Z., Xu, Y., Wang, L., Yan, J., Yan, Y., Liu, X., & Yang, M. (2016). An Investigation on a Novel Anti-tumor Fusion Peptide of FSH33-53-IIKK. Journal of Cancer, 7(8), 1010–1019. https://doi.org/10.7150/jca.14425
910. Zhang, Y., Song, W., Geng, J., Chitgupi, U., Unsal, H., Federizon, J., Rzayev, J., Sukumaran, D. K., Alexandridis, P., & Lovell, J. F. (2016). Therapeutic surfactant-stripped frozen micelles. Nature communications, 7, 11649. https://doi.org/10.1038/ncomms11649
911. Kesner, E. E., Saada-Reich, A., & Lorberboum-Galski, H. (2016). Characteristics of Mitochondrial Transformation into Human Cells. Scientific reports, 6, 26057. https://doi.org/10.1038/srep26057
912. Liang, P. C., Chen, Y. C., Chiang, C. F., Mo, L. R., Wei, S. Y., Hsieh, W. Y., & Lin, W. L. (2016). Doxorubicin-modified magnetic nanoparticles as a drug delivery system for magnetic resonance imaging-monitoring magnet-enhancing tumor chemotherapy. International journal of nanomedicine, 11, 2021–2037. https://doi.org/10.2147/IJN.S94139
913. Kalber, T. L., Ordidge, K. L., Southern, P., Loebinger, M. R., Kyrtatos, P. G., Pankhurst, Q. A., Lythgoe, M. F., & Janes, S. M. (2016). Hyperthermia treatment of tumors by mesenchymal stem cell-delivered superparamagnetic iron oxide nanoparticles. International journal of nanomedicine, 11, 1973–1983. https://doi.org/10.2147/IJN.S94255
914. Morgan, C. E., Wasserman, M. A., & Kibbe, M. R. (2016). Targeted Nanotherapies for the Treatment of Surgical Diseases. Annals of surgery, 263(5), 900–907. https://doi.org/10.1097/SLA.0000000000001605
915. Qian, C., Yu, J., Chen, Y., Hu, Q., Xiao, X., Sun, W., Wang, C., Feng, P., Shen, Q. D., & Gu, Z. (2016). Light-Activated Hypoxia-Responsive Nanocarriers for Enhanced Anticancer Therapy. Advanced materials (Deerfield Beach, Fla.), 28(17), 3313–3320. https://doi.org/10.1002/adma.201505869
916. Pitek, A. S., Jameson, S. A., Veliz, F. A., Shukla, S., & Steinmetz, N. F. (2016). Serum albumin 'camouflage' of plant virus based nanoparticles prevents their antibody recognition and enhances pharmacokinetics. Biomaterials, 89, 89–97. https://doi.org/10.1016/j.biomaterials.2016.02.032
917. Shukla, S., & Steinmetz, N. F. (2016). Emerging nanotechnologies for cancer immunotherapy. Experimental biology and medicine (Maywood, N.J.), 241(10), 1116–1126. https://doi.org/10.1177/1535370216647123
918. Luk, B. T., Fang, R. H., Hu, C. M., Copp, J. A., Thamphiwatana, S., Dehaini, D., Gao, W., Zhang, K., Li, S., & Zhang, L. (2016). Safe and Immunocompatible Nanocarriers Cloaked in RBC Membranes for Drug Delivery to Treat Solid Tumors. Theranostics, 6(7), 1004–1011. https://doi.org/10.7150/thno.14471
919. Song, W., Tang, Z., Zhang, D., Wen, X., Lv, S., Liu, Z., Deng, M., & Chen, X. (2016). Solid Tumor Therapy Using a Cannon and Pawn Combination Strategy. Theranostics, 6(7), 1023–1030. https://doi.org/10.7150/thno.14741
920. Qian, C., Chen, Y., Zhu, S., Yu, J., Zhang, L., Feng, P., Tang, X., Hu, Q., Sun, W., Lu, Y., Xiao, X., Shen, Q. D., & Gu, Z. (2016). ATP-Responsive and Near-Infrared-Emissive Nanocarriers for Anticancer Drug Delivery and Real-Time Imaging. Theranostics, 6(7), 1053–1064. https://doi.org/10.7150/thno.14843
921. Butler, K. S., Durfee, P. N., Theron, C., Ashley, C. E., Carnes, E. C., & Brinker, C. J. (2016). Protocells: Modular Mesoporous Silica Nanoparticle-Supported Lipid Bilayers for Drug Delivery. Small (Weinheim an der Bergstrasse, Germany), 12(16), 2173–2185. https://doi.org/10.1002/smll.201502119
922. Mi, Y., Mu, C., Wolfram, J., Deng, Z., Hu, T. Y., Liu, X., Blanco, E., Shen, H., & Ferrari, M. (2016). A Micro/Nano Composite for Combination Treatment of Melanoma Lung Metastasis. Advanced healthcare materials, 5(8), 936–946. https://doi.org/10.1002/adhm.201500910
923. Xue, X., Xu, J., Wang, P. C., & Liang, X. J. (2016). Subcellular Behaviour Evaluation of Nanopharmaceuticals with Aggregation-Induced Emission Molecules. Journal of materials chemistry. C, 4(14), 2719–2730. https://doi.org/10.1039/C5TC03651H
924. Li, H. J., Du, J. Z., Du, X. J., Xu, C. F., Sun, C. Y., Wang, H. X., Cao, Z. T., Yang, X. Z., Zhu, Y. H., Nie, S., & Wang, J. (2016). Stimuli-responsive clustered nanoparticles for improved tumor penetration and therapeutic efficacy. Proceedings of the National Academy of Sciences of the United States of America, 113(15), 4164–4169. https://doi.org/10.1073/pnas.1522080113
925. Kulkarni, A., Rao, P., Natarajan, S., Goldman, A., Sabbisetti, V. S., Khater, Y., Korimerla, N., Chandrasekar, V., Mashelkar, R. A., & Sengupta, S. (2016). Reporter nanoparticle that monitors its anticancer efficacy in real time. Proceedings of the National Academy of Sciences of the United States of America, 113(15), E2104–E2113. https://doi.org/10.1073/pnas.1603455113
926. Williford, J. M., Archang, M. M., Minn, I., Ren, Y., Wo, M., Vandermark, J., Fisher, P. B., Pomper, M. G., & Mao, H. Q. (2016). Critical Length of PEG Grafts on lPEI/DNA Nanoparticles for Efficient in Vivo Delivery. ACS biomaterials science & engineering, 2(4), 567–578. https://doi.org/10.1021/acsbiomaterials.5b00551
927. Pitek, A. S., Wen, A. M., Shukla, S., & Steinmetz, N. F. (2016). The Protein Corona of Plant Virus Nanoparticles Influences their Dispersion Properties, Cellular Interactions, and In Vivo Fates. Small (Weinheim an der Bergstrasse, Germany), 12(13), 1758–1769. https://doi.org/10.1002/smll.201502458
928. Hu, Y., Gong, X., Zhang, J., Chen, F., Fu, C., Li, P., Zou, L., & Zhao, G. (2016). Activated Charge-Reversal Polymeric Nano-System: The Promising Strategy in Drug Delivery for Cancer Therapy. Polymers, 8(4), 99. https://doi.org/10.3390/polym8040099
929. Myerson, J. W., Anselmo, A. C., Liu, Y., Mitragotri, S., Eckmann, D. M., & Muzykantov, V. R. (2016). Non-affinity factors modulating vascular targeting of nano- and microcarriers. Advanced drug delivery reviews, 99(Pt A), 97–112. https://doi.org/10.1016/j.addr.2015.10.011
930. Swierczewska, M., Han, H. S., Kim, K., Park, J. H., & Lee, S. (2016). Polysaccharide-based nanoparticles for theranostic nanomedicine. Advanced drug delivery reviews, 99(Pt A), 70–84. https://doi.org/10.1016/j.addr.2015.11.015
931. Talekar, M., Trivedi, M., Shah, P., Ouyang, Q., Oka, A., Gandham, S., & Amiji, M. M. (2016). Combination wt-p53 and MicroRNA-125b Transfection in a Genetically Engineered Lung Cancer Model Using Dual CD44/EGFR-targeting Nanoparticles. Molecular therapy : the journal of the American Society of Gene Therapy, 24(4), 759–769. https://doi.org/10.1038/mt.2015.225
932. Xu, R., Zhang, G., Mai, J., Deng, X., Segura-Ibarra, V., Wu, S., Shen, J., Liu, H., Hu, Z., Chen, L., Huang, Y., Koay, E., Huang, Y., Liu, J., Ensor, J. E., Blanco, E., Liu, X., Ferrari, M., & Shen, H. (2016). An injectable nanoparticle generator enhances delivery of cancer therapeutics. Nature biotechnology, 34(4), 414–418. https://doi.org/10.1038/nbt.3506
933. Revia, R. A., & Zhang, M. (2016). Magnetite nanoparticles for cancer diagnosis, treatment, and treatment monitoring: recent advances. Materials today (Kidlington, England), 19(3), 157–168. https://doi.org/10.1016/j.mattod.2015.08.022
934. Liu, R., Yu, T., Shi, Z., & Wang, Z. (2016). The preparation of metal-organic frameworks and their biomedical application. International journal of nanomedicine, 11, 1187–1200. https://doi.org/10.2147/IJN.S100877
935. Wang, S., Huang, P., & Chen, X. (2016). Stimuli-Responsive Programmed Specific Targeting in Nanomedicine. ACS nano, 10(3), 2991–2994. https://doi.org/10.1021/acsnano.6b00870
936. Shen, Z., Nieh, M. P., & Li, Y. (2016). Decorating Nanoparticle Surface for Targeted Drug Delivery: Opportunities and Challenges. Polymers, 8(3), 83. https://doi.org/10.3390/polym8030083
937. Gupta, A., Landis, R. F., & Rotello, V. M. (2016). Nanoparticle-Based Antimicrobials: Surface Functionality is Critical. F1000Research, 5, F1000 Faculty Rev-364. https://doi.org/10.12688/f1000research.7595.1
938. Mac, J. T., Nuñez, V., Burns, J. M., Guerrero, Y. A., Vullev, V. I., & Anvari, B. (2016). Erythrocyte-derived nano-probes functionalized with antibodies for targeted near infrared fluorescence imaging of cancer cells. Biomedical optics express, 7(4), 1311–1322. https://doi.org/10.1364/BOE.7.001311
939. Johnstone, T. C., Suntharalingam, K., & Lippard, S. J. (2016). The Next Generation of Platinum Drugs: Targeted Pt(II) Agents, Nanoparticle Delivery, and Pt(IV) Prodrugs. Chemical reviews, 116(5), 3436–3486. https://doi.org/10.1021/acs.chemrev.5b00597
940. Friberg, S., & Nyström, A. M. (2016). NANOMEDICINE: will it offer possibilities to overcome multiple drug resistance in cancer?. Journal of nanobiotechnology, 14, 17. https://doi.org/10.1186/s12951-016-0172-2
941. Hu, Q., Sun, W., Wang, C., & Gu, Z. (2016). Recent advances of cocktail chemotherapy by combination drug delivery systems. Advanced drug delivery reviews, 98, 19–34. https://doi.org/10.1016/j.addr.2015.10.022
942. Anjomshoa, M., Torkzadeh-Mahani, M., Dashtrazmi, E., & Adeli-Sardou, M. (2016). Sonochemical Synthesis and Characterization of the Copper(II) Nanocomplex: DNA- and BSA-Binding, Cell Imaging, and Cytotoxicity Against the Human Carcinoma Cell Lines. Journal of fluorescence, 26(2), 545–558. https://doi.org/10.1007/s10895-015-1739-2
943. Yin, P. T., Shah, S., Pasquale, N. J., Garbuzenko, O. B., Minko, T., & Lee, K. B. (2016). Stem cell-based gene therapy activated using magnetic hyperthermia to enhance the treatment of cancer. Biomaterials, 81, 46–57. https://doi.org/10.1016/j.biomaterials.2015.11.023
944. Patil-Sen, Y., Sadeghpour, A., Rappolt, M., & Kulkarni, C. V. (2016). Facile Preparation of Internally Self-assembled Lipid Particles Stabilized by Carbon Nanotubes. Journal of visualized experiments : JoVE, (108), 53489. https://doi.org/10.3791/53489
945. Pfirschke, C., Engblom, C., Rickelt, S., Cortez-Retamozo, V., Garris, C., Pucci, F., Yamazaki, T., Poirier-Colame, V., Newton, A., Redouane, Y., Lin, Y. J., Wojtkiewicz, G., Iwamoto, Y., Mino-Kenudson, M., Huynh, T. G., Hynes, R. O., Freeman, G. J., Kroemer, G., Zitvogel, L., Weissleder, R., … Pittet, M. J. (2016). Immunogenic Chemotherapy Sensitizes Tumors to Checkpoint Blockade Therapy. Immunity, 44(2), 343–354. https://doi.org/10.1016/j.immuni.2015.11.024
946. Correa, S., Choi, K. Y., Dreaden, E. C., Renggli, K., Shi, A., Gu, L., Shopsowitz, K. E., Quadir, M. A., Ben-Akiva, E., & Hammond, P. T. (2016). Highly scalable, closed-loop synthesis of drug-loaded, layer-by-layer nanoparticles. Advanced functional materials, 26(7), 991–1003. https://doi.org/10.1002/adfm.201504385
947. Liang, Y., & Kiick, K. L. (2016). Liposome-Cross-Linked Hybrid Hydrogels for Glutathione-Triggered Delivery of Multiple Cargo Molecules. Biomacromolecules, 17(2), 601–614. https://doi.org/10.1021/acs.biomac.5b01541
948. Hou, L., Yang, X., Ren, J., Wang, Y., Zhang, H., Feng, Q., Shi, Y., Shan, X., Yuan, Y., & Zhang, Z. (2016). A novel redox-sensitive system based on single-walled carbon nanotubes for chemo-photothermal therapy and magnetic resonance imaging. International journal of nanomedicine, 11, 607–624. https://doi.org/10.2147/IJN.S98476
949. Xing, H., Zhang, C. L., Ruan, G., Zhang, J., Hwang, K., & Lu, Y. (2016). Multimodal Detection of a Small Molecule Target Using Stimuli-Responsive Liposome Triggered by Aptamer-Enzyme Conjugate. Analytical chemistry, 88(3), 1506–1510. https://doi.org/10.1021/acs.analchem.5b04031
950. Liu, X., Yaszemski, M. J., & Lu, L. (2016). Expansile crosslinked polymersomes for pH sensitive delivery of doxorubicin. Biomaterials science, 4(2), 245–249. https://doi.org/10.1039/c5bm00269a
951. Au, J. L., Yeung, B. Z., Wientjes, M. G., Lu, Z., & Wientjes, M. G. (2016). Delivery of cancer therapeutics to extracellular and intracellular targets: Determinants, barriers, challenges and opportunities. Advanced drug delivery reviews, 97, 280–301. https://doi.org/10.1016/j.addr.2015.12.002
952. Chen, S., Yang, K., Tuguntaev, R. G., Mozhi, A., Zhang, J., Wang, P. C., & Liang, X. J. (2016). Targeting tumor microenvironment with PEG-based amphiphilic nanoparticles to overcome chemoresistance. Nanomedicine : nanotechnology, biology, and medicine, 12(2), 269–286. https://doi.org/10.1016/j.nano.2015.10.020
953. Lim, E. K., & Chung, B. H. (2016). Preparation of pyrenyl-based multifunctional nanocomposites for biomedical applications. Nature protocols, 11(2), 236–251. https://doi.org/10.1038/nprot.2015.135
954. Ma, W., Cheetham, A. G., & Cui, H. (2016). Building Nanostructures with Drugs. Nano today, 11(1), 13–30. https://doi.org/10.1016/j.nantod.2015.11.003
955. Nguyen, T. K., Selvanayagam, R., Ho, K., Chen, R., Kutty, S. K., Rice, S. A., Kumar, N., Barraud, N., Duong, H., & Boyer, C. (2016). Co-delivery of nitric oxide and antibiotic using polymeric nanoparticles. Chemical science, 7(2), 1016–1027. https://doi.org/10.1039/c5sc02769a
956. Perillo, E., Porto, S., Falanga, A., Zappavigna, S., Stiuso, P., Tirino, V., Desiderio, V., Papaccio, G., Galdiero, M., Giordano, A., Galdiero, S., & Caraglia, M. (2016). Liposome armed with herpes virus-derived gH625 peptide to overcome doxorubicin resistance in lung adenocarcinoma cell lines. Oncotarget, 7(4), 4077–4092. https://doi.org/10.18632/oncotarget.6013
957. Hudlikar, M. S., Li, X., Gagarinov, I. A., Kolishetti, N., Wolfert, M. A., & Boons, G. J. (2016). Controlled Multi-functionalization Facilitates Targeted Delivery of Nanoparticles to Cancer Cells. Chemistry (Weinheim an der Bergstrasse, Germany), 22(4), 1415–1423. https://doi.org/10.1002/chem.201503999
958. Gujrati, V., Lee, M., Ko, Y. J., Lee, S., Kim, D., Kim, H., Kang, S., Lee, S., Kim, J., Jeon, H., Kim, S. C., Jun, Y., & Jon, S. (2016). Bioengineered yeast-derived vacuoles with enhanced tissue-penetrating ability for targeted cancer therapy. Proceedings of the National Academy of Sciences of the United States of America, 113(3), 710–715. https://doi.org/10.1073/pnas.1509371113
959. Zhang, X., Li, Y., Chen, Y. E., Chen, J., & Ma, P. X. (2016). Cell-free 3D scaffold with two-stage delivery of miRNA-26a to regenerate critical-sized bone defects. Nature communications, 7, 10376. https://doi.org/10.1038/ncomms10376
960. Wang, C. E., Wei, H., Tan, N., Boydston, A. J., & Pun, S. H. (2016). Sunflower Polymers for Folate-Mediated Drug Delivery. Biomacromolecules, 17(1), 69–75. https://doi.org/10.1021/acs.biomac.5b01176
961. Jones, S. K., Lizzio, V., & Merkel, O. M. (2016). Folate Receptor Targeted Delivery of siRNA and Paclitaxel to Ovarian Cancer Cells via Folate Conjugated Triblock Copolymer to Overcome TLR4 Driven Chemotherapy Resistance. Biomacromolecules, 17(1), 76–87. https://doi.org/10.1021/acs.biomac.5b01189
962. Ho, Y. J., Chang, Y. C., & Yeh, C. K. (2016). Improving Nanoparticle Penetration in Tumors by Vascular Disruption with Acoustic Droplet Vaporization. Theranostics, 6(3), 392–403. https://doi.org/10.7150/thno.13727
963. Jenkins, S. V., Srivatsan, A., Reynolds, K. Y., Gao, F., Zhang, Y., Heyes, C. D., Pandey, R. K., & Chen, J. (2016). Understanding the interactions between porphyrin-containing photosensitizers and polymer-coated nanoparticles in model biological environments. Journal of colloid and interface science, 461, 225–231. https://doi.org/10.1016/j.jcis.2015.09.037
964. Gu, L., & Mooney, D. J. (2016). Biomaterials and emerging anticancer therapeutics: engineering the microenvironment. Nature reviews. Cancer, 16(1), 56–66. https://doi.org/10.1038/nrc.2015.3
965. Yan, L., & Li, X. (2016). Biodegradable Stimuli-Responsive Polymeric Micelles for Treatment of Malignancy. Current pharmaceutical biotechnology, 17(3), 227–236. https://doi.org/10.2174/138920101703160206142821
966. Agrahari, V., Agrahari, V., & Mitra, A. K. (2016). Nanocarrier fabrication and macromolecule drug delivery: challenges and opportunities. Therapeutic delivery, 7(4), 257–278. https://doi.org/10.4155/tde-2015-0012
967. Vieira, D. B., & Gamarra, L. F. (2016). Advances in the use of nanocarriers for cancer diagnosis and treatment. Einstein (Sao Paulo, Brazil), 14(1), 99–103. https://doi.org/10.1590/S1679-45082016RB3475
968. Udofot, O., Affram, K., Smith, T., Tshabe, B., Krishnan, S., Sachdeva, M., & Agyare, E. (2016). Pharmacokinetic, biodistribution and therapeutic efficacy of 5-fluorouracil-loaded pH-sensitive PEGylated liposomal nanoparticles in HCT-116 tumor bearing mouse. Journal of nature and science, 2(1), e171.
969. Luk, B. T., & Zhang, L. (2015). Cell membrane-camouflaged nanoparticles for drug delivery. Journal of controlled release : official journal of the Controlled Release Society, 220(Pt B), 600–607. https://doi.org/10.1016/j.jconrel.2015.07.019
970. Nie, S., Zhang, J., Martinez-Zaguilan, R., Sennoune, S., Hossen, M. N., Lichtenstein, A. H., Cao, J., Meyerrose, G. E., Paone, R., Soontrapa, S., Fan, Z., & Wang, S. (2015). Detection of atherosclerotic lesions and intimal macrophages using CD36-targeted nanovesicles. Journal of controlled release : official journal of the Controlled Release Society, 220(Pt A), 61–70. https://doi.org/10.1016/j.jconrel.2015.10.004
971. Robinson, R., Gerlach, W., & Ghandehari, H. (2015). Comparative effect of gold nanorods and nanocages for prostate tumor hyperthermia. Journal of controlled release : official journal of the Controlled Release Society, 220(Pt A), 245–252. https://doi.org/10.1016/j.jconrel.2015.10.036
972. Luo, D., Carter, K. A., Razi, A., Geng, J., Shao, S., Lin, C., Ortega, J., & Lovell, J. F. (2015). Porphyrin-phospholipid liposomes with tunable leakiness. Journal of controlled release : official journal of the Controlled Release Society, 220(Pt A), 484–494. https://doi.org/10.1016/j.jconrel.2015.11.011
973. Astruc D. (2015). Introduction to Nanomedicine. Molecules (Basel, Switzerland), 21(1), E4. https://doi.org/10.3390/molecules21010004
974. Kim, S. S., Harford, J. B., Pirollo, K. F., & Chang, E. H. (2015). Effective treatment of glioblastoma requires crossing the blood-brain barrier and targeting tumors including cancer stem cells: The promise of nanomedicine. Biochemical and biophysical research communications, 468(3), 485–489. https://doi.org/10.1016/j.bbrc.2015.06.137
975. Grayson P. (2015). Izumo1 and Juno: the evolutionary origins and coevolution of essential sperm-egg binding partners. Royal Society open science, 2(12), 150296. https://doi.org/10.1098/rsos.150296
976. Zhou, M., Zhao, J., Tian, M., Song, S., Zhang, R., Gupta, S., Tan, D., Shen, H., Ferrari, M., & Li, C. (2015). Radio-photothermal therapy mediated by a single compartment nanoplatform depletes tumor initiating cells and reduces lung metastasis in the orthotopic 4T1 breast tumor model. Nanoscale, 7(46), 19438–19447. https://doi.org/10.1039/c5nr04587h
977. Curtis, L. T., Wu, M., Lowengrub, J., Decuzzi, P., & Frieboes, H. B. (2015). Computational Modeling of Tumor Response to Drug Release from Vasculature-Bound Nanoparticles. PloS one, 10(12), e0144888. https://doi.org/10.1371/journal.pone.0144888
978. Du, J., Lane, L. A., & Nie, S. (2015). Stimuli-responsive nanoparticles for targeting the tumor microenvironment. Journal of controlled release : official journal of the Controlled Release Society, 219, 205–214. https://doi.org/10.1016/j.jconrel.2015.08.050
979. Liu, D., & Auguste, D. T. (2015). Cancer targeted therapeutics: From molecules to drug delivery vehicles. Journal of controlled release : official journal of the Controlled Release Society, 219, 632–643. https://doi.org/10.1016/j.jconrel.2015.08.041
980. Su, H., Koo, J. M., & Cui, H. (2015). One-component nanomedicine. Journal of controlled release : official journal of the Controlled Release Society, 219, 383–395. https://doi.org/10.1016/j.jconrel.2015.09.056
981. Alexander, J. F., Kozlovskaya, V., Chen, J., Kuncewicz, T., Kharlampieva, E., & Godin, B. (2015). Cubical Shape Enhances the Interaction of Layer-by-Layer Polymeric Particles with Breast Cancer Cells. Advanced healthcare materials, 4(17), 2657–2666. https://doi.org/10.1002/adhm.201500537
982. Arami, H., Khandhar, A., Liggitt, D., & Krishnan, K. M. (2015). In vivo delivery, pharmacokinetics, biodistribution and toxicity of iron oxide nanoparticles. Chemical Society reviews, 44(23), 8576–8607. https://doi.org/10.1039/c5cs00541h
983. Awuah, S. G., Zheng, Y. R., Bruno, P. M., Hemann, M. T., & Lippard, S. J. (2015). A Pt(IV) Pro-drug Preferentially Targets Indoleamine-2,3-dioxygenase, Providing Enhanced Ovarian Cancer Immuno-Chemotherapy. Journal of the American Chemical Society, 137(47), 14854–14857. https://doi.org/10.1021/jacs.5b10182
984. Lu, Y., Hu, Q., Lin, Y., Pacardo, D. B., Wang, C., Sun, W., Ligler, F. S., Dickey, M. D., & Gu, Z. (2015). Transformable liquid-metal nanomedicine. Nature communications, 6, 10066. https://doi.org/10.1038/ncomms10066
985. Wang, Z., Dabrosin, C., Yin, X., Fuster, M. M., Arreola, A., Rathmell, W. K., Generali, D., Nagaraju, G. P., El-Rayes, B., Ribatti, D., Chen, Y. C., Honoki, K., Fujii, H., Georgakilas, A. G., Nowsheen, S., Amedei, A., Niccolai, E., Amin, A., Ashraf, S. S., Helferich, B., … Jensen, L. D. (2015). Broad targeting of angiogenesis for cancer prevention and therapy. Seminars in cancer biology, 35 Suppl(Suppl), S224–S243. https://doi.org/10.1016/j.semcancer.2015.01.001
986. Wang, H., Agarwal, P., Zhao, S., Xu, R. X., Yu, J., Lu, X., & He, X. (2015). Hyaluronic acid-decorated dual responsive nanoparticles of Pluronic F127, PLGA, and chitosan for targeted co-delivery of doxorubicin and irinotecan to eliminate cancer stem-like cells. Biomaterials, 72, 74–89. https://doi.org/10.1016/j.biomaterials.2015.08.048
987. Dai, T., Li, N., Liu, L., Liu, Q., & Zhang, Y. (2015). AMP-Conjugated Quantum Dots: Low Immunotoxicity Both In Vitro and In Vivo. Nanoscale research letters, 10(1), 434. https://doi.org/10.1186/s11671-015-1100-3
988. Wang, H., Agarwal, P., Zhao, S., Yu, J., Lu, X., & He, X. (2015). A biomimetic hybrid nanoplatform for encapsulation and precisely controlled delivery of theranostic agents. [Corrected]. Nature communications, 6, 10081. https://doi.org/10.1038/ncomms10081
989. Miyamoto, T., Kuribayashi, M., Nagao, S., Shomura, Y., Higuchi, Y., & Hirota, S. (2015). Domain-swapped cytochrome cb562 dimer and its nanocage encapsulating a Zn-SO4 cluster in the internal cavity. Chemical science, 6(12), 7336–7342. https://doi.org/10.1039/c5sc02428e
990. Hu, Q., Sun, W., Qian, C., Wang, C., Bomba, H. N., & Gu, Z. (2015). Anticancer Platelet-Mimicking Nanovehicles. Advanced materials (Deerfield Beach, Fla.), 27(44), 7043–7050. https://doi.org/10.1002/adma.201503323
991. Lukianova-Hleb, E. Y., Kim, Y. S., Aryasomayajula, B., Boulikas, T., Phan, J., Hung, M. C., Torchilin, V. P., O'Neill, B. E., & Lapotko, D. O. (2015). Safety and efficacy of quadrapeutics versus chemoradiation in head and neck carcinoma xenograft model. American journal of cancer research, 5(12), 3534–3547.
992. Liu, S. S., Liu, L. J., Xiao, L. Y., Lu, Q., Zhu, H. S., & Kaplan, D. L. (2015). Design of Silk-Vaterite Microsphere Systems as Drug Carriers with pH-responsive Release Behavior. Journal of materials chemistry. B, 3(42), 8314–8320. https://doi.org/10.1039/C5TB01692D
993. Yokoi, K., Chan, D., Kojic, M., Milosevic, M., Engler, D., Matsunami, R., Tanei, T., Saito, Y., Ferrari, M., & Ziemys, A. (2015). Liposomal doxorubicin extravasation controlled by phenotype-specific transport properties of tumor microenvironment and vascular barrier. Journal of controlled release : official journal of the Controlled Release Society, 217, 293–299. https://doi.org/10.1016/j.jconrel.2015.09.044
994. Prasad, P., Molla, M. R., Cui, W., Canakci, M., Osborne, B., Mager, J., & Thayumanavan, S. (2015). Polyamide Nanogels from Generally Recognized as Safe Components and Their Toxicity in Mouse Preimplantation Embryos. Biomacromolecules, 16(11), 3491–3498. https://doi.org/10.1021/acs.biomac.5b00900
995. Fang, R. H., Kroll, A. V., & Zhang, L. (2015). Nanoparticle-Based Manipulation of Antigen-Presenting Cells for Cancer Immunotherapy. Small (Weinheim an der Bergstrasse, Germany), 11(41), 5483–5496. https://doi.org/10.1002/smll.201501284
996. Nguyen, C. T., Tran, T. H., Amiji, M., Lu, X., & Kasi, R. M. (2015). Redox-sensitive nanoparticles from amphiphilic cholesterol-based block copolymers for enhanced tumor intracellular release of doxorubicin. Nanomedicine : nanotechnology, biology, and medicine, 11(8), 2071–2082. https://doi.org/10.1016/j.nano.2015.06.011
997. Stylianopoulos, T., & Jain, R. K. (2015). Design considerations for nanotherapeutics in oncology. Nanomedicine : nanotechnology, biology, and medicine, 11(8), 1893–1907. https://doi.org/10.1016/j.nano.2015.07.015
998. Tyagi, N., Tyagi, M., Pachauri, M., & Ghosh, P. C. (2015). Potential therapeutic applications of plant toxin-ricin in cancer: challenges and advances. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 36(11), 8239–8246. https://doi.org/10.1007/s13277-015-4028-4
999. Glasgow, M. D., & Chougule, M. B. (2015). Recent Developments in Active Tumor Targeted Multifunctional Nanoparticles for Combination Chemotherapy in Cancer Treatment and Imaging. Journal of biomedical nanotechnology, 11(11), 1859–1898. https://doi.org/10.1166/jbn.2015.2145
1000. Thu, H. P., Nam, N. H., Quang, B. T., Son, H. A., Toan, N. L., & Quang, D. T. (2015). In vitro and in vivo targeting effect of folate decorated paclitaxel loaded PLA-TPGS nanoparticles. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 23(6), 683–688. https://doi.org/10.1016/j.jsps.2015.02.002
1001. Koudelka, K. J., Pitek, A. S., Manchester, M., & Steinmetz, N. F. (2015). Virus-Based Nanoparticles as Versatile Nanomachines. Annual review of virology, 2(1), 379–401. https://doi.org/10.1146/annurev-virology-100114-055141
1002. Liu, X., Miller, A. L., 2nd, Waletzki, B. E., Mamo, T. K., Yaszemski, M. J., & Lu, L. (2015). Hydrolysable core crosslinked particle for receptor-mediated pH-sensitive anticancer drug delivery. New journal of chemistry = Nouveau journal de chimie, 39(11), 8840–8847. https://doi.org/10.1039/C5NJ01404B
1003. Mei, L., Zhu, G., Qiu, L., Wu, C., Chen, H., Liang, H., Cansiz, S., Lv, Y., Zhang, X., & Tan, W. (2015). Self-assembled Multifunctional DNA Nanoflowers for the Circumvention of Multidrug Resistance in Targeted Anticancer Drug Delivery. Nano research, 8(11), 3447–3460. https://doi.org/10.1007/s12274-015-0841-8
1004. Betzer, O., Meir, R., Dreifuss, T., Shamalov, K., Motiei, M., Shwartz, A., Baranes, K., Cohen, C. J., Shraga-Heled, N., Ofir, R., Yadid, G., & Popovtzer, R. (2015). In-vitro Optimization of Nanoparticle-Cell Labeling Protocols for In-vivo Cell Tracking Applications. Scientific reports, 5, 15400. https://doi.org/10.1038/srep15400
1005. Qiu, J., Zhang, R., Li, J., Sang, Y., Tang, W., Rivera Gil, P., & Liu, H. (2015). Fluorescent graphene quantum dots as traceable, pH-sensitive drug delivery systems. International journal of nanomedicine, 10, 6709–6724. https://doi.org/10.2147/IJN.S91864
1006. Agarwal, R., Jurney, P., Raythatha, M., Singh, V., Sreenivasan, S. V., Shi, L., & Roy, K. (2015). Effect of shape, size, and aspect ratio on nanoparticle penetration and distribution inside solid tissues using 3D spheroid models. Advanced healthcare materials, 4(15), 2269–2280. https://doi.org/10.1002/adhm.201500441
1007. Shu, D., Li, H., Shu, Y., Xiong, G., Carson, W. E., 3rd, Haque, F., Xu, R., & Guo, P. (2015). Systemic Delivery of Anti-miRNA for Suppression of Triple Negative Breast Cancer Utilizing RNA Nanotechnology. ACS nano, 9(10), 9731–9740. https://doi.org/10.1021/acsnano.5b02471
1008. Song, Y., Kang, Y. J., Jung, H., Kim, H., Kang, S., & Cho, H. (2015). Lumazine Synthase Protein Nanoparticle-Gd(III)-DOTA Conjugate as a T1 contrast agent for high-field MRI. Scientific reports, 5, 15656. https://doi.org/10.1038/srep15656
1009. Liu, X., Wang, J., Xu, W., Ding, J., Shi, B., Huang, K., Zhuang, X., & Chen, X. (2015). Glutathione-degradable drug-loaded nanogel effectively and securely suppresses hepatoma in mouse model. International journal of nanomedicine, 10, 6587–6602. https://doi.org/10.2147/IJN.S90000
1010. Zheng, Y., Tang, Y., Bao, Z., Wang, H., Ren, F., Guo, M., Quan, H., & Jiang, C. (2015). FePt nanoparticles as a potential X-ray activated chemotherapy agent for HeLa cells. International journal of nanomedicine, 10, 6435–6444. https://doi.org/10.2147/IJN.S88458
1011. Mustafa, R., Luo, Y., Wu, Y., Guo, R., & Shi, X. (2015). Dendrimer-Functionalized Laponite Nanodisks as a Platform for Anticancer Drug Delivery. Nanomaterials (Basel, Switzerland), 5(4), 1716–1731. https://doi.org/10.3390/nano5041716
1012. Zhang, F., Cao, J., Chen, X., Yang, K., Zhu, L., Fu, G., Huang, X., & Chen, X. (2015). Noninvasive Dynamic Imaging of Tumor Early Response to Nanoparticle-mediated Photothermal Therapy. Theranostics, 5(12), 1444–1455. https://doi.org/10.7150/thno.13398
1013. Kunjachan, S., Ehling, J., Storm, G., Kiessling, F., & Lammers, T. (2015). Noninvasive Imaging of Nanomedicines and Nanotheranostics: Principles, Progress, and Prospects. Chemical reviews, 115(19), 10907–10937. https://doi.org/10.1021/cr500314d
1014. Chinen, A. B., Guan, C. M., Ferrer, J. R., Barnaby, S. N., Merkel, T. J., & Mirkin, C. A. (2015). Nanoparticle Probes for the Detection of Cancer Biomarkers, Cells, and Tissues by Fluorescence. Chemical reviews, 115(19), 10530–10574. https://doi.org/10.1021/acs.chemrev.5b00321
1015. Zhu, C. D., Zheng, Q., Wang, L. X., Xu, H. F., Tong, J. L., Zhang, Q. A., Wan, Y., & Wu, J. Q. (2015). Synthesis of novel galactose functionalized gold nanoparticles and its radiosensitizing mechanism. Journal of nanobiotechnology, 13, 67. https://doi.org/10.1186/s12951-015-0129-x
1016. Sun, W., Ji, W., Hall, J. M., Hu, Q., Wang, C., Beisel, C. L., & Gu, Z. (2015). Self-assembled DNA nanoclews for the efficient delivery of CRISPR-Cas9 for genome editing. Angewandte Chemie (International ed. in English), 54(41), 12029–12033. https://doi.org/10.1002/anie.201506030
1017. Wang, C., Wang, Y., Li, Y., Bodemann, B., Zhao, T., Ma, X., Huang, G., Hu, Z., DeBerardinis, R. J., White, M. A., & Gao, J. (2015). A nanobuffer reporter library for fine-scale imaging and perturbation of endocytic organelles. Nature communications, 6, 8524. https://doi.org/10.1038/ncomms9524
1018. Nouri, F. S., Banerjee, D., & Hatefi, A. (2015). Practical Issues with the Use of Stem Cells for Cancer Gene Therapy. Stem cell reviews and reports, 11(5), 688–698. https://doi.org/10.1007/s12015-015-9605-9
1019. Zhang, Z., & Ma, P. X. (2015). From Nanofibrous Hollow Microspheres to Nanofibrous Hollow Discs and Nanofibrous Shells. Macromolecular rapid communications, 36(19), 1735–1741. https://doi.org/10.1002/marc.201500342
1020. Dawidczyk, C. M., Russell, L. M., & Searson, P. C. (2015). Recommendations for Benchmarking Preclinical Studies of Nanomedicines. Cancer research, 75(19), 4016–4020. https://doi.org/10.1158/0008-5472.CAN-15-1558
1021. Stocke, N. A., Arnold, S. M., & Hilt, J. Z. (2015). Responsive Hydrogel Nanoparticles for Pulmonary Delivery. Journal of drug delivery science and technology, 29, 143–151. https://doi.org/10.1016/j.jddst.2015.06.013
1022. Lv, Y., Hu, R., Zhu, G., Zhang, X., Mei, L., Liu, Q., Qiu, L., Wu, C., & Tan, W. (2015). Preparation and biomedical applications of programmable and multifunctional DNA nanoflowers. Nature protocols, 10(10), 1508–1524. https://doi.org/10.1038/nprot.2015.078
1023. Affram, K., Udofot, O., Cat, A., & Agyare, E. (2015). In vitro and in vivo antitumor activity of gemcitabine loaded thermosensitive liposomal nanoparticles and mild hyperthermia in pancreatic cancer. International journal of advanced research, 3(10), 859–874.
1024. Zhang, S., Gao, H., & Bao, G. (2015). Physical Principles of Nanoparticle Cellular Endocytosis. ACS nano, 9(9), 8655–8671. https://doi.org/10.1021/acsnano.5b03184
1025. Conde J. (2015). The Golden Age in Cancer Nanobiotechnology: Quo Vadis?. Frontiers in bioengineering and biotechnology, 3, 142. https://doi.org/10.3389/fbioe.2015.00142
1026. Martins, P., Jesus, J., Santos, S., Raposo, L. R., Roma-Rodrigues, C., Baptista, P. V., & Fernandes, A. R. (2015). Heterocyclic Anticancer Compounds: Recent Advances and the Paradigm Shift towards the Use of Nanomedicine's Tool Box. Molecules (Basel, Switzerland), 20(9), 16852–16891. https://doi.org/10.3390/molecules200916852
1027. Tang, J., Li, L., Howard, C. B., Mahler, S. M., Huang, L., & Xu, Z. P. (2015). Preparation of optimized lipid-coated calcium phosphate nanoparticles for enhanced in vitro gene delivery to breast cancer cells. Journal of materials chemistry. B, 3(33), 6805–6812. https://doi.org/10.1039/C5TB00912J
1028. Saifullah, B., & Hussein, M. Z. (2015). Inorganic nanolayers: structure, preparation, and biomedical applications. International journal of nanomedicine, 10, 5609–5633. https://doi.org/10.2147/IJN.S72330
1029. Anselmo, A. C., & Mitragotri, S. (2015). A Review of Clinical Translation of Inorganic Nanoparticles. The AAPS journal, 17(5), 1041–1054. https://doi.org/10.1208/s12248-015-9780-2
1030. Gahlaut, N., Suarez, S., Uddin, M. I., Gordon, A. Y., Evans, S. M., & Jayagopal, A. (2015). Nanoengineering of therapeutics for retinal vascular disease. European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 95(Pt B), 323–330. https://doi.org/10.1016/j.ejpb.2015.05.001
1031. Meyer, R. A., Sunshine, J. C., & Green, J. J. (2015). Biomimetic particles as therapeutics. Trends in biotechnology, 33(9), 514–524. https://doi.org/10.1016/j.tibtech.2015.07.001
1032. Gobbo, O. L., Sjaastad, K., Radomski, M. W., Volkov, Y., & Prina-Mello, A. (2015). Magnetic Nanoparticles in Cancer Theranostics. Theranostics, 5(11), 1249–1263. https://doi.org/10.7150/thno.11544
1033. Zhang, J., Li, S., An, F. F., Liu, J., Jin, S., Zhang, J. C., Wang, P. C., Zhang, X., Lee, C. S., & Liang, X. J. (2015). Self-carried curcumin nanoparticles for in vitro and in vivo cancer therapy with real-time monitoring of drug release. Nanoscale, 7(32), 13503–13510. https://doi.org/10.1039/c5nr03259h
1034. Lee, H., Sung, D., Kim, J., Kim, B. T., Wang, T., An, S. S., Seo, S. W., & Yi, D. K. (2015). Silica nanoparticle-based dual imaging colloidal hybrids: cancer cell imaging and biodistribution. International journal of nanomedicine, 10 Spec Iss(Spec Iss), 215–225. https://doi.org/10.2147/IJN.S88311
1035. Song, L., Guo, Y., Roebuck, D., Chen, C., Yang, M., Yang, Z., Sreedharan, S., Glover, C., Thomas, J. A., Liu, D., Guo, S., Chen, R., & Zhou, D. (2015). Terminal PEGylated DNA-Gold Nanoparticle Conjugates Offering High Resistance to Nuclease Degradation and Efficient Intracellular Delivery of DNA Binding Agents. ACS applied materials & interfaces, 7(33), 18707–18716. https://doi.org/10.1021/acsami.5b05228
1036. Tran, T. H., Ramasamy, T., Choi, J. Y., Nguyen, H. T., Pham, T. T., Jeong, J. H., Ku, S. K., Choi, H. G., Yong, C. S., & Kim, J. O. (2015). Tumor-targeting, pH-sensitive nanoparticles for docetaxel delivery to drug-resistant cancer cells. International journal of nanomedicine, 10, 5249–5262. https://doi.org/10.2147/IJN.S89584
1037. Qu, M., Mehrmohammadi, M., & Emelianov, S. Y. (2015). Sensing the delivery and endocytosis of nanoparticles using magneto-photo-acoustic imaging. Photoacoustics, 3(3), 107–113. https://doi.org/10.1016/j.pacs.2015.08.004
1038. Misra, A. C., Luker, K. E., Durmaz, H., Luker, G. D., & Lahann, J. (2015). CXCR4-Targeted Nanocarriers for Triple Negative Breast Cancers. Biomacromolecules, 16(8), 2412–2417. https://doi.org/10.1021/acs.biomac.5b00653
1039. Hrynyk, M., Ellis, J. P., Haxho, F., Allison, S., Steele, J. A., Abdulkhalek, S., Neufeld, R. J., & Szewczuk, M. R. (2015). Therapeutic designed poly (lactic-co-glycolic acid) cylindrical oseltamivir phosphate-loaded implants impede tumor neovascularization, growth and metastasis in mouse model of human pancreatic carcinoma. Drug design, development and therapy, 9, 4573–4586. https://doi.org/10.2147/DDDT.S90170
1040. Meng, W. C., Pan, Y., & Zhao, X. (2015). Epirubicin-gold nanoparticles suppress hepatocellular carcinoma xenograft growth in nude mice. Journal of biomedical research, 29(6), 486–490. Advance online publication. https://doi.org/10.7555/JBR.29.20140044
1041. Anand, P., O'Neil, A., Lin, E., Douglas, T., & Holford, M. (2015). Tailored delivery of analgesic ziconotide across a blood brain barrier model using viral nanocontainers. Scientific reports, 5, 12497. https://doi.org/10.1038/srep12497
1042. Ganta, S., Singh, A., Kulkarni, P., Keeler, A. W., Piroyan, A., Sawant, R. R., Patel, N. R., Davis, B., Ferris, C., O'Neal, S., Zamboni, W., Amiji, M. M., & Coleman, T. P. (2015). EGFR Targeted Theranostic Nanoemulsion for Image-Guided Ovarian Cancer Therapy. Pharmaceutical research, 32(8), 2753–2763. https://doi.org/10.1007/s11095-015-1660-z
1043. Li, H., Rychahou, P. G., Cui, Z., Pi, F., Evers, B. M., Shu, D., Guo, P., & Luo, W. (2015). RNA Nanoparticles Derived from Three-Way Junction of Phi29 Motor pRNA Are Resistant to I-125 and Cs-131 Radiation. Nucleic acid therapeutics, 25(4), 188–197. https://doi.org/10.1089/nat.2014.0525
1044. Matsumoto, N. M., Buchman, G. W., Rome, L. H., & Maynard, H. D. (2015). Dual pH- and Temperature-Responsive Protein Nanoparticles. European polymer journal, 69, 532–539. https://doi.org/10.1016/j.eurpolymj.2015.01.043
1045. Rwei, A. Y., Wang, W., & Kohane, D. S. (2015). Photoresponsive nanoparticles for drug delivery. Nano today, 10(4), 451–467. https://doi.org/10.1016/j.nantod.2015.06.004
1046. Zhang, P., Cheetham, A. G., Lock, L. L., Li, Y., & Cui, H. (2015). Activatable nanoprobes for biomolecular detection. Current opinion in biotechnology, 34, 171–179. https://doi.org/10.1016/j.copbio.2015.01.009
1047. Korang-Yeboah, M., Gorantla, Y., Paulos, S. A., Sharma, P., Chaudhary, J., & Palaniappan, R. (2015). Polycaprolactone/maltodextrin nanocarrier for intracellular drug delivery: formulation, uptake mechanism, internalization kinetics, and subcellular localization. International journal of nanomedicine, 10, 4763–4781. https://doi.org/10.2147/IJN.S75101
1048. Mitragotri, S., Anderson, D. G., Chen, X., Chow, E. K., Ho, D., Kabanov, A. V., Karp, J. M., Kataoka, K., Mirkin, C. A., Petrosko, S. H., Shi, J., Stevens, M. M., Sun, S., Teoh, S., Venkatraman, S. S., Xia, Y., Wang, S., Gu, Z., & Xu, C. (2015). Accelerating the Translation of Nanomaterials in Biomedicine. ACS nano, 9(7), 6644–6654. https://doi.org/10.1021/acsnano.5b03569
1049. Pacardo, D. B., Neupane, B., Rikard, S. M., Lu, Y., Mo, R., Mishra, S. R., Tracy, J. B., Wang, G., Ligler, F. S., & Gu, Z. (2015). A dual wavelength-activatable gold nanorod complex for synergistic cancer treatment. Nanoscale, 7(28), 12096–12103. https://doi.org/10.1039/c5nr01568e
1050. Bao, C., Conde, J., Curtin, J., Artzi, N., Tian, F., & Cui, D. (2015). Bioresponsive antisense DNA gold nanobeacons as a hybrid in vivo theranostics platform for the inhibition of cancer cells and metastasis. Scientific reports, 5, 12297. https://doi.org/10.1038/srep12297
1051. Nievergelt, A. P., Erickson, B. W., Hosseini, N., Adams, J. D., & Fantner, G. E. (2015). Studying biological membranes with extended range high-speed atomic force microscopy. Scientific reports, 5, 11987. https://doi.org/10.1038/srep11987
1052. Choi, S. Y., Song, M. S., Ryu, P. D., Lam, A. T., Joo, S. W., & Lee, S. Y. (2015). Gold nanoparticles promote osteogenic differentiation in human adipose-derived mesenchymal stem cells through the Wnt/β-catenin signaling pathway. International journal of nanomedicine, 10, 4383–4392. https://doi.org/10.2147/IJN.S78775
1053. Ruenraroengsak, P., & Tetley, T. D. (2015). Differential bioreactivity of neutral, cationic and anionic polystyrene nanoparticles with cells from the human alveolar compartment: robust response of alveolar type 1 epithelial cells. Particle and fibre toxicology, 12, 19. https://doi.org/10.1186/s12989-015-0091-7
1054. Williford, J. M., Santos, J. L., Shyam, R., & Mao, H. Q. (2015). Shape Control in Engineering of Polymeric Nanoparticles for Therapeutic Delivery. Biomaterials science, 3(7), 894–907. https://doi.org/10.1039/C5BM00006H
1055. Cai, K., Yen, J., Yin, Q., Liu, Y., Song, Z., Lezmi, S., Zhang, Y., Yang, X., Helferich, W. G., & Cheng, J. (2015). Redox-Responsive Self-Assembled Chain-Shattering Polymeric Therapeutics. Biomaterials science, 3(7), 1061–1065. https://doi.org/10.1039/C4BM00452C
1056. Wang, D., Tu, C., Su, Y., Zhang, C., Greiser, U., Zhu, X., Yan, D., & Wang, W. (2015). Supramolecularly engineered phospholipids constructed by nucleobase molecular recognition: upgraded generation of phospholipids for drug delivery. Chemical science, 6(7), 3775–3787. https://doi.org/10.1039/c5sc01188d
1057. Tsai, J. L., Zou, T., Liu, J., Chen, T., Chan, A. O., Yang, C., Lok, C. N., & Che, C. M. (2015). Luminescent platinum(ii) complexes with self-assembly and anti-cancer properties: hydrogel, pH dependent emission color and sustained-release properties under physiological conditions. Chemical science, 6(7), 3823–3830. https://doi.org/10.1039/c4sc03635b
1058. Mastria, E. M., Chen, M., McDaniel, J. R., Li, X., Hyun, J., Dewhirst, M. W., & Chilkoti, A. (2015). Doxorubicin-conjugated polypeptide nanoparticles inhibit metastasis in two murine models of carcinoma. Journal of controlled release : official journal of the Controlled Release Society, 208, 52–58. https://doi.org/10.1016/j.jconrel.2015.01.033
1059. Premnath, P., Venkatakrishnan, K., & Tan, B. (2015). Programming cancer through phase-functionalized silicon based biomaterials. Scientific reports, 5, 10826. https://doi.org/10.1038/srep10826
1060. Mohammadpour, M., Jabbarvand, M., Hashemi, H., & Delrish, E. (2015). Prophylactic effect of topical silica nanoparticles as a novel antineovascularization agent for inhibiting corneal neovascularization following chemical burn. Advanced biomedical research, 4, 124. https://doi.org/10.4103/2277-9175.158039
1061. Krishnan, V., Xu, X., Kelly, D., Snook, A., Waldman, S. A., Mason, R. W., Jia, X., & Rajasekaran, A. K. (2015). CD19-Targeted Nanodelivery of Doxorubicin Enhances Therapeutic Efficacy in B-Cell Acute Lymphoblastic Leukemia. Molecular pharmaceutics, 12(6), 2101–2111. https://doi.org/10.1021/acs.molpharmaceut.5b00071
1062. Nair, M. S., Lee, M. M., Bonnegarde-Bernard, A., Wallace, J. A., Dean, D. H., Ostrowski, M. C., Burry, R. W., Boyaka, P. N., & Chan, M. K. (2015). Cry protein crystals: a novel platform for protein delivery. PloS one, 10(6), e0127669. https://doi.org/10.1371/journal.pone.0127669
1063. Danad, I., Fayad, Z. A., Willemink, M. J., & Min, J. K. (2015). New Applications of Cardiac Computed Tomography: Dual-Energy, Spectral, and Molecular CT Imaging. JACC. Cardiovascular imaging, 8(6), 710–723. https://doi.org/10.1016/j.jcmg.2015.03.005
1064. Fuhrmann, G., Herrmann, I. K., & Stevens, M. M. (2015). Cell-derived vesicles for drug therapy and diagnostics: opportunities and challenges. Nano today, 10(3), 397–409. https://doi.org/10.1016/j.nantod.2015.04.004
1065. Kim, C. S., Mout, R., Zhao, Y., Yeh, Y. C., Tang, R., Jeong, Y., Duncan, B., Hardy, J. A., & Rotello, V. M. (2015). Co-delivery of protein and small molecule therapeutics using nanoparticle-stabilized nanocapsules. Bioconjugate chemistry, 26(5), 950–954. https://doi.org/10.1021/acs.bioconjchem.5b00146
1066. Qiu, L., Hong, C. Y., & Pan, C. Y. (2015). Doxorubicin-loaded aromatic imine-contained amphiphilic branched star polymer micelles: synthesis, self-assembly, and drug delivery. International journal of nanomedicine, 10, 3623–3640. https://doi.org/10.2147/IJN.S78355
1067. Bakhshinejad B. (2015). Phage display and targeting peptides: surface functionalization of nanocarriers for delivery of small non-coding RNAs. Frontiers in genetics, 6, 178. https://doi.org/10.3389/fgene.2015.00178
1068. Zhang, H., Ma, Y., Xie, Y., An, Y., Huang, Y., Zhu, Z., & Yang, C. J. (2015). A controllable aptamer-based self-assembled DNA dendrimer for high affinity targeting, bioimaging and drug delivery. Scientific reports, 5, 10099. https://doi.org/10.1038/srep10099
1069. Migliaccio, N., Palmieri, C., Ruggiero, I., Fiume, G., Martucci, N. M., Scala, I., Quinto, I., Scala, G., Lamberti, A., & Arcari, P. (2015). B-cell receptor-guided delivery of peptide-siRNA complex for B-cell lymphoma therapy. Cancer cell international, 15, 50. https://doi.org/10.1186/s12935-015-0202-4
1070. Wong, A. D., Ye, M., Ulmschneider, M. B., & Searson, P. C. (2015). Quantitative Analysis of the Enhanced Permeation and Retention (EPR) Effect. PloS one, 10(5), e0123461. https://doi.org/10.1371/journal.pone.0123461
1071. Kesharwani, P., & Iyer, A. K. (2015). Recent advances in dendrimer-based nanovectors for tumor-targeted drug and gene delivery. Drug discovery today, 20(5), 536–547. https://doi.org/10.1016/j.drudis.2014.12.012
1072. Mo, R., Jiang, T., Sun, W., & Gu, Z. (2015). ATP-responsive DNA-graphene hybrid nanoaggregates for anticancer drug delivery. Biomaterials, 50, 67–74. https://doi.org/10.1016/j.biomaterials.2015.01.053
1073. Liu, M., Huang, G., Cong, Y., Tong, G., Lin, Z., Yin, Y., & Zhang, C. (2015). The preparation and characterization of micelles from poly(γ-glutamic acid)-graft-poly(L-lactide) and the cellular uptake thereof. Journal of materials science. Materials in medicine, 26(5), 187. https://doi.org/10.1007/s10856-015-5519-y
1074. Yu, H. Y., Eckmann, D. M., Ayyaswamy, P. S., & Radhakrishnan, R. (2015). Composite generalized Langevin equation for Brownian motion in different hydrodynamic and adhesion regimes. Physical review. E, Statistical, nonlinear, and soft matter physics, 91(5), 052303. https://doi.org/10.1103/PhysRevE.91.052303
1075. Wójcik, M., Lewandowski, W., Król, M., Pawłowski, K., Mieczkowski, J., Lechowski, R., & Zabielska, K. (2015). Enhancing anti-tumor efficacy of Doxorubicin by non-covalent conjugation to gold nanoparticles - in vitro studies on feline fibrosarcoma cell lines. PloS one, 10(4), e0124955. https://doi.org/10.1371/journal.pone.0124955
1076. Chaurasia, S. S., Lim, R. R., Lakshminarayanan, R., & Mohan, R. R. (2015). Nanomedicine approaches for corneal diseases. Journal of functional biomaterials, 6(2), 277–298. https://doi.org/10.3390/jfb6020277
1077. Sayour, E. J., Sanchez-Perez, L., Flores, C., & Mitchell, D. A. (2015). Bridging infectious disease vaccines with cancer immunotherapy: a role for targeted RNA based immunotherapeutics. Journal for immunotherapy of cancer, 3, 13. https://doi.org/10.1186/s40425-015-0058-0
1078. Maswadeh, H. M., Aljarbou, A. N., Alorainy, M. S., Rahmani, A. H., & Khan, M. A. (2015). Coadministration of doxorubicin and etoposide loaded in camel milk phospholipids liposomes showed increased antitumor activity in a murine model. International journal of nanomedicine, 10, 2847–2855. https://doi.org/10.2147/IJN.S80820
1079. Williams, R. M., Shah, J., Ng, B. D., Minton, D. R., Gudas, L. J., Park, C. Y., & Heller, D. A. (2015). Mesoscale nanoparticles selectively target the renal proximal tubule epithelium. Nano letters, 15(4), 2358–2364. https://doi.org/10.1021/nl504610d
1080. Huang, W., Wang, X., Shi, C., Guo, D., Xu, G., Wang, L., Bodman, A., & Luo, J. (2015). Fine-tuning vitamin E-containing telodendrimers for efficient delivery of gambogic acid in colon cancer treatment. Molecular pharmaceutics, 12(4), 1216–1229. https://doi.org/10.1021/acs.molpharmaceut.5b00051
1081. Tang, L., Yin, Q., Xu, Y., Zhou, Q., Cai, K., Yen, J., Dobrucki, L. W., & Cheng, J. (2015). Bioorthogonal Oxime Ligation Mediated In Vivo Cancer Targeting. Chemical science, 6(4), 2182–2186. https://doi.org/10.1039/C5SC00063G
1082. Zhang, W., Wang, G., Falconer, J. R., Baguley, B. C., Shaw, J. P., Liu, J., Xu, H., See, E., Sun, J., Aa, J., & Wu, Z. (2015). Strategies to maximize liposomal drug loading for a poorly water-soluble anticancer drug. Pharmaceutical research, 32(4), 1451–1461. https://doi.org/10.1007/s11095-014-1551-8
1083. Xu, X., Ho, W., Zhang, X., Bertrand, N., & Farokhzad, O. (2015). Cancer nanomedicine: from targeted delivery to combination therapy. Trends in molecular medicine, 21(4), 223–232. https://doi.org/10.1016/j.molmed.2015.01.001
1084. Ucisik, M. H., Küpcü, S., Breitwieser, A., Gelbmann, N., Schuster, B., & Sleytr, U. B. (2015). S-layer fusion protein as a tool functionalizing emulsomes and CurcuEmulsomes for antibody binding and targeting. Colloids and surfaces. B, Biointerfaces, 128, 132–139. https://doi.org/10.1016/j.colsurfb.2015.01.055
1085. Meyers, J. D., Cheng, Y., Broome, A. M., Agnes, R. S., Schluchter, M. D., Margevicius, S., Wang, X., Kenney, M. E., Burda, C., & Basilion, J. P. (2015). Peptide-Targeted Gold Nanoparticles for Photodynamic Therapy of Brain Cancer. Particle & particle systems characterization : measurement and description of particle properties and behavior in powders and other disperse systems, 32(4), 448–457. https://doi.org/10.1002/ppsc.201400119
1086. Lane, L. A., Qian, X., Smith, A. M., & Nie, S. (2015). Physical chemistry of nanomedicine: understanding the complex behaviors of nanoparticles in vivo. Annual review of physical chemistry, 66, 521–547. https://doi.org/10.1146/annurev-physchem-040513-103718
1087. Zhang, Y., Lundberg, P., Diether, M., Porsch, C., Janson, C., Lynd, N. A., Ducani, C., Malkoch, M., Malmström, E., Hawker, C. J., & Nyström, A. M. (2015). Histamine-functionalized copolymer micelles as a drug delivery system in 2D and 3D models of breast cancer. Journal of materials chemistry. B, 3(12), 2472–2486. https://doi.org/10.1039/C4TB02051K
1088. Poon, C., He, C., Liu, D., Lu, K., & Lin, W. (2015). Self-assembled nanoscale coordination polymers carrying oxaliplatin and gemcitabine for synergistic combination therapy of pancreatic cancer. Journal of controlled release : official journal of the Controlled Release Society, 201, 90–99. https://doi.org/10.1016/j.jconrel.2015.01.026
1089. Wei, T., Chen, C., Liu, J., Liu, C., Posocco, P., Liu, X., Cheng, Q., Huo, S., Liang, Z., Fermeglia, M., Pricl, S., Liang, X. J., Rocchi, P., & Peng, L. (2015). Anticancer drug nanomicelles formed by self-assembling amphiphilic dendrimer to combat cancer drug resistance. Proceedings of the National Academy of Sciences of the United States of America, 112(10), 2978–2983. https://doi.org/10.1073/pnas.1418494112
1090. Shin, D. H., Heo, M. B., & Lim, Y. T. (2015). Self-assembled polyelectrolyte nanoparticles as fluorophore-free contrast agents for multicolor optical imaging. Molecules (Basel, Switzerland), 20(3), 4369–4382. https://doi.org/10.3390/molecules20034369
1091. Eom, H. J., Jeong, J. S., & Choi, J. (2015). Effect of aspect ratio on the uptake and toxicity of hydroxylated-multi walled carbon nanotubes in the nematode, Caenorhabditis elegans. Environmental health and toxicology, 30, e2015001. https://doi.org/10.5620/eht.e2015001
1092. Abouelmagd, S. A., Sun, B., Chang, A. C., Ku, Y. J., & Yeo, Y. (2015). Release kinetics study of poorly water-soluble drugs from nanoparticles: are we doing it right?. Molecular pharmaceutics, 12(3), 997–1003. https://doi.org/10.1021/mp500817h
1093. Rahman, H. S., Rasedee, A., How, C. W., Zeenathul, N. A., Chartrand, M. S., Yeap, S. K., Abdul, A. B., Tan, S. W., Othman, H. H., Ajdari, Z., Namvar, F., Arulselvan, P., Fakurazi, S., Mehrbod, P., Daneshvar, N., & Begum, H. (2015). Antileukemic effect of zerumbone-loaded nanostructured lipid carrier in WEHI-3B cell-induced murine leukemia model. International journal of nanomedicine, 10, 1649–1666. https://doi.org/10.2147/IJN.S67113
1094. Mitchell, M. J., & King, M. R. (2015). Leukocytes as carriers for targeted cancer drug delivery. Expert opinion on drug delivery, 12(3), 375–392. https://doi.org/10.1517/17425247.2015.966684
1095. Luo, D., Carter, K. A., & Lovell, J. F. (2015). Nanomedical engineering: shaping future nanomedicines. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 7(2), 169–188. https://doi.org/10.1002/wnan.1315
1096. Ghaz-Jahanian, M. A., Abbaspour-Aghdam, F., Anarjan, N., Berenjian, A., & Jafarizadeh-Malmiri, H. (2015). Application of chitosan-based nanocarriers in tumor-targeted drug delivery. Molecular biotechnology, 57(3), 201–218. https://doi.org/10.1007/s12033-014-9816-3
1097. Kim, C., Tonga, G. Y., Yan, B., Kim, C. S., Kim, S. T., Park, M. H., Zhu, Z., Duncan, B., Creran, B., & Rotello, V. M. (2015). Regulating exocytosis of nanoparticles via host-guest chemistry. Organic & biomolecular chemistry, 13(8), 2474–2479. https://doi.org/10.1039/c4ob02433h
1098. Li, X., Gao, C., Wu, Y., Cheng, C. Y., Xia, W., & Zhang, Z. (2015). Combination delivery of Adjudin and Doxorubicin via integrating drug conjugation and nanocarrier approaches for the treatment of drug-resistant cancer cells. Journal of materials chemistry. B, 3(8), 1556–1564. https://doi.org/10.1039/c4tb01764a
1099. Waghela, B. N., Sharma, A., Dhumale, S., Pandey, S. M., & Pathak, C. (2015). Curcumin conjugated with PLGA potentiates sustainability, anti-proliferative activity and apoptosis in human colon carcinoma cells. PloS one, 10(2), e0117526. https://doi.org/10.1371/journal.pone.0117526
1100. Toporkiewicz, M., Meissner, J., Matusewicz, L., Czogalla, A., & Sikorski, A. F. (2015). Toward a magic or imaginary bullet? Ligands for drug targeting to cancer cells: principles, hopes, and challenges. International journal of nanomedicine, 10, 1399–1414. https://doi.org/10.2147/IJN.S74514
1101. Chiarelli, P. A., Kievit, F. M., Zhang, M., & Ellenbogen, R. G. (2015). Bionanotechnology and the future of glioma. Surgical neurology international, 6(Suppl 1), S45–S58. https://doi.org/10.4103/2152-7806.151334
1102. Jiang, T., Sun, W., Zhu, Q., Burns, N. A., Khan, S. A., Mo, R., & Gu, Z. (2015). Furin-mediated sequential delivery of anticancer cytokine and small-molecule drug shuttled by graphene. Advanced materials (Deerfield Beach, Fla.), 27(6), 1021–1028. https://doi.org/10.1002/adma.201404498
1103. Ediriwickrema, A., & Saltzman, W. M. (2015). Nanotherapy for Cancer: Targeting and Multifunctionality in the Future of Cancer Therapies. ACS biomaterials science & engineering, 1(2), 64–78. https://doi.org/10.1021/ab500084g
1104. Zhu, Y., Zhang, Y., Shi, G., Yang, J., Zhang, J., Li, W., Li, A., Tai, R., Fang, H., Fan, C., & Huang, Q. (2015). Nanodiamonds act as Trojan horse for intracellular delivery of metal ions to trigger cytotoxicity. Particle and fibre toxicology, 12, 2. https://doi.org/10.1186/s12989-014-0075-z
1105. Prabhu, R. H., Patravale, V. B., & Joshi, M. D. (2015). Polymeric nanoparticles for targeted treatment in oncology: current insights. International journal of nanomedicine, 10, 1001–1018. https://doi.org/10.2147/IJN.S56932
1106. Singh, R. S., Thakur, S. R., & Bansal, P. (2015). Algal lectins as promising biomolecules for biomedical research. Critical reviews in microbiology, 41(1), 77–88. https://doi.org/10.3109/1040841X.2013.798780
1107. Cho, H., Lai, T. C., Tomoda, K., & Kwon, G. S. (2015). Polymeric micelles for multi-drug delivery in cancer. AAPS PharmSciTech, 16(1), 10–20. https://doi.org/10.1208/s12249-014-0251-3
1108. Kumar, R., Belz, J., Markovic, S., Jadhav, T., Fowle, W., Niedre, M., Cormack, R., Makrigiorgos, M. G., & Sridhar, S. (2015). Nanoparticle-based brachytherapy spacers for delivery of localized combined chemoradiation therapy. International journal of radiation oncology, biology, physics, 91(2), 393–400. https://doi.org/10.1016/j.ijrobp.2014.10.041
1109. Petschauer, J. S., Madden, A. J., Kirschbrown, W. P., Song, G., & Zamboni, W. C. (2015). The effects of nanoparticle drug loading on the pharmacokinetics of anticancer agents. Nanomedicine (London, England), 10(3), 447–463. https://doi.org/10.2217/nnm.14.179
1110. Ma, M., Weng, M., Zhang, M., Qin, Y., Gong, W., & Quan, Z. (2015). Targeting gallbladder cancer: hyaluronan sensitizes cancer cells to chemo-therapeutics. International journal of clinical and experimental pathology, 8(2), 1822–1825.
1111. Zhang, X. Q., Even-Or, O., Xu, X., van Rosmalen, M., Lim, L., Gadde, S., Farokhzad, O. C., & Fisher, E. A. (2015). Nanoparticles containing a liver X receptor agonist inhibit inflammation and atherosclerosis. Advanced healthcare materials, 4(2), 228–236. https://doi.org/10.1002/adhm.201400337
1112. Liu, Y., Chen, C., Qian, P., Lu, X., Sun, B., Zhang, X., Wang, L., Gao, X., Li, H., Chen, Z., Tang, J., Zhang, W., Dong, J., Bai, R., Lobie, P. E., Wu, Q., Liu, S., Zhang, H., Zhao, F., Wicha, M. S., … Zhao, Y. (2015). Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor. Nature communications, 6, 5988. https://doi.org/10.1038/ncomms6988
1113. Li, Z., & Gorfe, A. A. (2015). Receptor-mediated membrane adhesion of lipid-polymer hybrid (LPH) nanoparticles studied by dissipative particle dynamics simulations. Nanoscale, 7(2), 814–824. https://doi.org/10.1039/c4nr04834b
1114. Black, K. C., Akers, W. J., Sudlow, G., Xu, B., Laforest, R., & Achilefu, S. (2015). Dual-radiolabeled nanoparticle SPECT probes for bioimaging. Nanoscale, 7(2), 440–444. https://doi.org/10.1039/c4nr05269b
1115. Yamamoto, H., Wu, X., Nakanishi, H., Yamamoto, Y., Uemura, M., Hata, T., Nishimura, J., Takemasa, I., Mizushima, T., Sasaki, J., Imazato, S., Matsuura, N., Doki, Y., & Mori, M. (2015). A glucose carbonate apatite complex exhibits in vitro and in vivo anti-tumour effects. Scientific reports, 5, 7742. https://doi.org/10.1038/srep07742
1116. Liu, J., Liu, W., Weitzhandler, I., Bhattacharyya, J., Li, X., Wang, J., Qi, Y., Bhattacharjee, S., & Chilkoti, A. (2015). Ring-opening polymerization of prodrugs: a versatile approach to prepare well-defined drug-loaded nanoparticles. Angewandte Chemie (International ed. in English), 54(3), 1002–1006. https://doi.org/10.1002/anie.201409293
1117. Wu, T. T., & Zhou, S. H. (2015). Nanoparticle-based targeted therapeutics in head-and-neck cancer. International journal of medical sciences, 12(2), 187–200. https://doi.org/10.7150/ijms.10083
1118. Kue, C. S., Kamkaew, A., Lee, H. B., Chung, L. Y., Kiew, L. V., & Burgess, K. (2015). Targeted PDT agent eradicates TrkC expressing tumors via photodynamic therapy (PDT). Molecular pharmaceutics, 12(1), 212–222. https://doi.org/10.1021/mp5005564
1119. Zhou, C., Chen, T., Wu, C., Zhu, G., Qiu, L., Cui, C., Hou, W., & Tan, W. (2015). Aptamer CaCO3 nanostructures: a facile, pH-responsive, specific platform for targeted anticancer theranostics. Chemistry, an Asian journal, 10(1), 166–171. https://doi.org/10.1002/asia.201403115
1120. Bugno, J., Hsu, H. J., & Hong, S. (2015). Tweaking dendrimers and dendritic nanoparticles for controlled nano-bio interactions: potential nanocarriers for improved cancer targeting. Journal of drug targeting, 23(7-8), 642–650. https://doi.org/10.3109/1061186X.2015.1052077
1121. Veiseh, O., Tang, B. C., Whitehead, K. A., Anderson, D. G., & Langer, R. (2015). Managing diabetes with nanomedicine: challenges and opportunities. Nature reviews. Drug discovery, 14(1), 45–57. https://doi.org/10.1038/nrd4477
1122. Taylor, K., Howard, C. B., Jones, M. L., Sedliarou, I., MacDiarmid, J., Brahmbhatt, H., Munro, T. P., & Mahler, S. M. (2015). Nanocell targeting using engineered bispecific antibodies. mAbs, 7(1), 53–65. https://doi.org/10.4161/19420862.2014.985952
1123. Chattopadhyay, S., Dash, S. K., Tripathy, S., Pramanik, P., & Roy, S. (2015). Phosphonomethyl iminodiacetic acid-conjugated cobalt oxide nanoparticles liberate Co(++) ion-induced stress associated activation of TNF-α/p38 MAPK/caspase 8-caspase 3 signaling in human leukemia cells. Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 20(1), 123–141. https://doi.org/10.1007/s00775-014-1221-7
1124. Meng, H., Wang, M., Liu, H., Liu, X., Situ, A., Wu, B., Ji, Z., Chang, C. H., & Nel, A. E. (2015). Use of a lipid-coated mesoporous silica nanoparticle platform for synergistic gemcitabine and paclitaxel delivery to human pancreatic cancer in mice. ACS nano, 9(4), 3540–3557. https://doi.org/10.1021/acsnano.5b00510
1125. Maswadeh, H. M., Aljarbou, A. N., Alorainy, M. S., Alsharidah, M. S., & Khan, M. A. (2015). Etoposide incorporated into camel milk phospholipids liposomes shows increased activity against fibrosarcoma in a mouse model. BioMed research international, 2015, 743051. https://doi.org/10.1155/2015/743051
1126. Tu, C., Das, S., Baker, A. B., Zoldan, J., & Suggs, L. J. (2015). Nanoscale strategies: treatment for peripheral vascular disease and critical limb ischemia. ACS nano, 9(4), 3436–3452. https://doi.org/10.1021/nn507269g
1127. Khan, S., Chauhan, N., Yallapu, M. M., Ebeling, M. C., Balakrishna, S., Ellis, R. T., Thompson, P. A., Balabathula, P., Behrman, S. W., Zafar, N., Singh, M. M., Halaweish, F. T., Jaggi, M., & Chauhan, S. C. (2015). Nanoparticle formulation of ormeloxifene for pancreatic cancer. Biomaterials, 53, 731–743. https://doi.org/10.1016/j.biomaterials.2015.02.082
1128. Shi, Y., Kunjachan, S., Wu, Z., Gremse, F., Moeckel, D., van Zandvoort, M., Kiessling, F., Storm, G., van Nostrum, C. F., Hennink, W. E., & Lammers, T. (2015). Fluorophore labeling of core-crosslinked polymeric micelles for multimodal in vivo and ex vivo optical imaging. Nanomedicine (London, England), 10(7), 1111–1125. https://doi.org/10.2217/nnm.14.170
1129. Chenel, V., Boissy, P., Cloarec, J. P., & Patenaude, J. (2015). Effects of disciplinary cultures of researchers and research trainees on the acceptability of nanocarriers for drug delivery in different contexts of use: a mixed-methods study. Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology, 17(4), 186. https://doi.org/10.1007/s11051-015-2998-1
1130. Sobczynski, D. J., Fish, M. B., Fromen, C. A., Carasco-Teja, M., Coleman, R. M., & Eniola-Adefeso, O. (2015). Drug carrier interaction with blood: a critical aspect for high-efficient vascular-targeted drug delivery systems. Therapeutic delivery, 6(8), 915–934. https://doi.org/10.4155/TDE.15.38
1131. Rahmani, S., Villa, C. H., Dishman, A. F., Grabowski, M. E., Pan, D. C., Durmaz, H., Misra, A. C., Colón-Meléndez, L., Solomon, M. J., Muzykantov, V. R., & Lahann, J. (2015). Long-circulating Janus nanoparticles made by electrohydrodynamic co-jetting for systemic drug delivery applications. Journal of drug targeting, 23(7-8), 750–758. https://doi.org/10.3109/1061186X.2015.1076428
1132. Salzano, G., Costa, D. F., & Torchilin, V. P. (2015). siRNA Delivery by Stimuli-Sensitive Nanocarriers. Current pharmaceutical design, 21(31), 4566–4573. https://doi.org/10.2174/138161282131151013190410
1133. Zare-Zardini, H., Amiri, A., Shanbedi, M., Taheri-Kafrani, A., Sadri, Z., Ghanizadeh, F., Neamatzadeh, H., Sheikhpour, R., Keyvani Boroujeni, F., Masoumi Dehshiri, R., Hashemi, A., Aminorroaya, M. M., Dehgahnzadeh, M. R., & Shahriari, S. h. (2015). Nanotechnology and Pediatric Cancer: Prevention, Diagnosis and Treatment. Iranian journal of pediatric hematology and oncology, 5(4), 233–248.
1134. Wang, Q., Zhang, C., Shen, G., Liu, H., Fu, H., & Cui, D. (2014). Fluorescent carbon dots as an efficient siRNA nanocarrier for its interference therapy in gastric cancer cells. Journal of nanobiotechnology, 12, 58. https://doi.org/10.1186/s12951-014-0058-0
1135. Zhao, X., Chen, Q., Liu, W., Li, Y., Tang, H., Liu, X., & Yang, X. (2014). Codelivery of doxorubicin and curcumin with lipid nanoparticles results in improved efficacy of chemotherapy in liver cancer. International journal of nanomedicine, 10, 257–270. https://doi.org/10.2147/IJN.S73322
1136. Luk, B. T., & Zhang, L. (2014). Current advances in polymer-based nanotheranostics for cancer treatment and diagnosis. ACS applied materials & interfaces, 6(24), 21859–21873. https://doi.org/10.1021/am5036225
1137. Moon, H., Lee, J., Kim, H., Heo, S., Min, J., & Kang, S. (2014). Genetically engineering encapsulin protein cage nanoparticle as a SCC-7 cell targeting optical nanoprobe. Biomaterials research, 18, 21. https://doi.org/10.1186/2055-7124-18-21
1138. Kleinstreuer, C., Feng, Y., & Childress, E. (2014). Drug-targeting methodologies with applications: A review. World journal of clinical cases, 2(12), 742–756. https://doi.org/10.12998/wjcc.v2.i12.742
1139. Williford, J. M., Ren, Y., Huang, K., Pan, D., & Mao, H. Q. (2014). Shape Transformation Following Reduction-Sensitive PEG Cleavage of Polymer/DNA Nanoparticles. Journal of materials chemistry. B, 2(46), 8106–8109. https://doi.org/10.1039/C4TB00967C
1140. Lu, Y., Mo, R., Tai, W., Sun, W., Pacardo, D. B., Qian, C., Shen, Q., Ligler, F. S., & Gu, Z. (2014). Self-folded redox/acid dual-responsive nanocarriers for anticancer drug delivery. Chemical communications (Cambridge, England), 50(95), 15105–15108. https://doi.org/10.1039/c4cc07004f
1141. Mhashal, A. R., & Roy, S. (2014). Effect of gold nanoparticle on structure and fluidity of lipid membrane. PloS one, 9(12), e114152. https://doi.org/10.1371/journal.pone.0114152
1142. Emoto, S., Sunami, E., Yamaguchi, H., Ishihara, S., Kitayama, J., & Watanabe, T. (2014). Drug development for intraperitoneal chemotherapy against peritoneal carcinomatosis from gastrointestinal cancer. Surgery today, 44(12), 2209–2220. https://doi.org/10.1007/s00595-014-0848-x
1143. Zhen, Z., Tang, W., Todd, T., & Xie, J. (2014). Ferritins as nanoplatforms for imaging and drug delivery. Expert opinion on drug delivery, 11(12), 1913–1922. https://doi.org/10.1517/17425247.2014.941354
1144. Hoch, U., Staschen, C. M., Johnson, R. K., & Eldon, M. A. (2014). Nonclinical pharmacokinetics and activity of etirinotecan pegol (NKTR-102), a long-acting topoisomerase 1 inhibitor, in multiple cancer models. Cancer chemotherapy and pharmacology, 74(6), 1125–1137. https://doi.org/10.1007/s00280-014-2577-7
1145. Song, G., Darr, D. B., Santos, C. M., Ross, M., Valdivia, A., Jordan, J. L., Midkiff, B. R., Cohen, S., Nikolaishvili-Feinberg, N., Miller, C. R., Tarrant, T. K., Rogers, A. B., Dudley, A. C., Perou, C. M., & Zamboni, W. C. (2014). Effects of tumor microenvironment heterogeneity on nanoparticle disposition and efficacy in breast cancer tumor models. Clinical cancer research : an official journal of the American Association for Cancer Research, 20(23), 6083–6095. https://doi.org/10.1158/1078-0432.CCR-14-0493
1146. Lai, Y. T., Reading, E., Hura, G. L., Tsai, K. L., Laganowsky, A., Asturias, F. J., Tainer, J. A., Robinson, C. V., & Yeates, T. O. (2014). Structure of a designed protein cage that self-assembles into a highly porous cube. Nature chemistry, 6(12), 1065–1071. https://doi.org/10.1038/nchem.2107
1147. Chitkara, D., Mittal, A., Mahato, R. I., & Kumar, N. (2014). Core-shell nanoparticulate formulation of gemcitabine: lyophilization, stability studies, and in vivo evaluation. Drug delivery and translational research, 4(5-6), 439–451. https://doi.org/10.1007/s13346-014-0206-y
1148. Yang, X., Wu, S., Wang, Y., Li, Y., Chang, D., Luo, Y., Ye, S., & Hou, Z. (2014). Evaluation of self-assembled HCPT-loaded PEG-b-PLA nanoparticles by comparing with HCPT-loaded PLA nanoparticles. Nanoscale research letters, 9(1), 2408. https://doi.org/10.1186/1556-276X-9-687
1149. Sun, W., Lu, Y., & Gu, Z. (2014). Advances in Anticancer Protein Delivery Using Micro-/ Nanoparticles. Particle & particle systems characterization : measurement and description of particle properties and behavior in powders and other disperse systems, 31(12), 1204–1222. https://doi.org/10.1002/ppsc.201400140
1150. Lu, Y., Sun, W., & Gu, Z. (2014). Stimuli-responsive nanomaterials for therapeutic protein delivery. Journal of controlled release : official journal of the Controlled Release Society, 194, 1–19. https://doi.org/10.1016/j.jconrel.2014.08.015
1151. Peddada, L. Y., Garbuzenko, O. B., Devore, D. I., Minko, T., & Roth, C. M. (2014). Delivery of antisense oligonucleotides using poly(alkylene oxide)-poly(propylacrylic acid) graft copolymers in conjunction with cationic liposomes. Journal of controlled release : official journal of the Controlled Release Society, 194, 103–112. https://doi.org/10.1016/j.jconrel.2014.08.023
1152. Pearson, R. M., Juettner, V. V., & Hong, S. (2014). Biomolecular corona on nanoparticles: a survey of recent literature and its implications in targeted drug delivery. Frontiers in chemistry, 2, 108. https://doi.org/10.3389/fchem.2014.00108
1153. Conniot, J., Silva, J. M., Fernandes, J. G., Silva, L. C., Gaspar, R., Brocchini, S., Florindo, H. F., & Barata, T. S. (2014). Cancer immunotherapy: nanodelivery approaches for immune cell targeting and tracking. Frontiers in chemistry, 2, 105. https://doi.org/10.3389/fchem.2014.00105
1154. Anselmo, A. C., Modery-Pawlowski, C. L., Menegatti, S., Kumar, S., Vogus, D. R., Tian, L. L., Chen, M., Squires, T. M., Sen Gupta, A., & Mitragotri, S. (2014). Platelet-like nanoparticles: mimicking shape, flexibility, and surface biology of platelets to target vascular injuries. ACS nano, 8(11), 11243–11253. https://doi.org/10.1021/nn503732m
1155. Thorley, A. J., Ruenraroengsak, P., Potter, T. E., & Tetley, T. D. (2014). Critical determinants of uptake and translocation of nanoparticles by the human pulmonary alveolar epithelium. ACS nano, 8(11), 11778–11789. https://doi.org/10.1021/nn505399e
1156. Xu, X., Farach-Carson, M. C., & Jia, X. (2014). Three-dimensional in vitro tumor models for cancer research and drug evaluation. Biotechnology advances, 32(7), 1256–1268. https://doi.org/10.1016/j.biotechadv.2014.07.009
1157. Hu, Q., Katti, P. S., & Gu, Z. (2014). Enzyme-responsive nanomaterials for controlled drug delivery. Nanoscale, 6(21), 12273–12286. https://doi.org/10.1039/c4nr04249b
1158. Chakravarty, R., Hong, H., & Cai, W. (2014). Positron emission tomography image-guided drug delivery: current status and future perspectives. Molecular pharmaceutics, 11(11), 3777–3797. https://doi.org/10.1021/mp500173s
1159. Shukla, P., Rao, G. M., Pandey, G., Sharma, S., Mittapelly, N., Shegokar, R., & Mishra, P. R. (2014). Therapeutic interventions in sepsis: current and anticipated pharmacological agents. British journal of pharmacology, 171(22), 5011–5031. https://doi.org/10.1111/bph.12829
1160. Roh, Y. H., Lee, J. B., Shopsowitz, K. E., Dreaden, E. C., Morton, S. W., Poon, Z., Hong, J., Yamin, I., Bonner, D. K., & Hammond, P. T. (2014). Layer-by-layer assembled antisense DNA microsponge particles for efficient delivery of cancer therapeutics. ACS nano, 8(10), 9767–9780. https://doi.org/10.1021/nn502596b
1161. Li, X., Robinson, S. M., Gupta, A., Saha, K., Jiang, Z., Moyano, D. F., Sahar, A., Riley, M. A., & Rotello, V. M. (2014). Functional gold nanoparticles as potent antimicrobial agents against multi-drug-resistant bacteria. ACS nano, 8(10), 10682–10686. https://doi.org/10.1021/nn5042625
1162. Tang, L., Yang, X., Yin, Q., Cai, K., Wang, H., Chaudhury, I., Yao, C., Zhou, Q., Kwon, M., Hartman, J. A., Dobrucki, I. T., Dobrucki, L. W., Borst, L. B., Lezmi, S., Helferich, W. G., Ferguson, A. L., Fan, T. M., & Cheng, J. (2014). Investigating the optimal size of anticancer nanomedicine. Proceedings of the National Academy of Sciences of the United States of America, 111(43), 15344–15349. https://doi.org/10.1073/pnas.1411499111
1163. Raskatov, J. A., Szablowski, J. O., & Dervan, P. B. (2014). Tumor xenograft uptake of a pyrrole-imidazole (Py-Im) polyamide varies as a function of cell line grafted. Journal of medicinal chemistry, 57(20), 8471–8476. https://doi.org/10.1021/jm500964c
1164. Wang, Y., Lin, F. X., Zhao, Y., Wang, M. Z., Ge, X. W., Gong, Z. X., Bao, D. D., & Gu, Y. F. (2014). The sustained-release behavior and in vitro and in vivo transfection of pEGFP-loaded core-shell-structured chitosan-based composite particles. International journal of nanomedicine, 9, 4965–4978. https://doi.org/10.2147/IJN.S58104
1165. Moyer, T. J., Finbloom, J. A., Chen, F., Toft, D. J., Cryns, V. L., & Stupp, S. I. (2014). pH and amphiphilic structure direct supramolecular behavior in biofunctional assemblies. Journal of the American Chemical Society, 136(42), 14746–14752. https://doi.org/10.1021/ja5042429
1166. Sun, W., Jiang, T., Lu, Y., Reiff, M., Mo, R., & Gu, Z. (2014). Cocoon-like self-degradable DNA nanoclew for anticancer drug delivery. Journal of the American Chemical Society, 136(42), 14722–14725. https://doi.org/10.1021/ja5088024
1167. Li, L., & Thayumanavan, S. (2014). Environment-dependent guest exchange in supramolecular hosts. Langmuir : the ACS journal of surfaces and colloids, 30(41), 12384–12390. https://doi.org/10.1021/la502760c
1168. Sivasubramanian, M., Hsia, Y., & Lo, L. W. (2014). Nanoparticle-facilitated functional and molecular imaging for the early detection of cancer. Frontiers in molecular biosciences, 1, 15. https://doi.org/10.3389/fmolb.2014.00015
1169. Tai, W., Mo, R., Di, J., Subramanian, V., Gu, X., Buse, J. B., & Gu, Z. (2014). Bio-inspired synthetic nanovesicles for glucose-responsive release of insulin. Biomacromolecules, 15(10), 3495–3502. https://doi.org/10.1021/bm500364a
1170. Sunoqrot, S., Bugno, J., Lantvit, D., Burdette, J. E., & Hong, S. (2014). Prolonged blood circulation and enhanced tumor accumulation of folate-targeted dendrimer-polymer hybrid nanoparticles. Journal of controlled release : official journal of the Controlled Release Society, 191, 115–122. https://doi.org/10.1016/j.jconrel.2014.05.006
1171. Fanciullino, R., Mollard, S., Correard, F., Giacometti, S., Serdjebi, C., Iliadis, A., & Ciccolini, J. (2014). Biodistribution, tumor uptake and efficacy of 5-FU-loaded liposomes: why size matters. Pharmaceutical research, 31(10), 2677–2684. https://doi.org/10.1007/s11095-014-1364-9
1172. Patel, A. R., Chougule, M., & Singh, M. (2014). EphA2 targeting pegylated nanocarrier drug delivery system for treatment of lung cancer. Pharmaceutical research, 31(10), 2796–2809. https://doi.org/10.1007/s11095-014-1377-4
1173. Kaushik, A., Jayant, R. D., Sagar, V., & Nair, M. (2014). The potential of magneto-electric nanocarriers for drug delivery. Expert opinion on drug delivery, 11(10), 1635–1646. https://doi.org/10.1517/17425247.2014.933803
1174. Gowda, R., Madhunapantula, S. V., Sharma, A., Kuzu, O. F., & Robertson, G. P. (2014). Nanolipolee-007, a novel nanoparticle-based drug containing leelamine for the treatment of melanoma. Molecular cancer therapeutics, 13(10), 2328–2340. https://doi.org/10.1158/1535-7163.MCT-14-0357
1175. Emblem, K. E., Farrar, C. T., Gerstner, E. R., Batchelor, T. T., Borra, R. J., Rosen, B. R., Sorensen, A. G., & Jain, R. K. (2014). Vessel caliber--a potential MRI biomarker of tumour response in clinical trials. Nature reviews. Clinical oncology, 11(10), 566–584. https://doi.org/10.1038/nrclinonc.2014.126
1176. Dadgar, N., Koohi Moftakhari Esfahani, M., Torabi, S., Alavi, S. E., & Akbarzadeh, A. (2014). Effects of nanoliposomal and pegylated nanoliposomal artemisinin in treatment of breast cancer. Indian journal of clinical biochemistry : IJCB, 29(4), 501–504. https://doi.org/10.1007/s12291-013-0389-x
1177. Bhavana, S. M., & Lakshmi, C. R. (2014). Oral oncoprevention by phytochemicals - a systematic review disclosing the therapeutic dilemma. Advanced pharmaceutical bulletin, 4(Suppl 1), 413–420. https://doi.org/10.5681/apb.2014.061
1178. Key, J., Kim, Y. S., Tatulli, F., Palange, A. L., O'Neill, B., Aryal, S., Ramirez, M., Liu, X., Ferrari, M., Munden, R., & Decuzzi, P. (2014). Opportunities for NanoTheranosis in Lung Cancer and Pulmonary Metastasis. Clinical and translational imaging, 2(5), 427–437. https://doi.org/10.1007/s40336-014-0078-7
1179. Khatri, S., Das, N. G., & Das, S. K. (2014). Effect of methotrexate conjugated PAMAM dendrimers on the viability of MES-SA uterine cancer cells. Journal of pharmacy & bioallied sciences, 6(4), 297–302. https://doi.org/10.4103/0975-7406.142963
1180. Anselmo, A. C., & Mitragotri, S. (2014). An overview of clinical and commercial impact of drug delivery systems. Journal of controlled release : official journal of the Controlled Release Society, 190, 15–28. https://doi.org/10.1016/j.jconrel.2014.03.053
1181. Anselmo, A. C., & Mitragotri, S. (2014). Cell-mediated delivery of nanoparticles: taking advantage of circulatory cells to target nanoparticles. Journal of controlled release : official journal of the Controlled Release Society, 190, 531–541. https://doi.org/10.1016/j.jconrel.2014.03.050
1182. Gizzatov, A., Stigliano, C., Ananta, J. S., Sethi, R., Xu, R., Guven, A., Ramirez, M., Shen, H., Sood, A., Ferrari, M., Wilson, L. J., Liu, X., & Decuzzi, P. (2014). Geometrical confinement of Gd(DOTA) molecules within mesoporous silicon nanoconstructs for MR imaging of cancer. Cancer letters, 352(1), 97–101. https://doi.org/10.1016/j.canlet.2014.06.001
1183. Anikeeva, N., Sykulev, Y., Delikatny, E. J., & Popov, A. V. (2014). Core-based lipid nanoparticles as a nanoplatform for delivery of near-infrared fluorescent imaging agents. American journal of nuclear medicine and molecular imaging, 4(6), 507–524.
1184. Xue, W., Dahlman, J. E., Tammela, T., Khan, O. F., Sood, S., Dave, A., Cai, W., Chirino, L. M., Yang, G. R., Bronson, R., Crowley, D. G., Sahay, G., Schroeder, A., Langer, R., Anderson, D. G., & Jacks, T. (2014). Small RNA combination therapy for lung cancer. Proceedings of the National Academy of Sciences of the United States of America, 111(34), E3553–E3561. https://doi.org/10.1073/pnas.1412686111
1185. Wang, J., Zhu, R., Sun, X., Zhu, Y., Liu, H., & Wang, S. L. (2014). Intracellular uptake of etoposide-loaded solid lipid nanoparticles induces an enhancing inhibitory effect on gastric cancer through mitochondria-mediated apoptosis pathway. International journal of nanomedicine, 9, 3987–3998. https://doi.org/10.2147/IJN.S64103
1186. Yokoi, K., Kojic, M., Milosevic, M., Tanei, T., Ferrari, M., & Ziemys, A. (2014). Capillary-wall collagen as a biophysical marker of nanotherapeutic permeability into the tumor microenvironment. Cancer research, 74(16), 4239–4246. https://doi.org/10.1158/0008-5472.CAN-13-3494
1187. Sun, H., Meng, F., Cheng, R., Deng, C., & Zhong, Z. (2014). Reduction-responsive polymeric micelles and vesicles for triggered intracellular drug release. Antioxidants & redox signaling, 21(5), 755–767. https://doi.org/10.1089/ars.2013.5733
1188. Dawidczyk, C. M., Kim, C., Park, J. H., Russell, L. M., Lee, K. H., Pomper, M. G., & Searson, P. C. (2014). State-of-the-art in design rules for drug delivery platforms: lessons learned from FDA-approved nanomedicines. Journal of controlled release : official journal of the Controlled Release Society, 187, 133–144. https://doi.org/10.1016/j.jconrel.2014.05.036
1189. Lin, Y., & Hamme Ii, A. T. (2014). Targeted highly sensitive detection/eradication of multi-drug resistant Salmonella DT104 through gold nanoparticle-SWCNT bioconjugated nanohybrids. The Analyst, 139(15), 3702–3705. https://doi.org/10.1039/c4an00744a
1190. Bao, G., Bazilevs, Y., Chung, J. H., Decuzzi, P., Espinosa, H. D., Ferrari, M., Gao, H., Hossain, S. S., Hughes, T. J., Kamm, R. D., Liu, W. K., Marsden, A., & Schrefler, B. (2014). USNCTAM perspectives on mechanics in medicine. Journal of the Royal Society, Interface, 11(97), 20140301. https://doi.org/10.1098/rsif.2014.0301
1191. Pan-In, P., Wanichwecharungruang, S., Hanes, J., & Kim, A. J. (2014). Cellular trafficking and anticancer activity of Garcinia mangostana extract-encapsulated polymeric nanoparticles. International journal of nanomedicine, 9, 3677–3686. https://doi.org/10.2147/IJN.S66511
1192. Tai, W., Mo, R., Lu, Y., Jiang, T., & Gu, Z. (2014). Folding graft copolymer with pendant drug segments for co-delivery of anticancer drugs. Biomaterials, 35(25), 7194–7203. https://doi.org/10.1016/j.biomaterials.2014.05.004
1193. Lin, J., Shigdar, S., Fang, D. Z., Xiang, D., Wei, M. Q., Danks, A., Kong, L., Li, L., Qiao, L., & Duan, W. (2014). Improved efficacy and reduced toxicity of doxorubicin encapsulated in sulfatide-containing nanoliposome in a glioma model. PloS one, 9(7), e103736. https://doi.org/10.1371/journal.pone.0103736
1194. Luo, F., Li, Y., Jia, M., Cui, F., Wu, H., Yu, F., Lin, J., Yang, X., Hou, Z., & Zhang, Q. (2014). Validation of a Janus role of methotrexate-based PEGylated chitosan nanoparticles in vitro. Nanoscale research letters, 9(1), 363. https://doi.org/10.1186/1556-276X-9-363
1195. Marrache, S., Pathak, R. K., & Dhar, S. (2014). Detouring of cisplatin to access mitochondrial genome for overcoming resistance. Proceedings of the National Academy of Sciences of the United States of America, 111(29), 10444–10449. https://doi.org/10.1073/pnas.1405244111
1196. Gao, W., Lin, Z., Chen, M., Yang, X., Cui, Z., Zhang, X., Yuan, L., & Zhang, Q. (2014). The co-delivery of a low-dose P-glycoprotein inhibitor with doxorubicin sterically stabilized liposomes against breast cancer with low P-glycoprotein expression. International journal of nanomedicine, 9, 3425–3437. https://doi.org/10.2147/IJN.S56070
1197. Wang, Y., Shim, M. S., Levinson, N. S., Sung, H. W., & Xia, Y. (2014). Stimuli-Responsive Materials for Controlled Release of Theranostic Agents. Advanced functional materials, 24(27), 4206–4220. https://doi.org/10.1002/adfm.201400279
1198. Guan, S. S., Chang, J., Cheng, C. C., Luo, T. Y., Ho, A. S., Wang, C. C., Wu, C. T., & Liu, S. H. (2014). Afatinib and its encapsulated polymeric micelles inhibits HER2-overexpressed colorectal tumor cell growth in vitro and in vivo. Oncotarget, 5(13), 4868–4880. https://doi.org/10.18632/oncotarget.2050
1199. Shao, Y., Shi, C., Xu, G., Guo, D., & Luo, J. (2014). Photo and redox dual responsive reversibly cross-linked nanocarrier for efficient tumor-targeted drug delivery. ACS applied materials & interfaces, 6(13), 10381–10392. https://doi.org/10.1021/am501913m
1200. Quadir, M. A., Morton, S. W., Deng, Z. J., Shopsowitz, K. E., Murphy, R. P., Epps, T. H., 3rd, & Hammond, P. T. (2014). PEG-polypeptide block copolymers as pH-responsive endosome-solubilizing drug nanocarriers. Molecular pharmaceutics, 11(7), 2420–2430. https://doi.org/10.1021/mp500162w
1201. Suffredini, G., East, J. E., & Levy, L. M. (2014). New applications of nanotechnology for neuroimaging. AJNR. American journal of neuroradiology, 35(7), 1246–1253. https://doi.org/10.3174/ajnr.A3543
1202. Palange, A. L., Di Mascolo, D., Carallo, C., Gnasso, A., & Decuzzi, P. (2014). Lipid-polymer nanoparticles encapsulating curcumin for modulating the vascular deposition of breast cancer cells. Nanomedicine : nanotechnology, biology, and medicine, 10(5), 991–1002. https://doi.org/10.1016/j.nano.2014.02.004
1203. Blanco, E., Sangai, T., Wu, S., Hsiao, A., Ruiz-Esparza, G. U., Gonzalez-Delgado, C. A., Cara, F. E., Granados-Principal, S., Evans, K. W., Akcakanat, A., Wang, Y., Do, K. A., Meric-Bernstam, F., & Ferrari, M. (2014). Colocalized delivery of rapamycin and paclitaxel to tumors enhances synergistic targeting of the PI3K/Akt/mTOR pathway. Molecular therapy : the journal of the American Society of Gene Therapy, 22(7), 1310–1319. https://doi.org/10.1038/mt.2014.27
1204. Lukianova-Hleb, E. Y., Ren, X., Sawant, R. R., Wu, X., Torchilin, V. P., & Lapotko, D. O. (2014). On-demand intracellular amplification of chemoradiation with cancer-specific plasmonic nanobubbles. Nature medicine, 20(7), 778–784. https://doi.org/10.1038/nm.3484
1205. Bedi, D., Gillespie, J. W., & Petrenko, V. A. (2014). Selection of pancreatic cancer cell-binding landscape phages and their use in development of anticancer nanomedicines. Protein engineering, design & selection : PEDS, 27(7), 235–243. https://doi.org/10.1093/protein/gzu020
1206. Alexis F. (2014). Nano-polypharmacy to treat tumors: coencapsulation of drug combinations using nanoparticle technology. Molecular therapy : the journal of the American Society of Gene Therapy, 22(7), 1239–1240. https://doi.org/10.1038/mt.2014.96
1207. Jeelani, S., Reddy, R. C., Maheswaran, T., Asokan, G. S., Dany, A., & Anand, B. (2014). Theranostics: A treasured tailor for tomorrow. Journal of pharmacy & bioallied sciences, 6(Suppl 1), S6–S8. https://doi.org/10.4103/0975-7406.137249
1208. Baskaran, R., Madheswaran, T., Sundaramoorthy, P., Kim, H. M., & Yoo, B. K. (2014). Entrapment of curcumin into monoolein-based liquid crystalline nanoparticle dispersion for enhancement of stability and anticancer activity. International journal of nanomedicine, 9, 3119–3130. https://doi.org/10.2147/IJN.S61823
1209. Qhattal, H. S., Hye, T., Alali, A., & Liu, X. (2014). Hyaluronan polymer length, grafting density, and surface poly(ethylene glycol) coating influence in vivo circulation and tumor targeting of hyaluronan-grafted liposomes. ACS nano, 8(6), 5423–5440. https://doi.org/10.1021/nn405839n
1210. Baldi, G., Ravagli, C., Mazzantini, F., Loudos, G., Adan, J., Masa, M., Psimadas, D., Fragogeorgi, E. A., Locatelli, E., Innocenti, C., Sangregorio, C., & Comes Franchini, M. (2014). In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles. International journal of nanomedicine, 9, 3037–3056. https://doi.org/10.2147/IJN.S61273
1211. Nakano, T., Chin, C., Myint, D. M., Tan, E. W., Hale, P. J., Krishna M, B. M., Reynolds, J. N., Wickens, J., & Dani, K. M. (2014). Mimicking subsecond neurotransmitter dynamics with femtosecond laser stimulated nanosystems. Scientific reports, 4, 5398. https://doi.org/10.1038/srep05398
1212. Sun, Z., Worden, M., Wroczynskyj, Y., Yathindranath, V., van Lierop, J., Hegmann, T., & Miller, D. W. (2014). Magnetic field enhanced convective diffusion of iron oxide nanoparticles in an osmotically disrupted cell culture model of the blood-brain barrier. International journal of nanomedicine, 9, 3013–3026. https://doi.org/10.2147/IJN.S62260
1213. Pathak, R. K., McNitt, C. D., Popik, V. V., & Dhar, S. (2014). Copper-free click-chemistry platform to functionalize cisplatin prodrugs. Chemistry (Weinheim an der Bergstrasse, Germany), 20(23), 6861–6865. https://doi.org/10.1002/chem.201402573
1214. Wang, Z., Niu, G., & Chen, X. (2014). Polymeric materials for theranostic applications. Pharmaceutical research, 31(6), 1358–1376. https://doi.org/10.1007/s11095-013-1103-7
1215. Lee, T. R., Greene, M. S., Jiang, Z., Kopacz, A. M., Decuzzi, P., Chen, W., & Liu, W. K. (2014). Quantifying uncertainties in the microvascular transport of nanoparticles. Biomechanics and modeling in mechanobiology, 13(3), 515–526. https://doi.org/10.1007/s10237-013-0513-0
1216. Zhang, S., Wu, J., Wang, H., Wang, T., Jin, L., Shu, D., Shan, W., & Xiong, S. (2014). Liposomal oxymatrine in hepatic fibrosis treatment: formulation, in vitro and in vivo assessment. AAPS PharmSciTech, 15(3), 620–629. https://doi.org/10.1208/s12249-014-0086-y
1217. Singhana, B., Slattery, P., Chen, A., Wallace, M., & Melancon, M. P. (2014). Light-activatable gold nanoshells for drug delivery applications. AAPS PharmSciTech, 15(3), 741–752. https://doi.org/10.1208/s12249-014-0097-8
1218. Wang, D., Lin, B., & Ai, H. (2014). Theranostic nanoparticles for cancer and cardiovascular applications. Pharmaceutical research, 31(6), 1390–1406. https://doi.org/10.1007/s11095-013-1277-z
1219. Theek, B., Gremse, F., Kunjachan, S., Fokong, S., Pola, R., Pechar, M., Deckers, R., Storm, G., Ehling, J., Kiessling, F., & Lammers, T. (2014). Characterizing EPR-mediated passive drug targeting using contrast-enhanced functional ultrasound imaging. Journal of controlled release : official journal of the Controlled Release Society, 182, 83–89. https://doi.org/10.1016/j.jconrel.2014.03.007
1220. Bhirde, A. A., Chikkaveeraiah, B. V., Srivatsan, A., Niu, G., Jin, A. J., Kapoor, A., Wang, Z., Patel, S., Patel, V., Gorbach, A. M., Leapman, R. D., Gutkind, J. S., Hight Walker, A. R., & Chen, X. (2014). Targeted therapeutic nanotubes influence the viscoelasticity of cancer cells to overcome drug resistance. ACS nano, 8(5), 4177–4189. https://doi.org/10.1021/nn501223q
1221. Black, K. C., Wang, Y., Luehmann, H. P., Cai, X., Xing, W., Pang, B., Zhao, Y., Cutler, C. S., Wang, L. V., Liu, Y., & Xia, Y. (2014). Radioactive 198Au-doped nanostructures with different shapes for in vivo analyses of their biodistribution, tumor uptake, and intratumoral distribution. ACS nano, 8(5), 4385–4394. https://doi.org/10.1021/nn406258m
1222. Fajardo-Ortiz, D., Duran, L., Moreno, L., Ochoa, H., & Castaño, V. M. (2014). Liposomes versus metallic nanostructures: differences in the process of knowledge translation in cancer. International journal of nanomedicine, 9, 2627–2634. https://doi.org/10.2147/IJN.S62315
1223. Orecchioni, M., Bedognetti, D., Sgarrella, F., Marincola, F. M., Bianco, A., & Delogu, L. G. (2014). Impact of carbon nanotubes and graphene on immune cells. Journal of translational medicine, 12, 138. https://doi.org/10.1186/1479-5876-12-138
1224. Ye, W. L., Du, J. B., Zhang, B. L., Na, R., Song, Y. F., Mei, Q. B., Zhao, M. G., & Zhou, S. Y. (2014). Cellular uptake and antitumor activity of DOX-hyd-PEG-FA nanoparticles. PloS one, 9(5), e97358. https://doi.org/10.1371/journal.pone.0097358
1225. Basha, R., Sabnis, N., Heym, K., Bowman, W. P., & Lacko, A. G. (2014). Targeted nanoparticles for pediatric leukemia therapy. Frontiers in oncology, 4, 101. https://doi.org/10.3389/fonc.2014.00101
1226. Minami, K., Okamoto, K., Doi, K., Harano, K., Noiri, E., & Nakamura, E. (2014). siRNA delivery targeting to the lung via agglutination-induced accumulation and clearance of cationic tetraamino fullerene. Scientific reports, 4, 4916. https://doi.org/10.1038/srep04916
1227. Ando, D., Zandi, R., Kim, Y. W., Colvin, M., Rexach, M., & Gopinathan, A. (2014). Nuclear pore complex protein sequences determine overall copolymer brush structure and function. Biophysical journal, 106(9), 1997–2007. https://doi.org/10.1016/j.bpj.2014.03.021
1228. Zhao, L., Su, R., Cui, W., Shi, Y., Liu, L., & Su, C. (2014). Preparation of biocompatible heat-labile enterotoxin subunit B-bovine serum albumin nanoparticles for improving tumor-targeted drug delivery via heat-labile enterotoxin subunit B mediation. International journal of nanomedicine, 9, 2149–2156. https://doi.org/10.2147/IJN.S60764
1229. Dickerson, M., Winquist, N., & Bae, Y. (2014). Photo-inducible crosslinked nanoassemblies for pH-controlled drug release. Pharmaceutical research, 31(5), 1254–1263. https://doi.org/10.1007/s11095-013-1246-6
1230. Son, D., Lee, J., Qiao, S., Ghaffari, R., Kim, J., Lee, J. E., Song, C., Kim, S. J., Lee, D. J., Jun, S. W., Yang, S., Park, M., Shin, J., Do, K., Lee, M., Kang, K., Hwang, C. S., Lu, N., Hyeon, T., & Kim, D. H. (2014). Multifunctional wearable devices for diagnosis and therapy of movement disorders. Nature nanotechnology, 9(5), 397–404. https://doi.org/10.1038/nnano.2014.38
1231. Chan, K. W., Yu, T., Qiao, Y., Liu, Q., Yang, M., Patel, H., Liu, G., Kinzler, K. W., Vogelstein, B., Bulte, J. W., van Zijl, P. C., Hanes, J., Zhou, S., & McMahon, M. T. (2014). A diaCEST MRI approach for monitoring liposomal accumulation in tumors. Journal of controlled release : official journal of the Controlled Release Society, 180, 51–59. https://doi.org/10.1016/j.jconrel.2014.02.005
1232. Jhaveri, A. M., & Torchilin, V. P. (2014). Multifunctional polymeric micelles for delivery of drugs and siRNA. Frontiers in pharmacology, 5, 77. https://doi.org/10.3389/fphar.2014.00077
1233. Liao, L., Liu, J., Dreaden, E. C., Morton, S. W., Shopsowitz, K. E., Hammond, P. T., & Johnson, J. A. (2014). A convergent synthetic platform for single-nanoparticle combination cancer therapy: ratiometric loading and controlled release of cisplatin, doxorubicin, and camptothecin. Journal of the American Chemical Society, 136(16), 5896–5899. https://doi.org/10.1021/ja502011g
1234. Xu, Z., Wang, Y., Zhang, L., & Huang, L. (2014). Nanoparticle-delivered transforming growth factor-β siRNA enhances vaccination against advanced melanoma by modifying tumor microenvironment. ACS nano, 8(4), 3636–3645. https://doi.org/10.1021/nn500216y
1235. Bogart, L. K., Pourroy, G., Murphy, C. J., Puntes, V., Pellegrino, T., Rosenblum, D., Peer, D., & Lévy, R. (2014). Nanoparticles for imaging, sensing, and therapeutic intervention. ACS nano, 8(4), 3107–3122. https://doi.org/10.1021/nn500962q
1236. Hira, S. K., Mishra, A. K., Ray, B., & Manna, P. P. (2014). Targeted delivery of doxorubicin-loaded poly (ε-caprolactone)-b-poly (N-vinylpyrrolidone) micelles enhances antitumor effect in lymphoma. PloS one, 9(4), e94309. https://doi.org/10.1371/journal.pone.0094309
1237. Fan, Z., Dai, X., Lu, Y., Yu, E., Brahmbatt, N., Carter, N., Tchouwou, C., Singh, A. K., Jones, Y., Yu, H., & Ray, P. C. (2014). Enhancing targeted tumor treatment by near IR light-activatable photodynamic-photothermal synergistic therapy. Molecular pharmaceutics, 11(4), 1109–1116. https://doi.org/10.1021/mp4002816
1238. Peng, J., Qi, T., Liao, J., Chu, B., Yang, Q., Qu, Y., Li, W., Li, H., Luo, F., & Qian, Z. (2014). Mesoporous magnetic gold "nanoclusters" as theranostic carrier for chemo-photothermal co-therapy of breast cancer. Theranostics, 4(7), 678–692. https://doi.org/10.7150/thno.7869
1239. Carter, K. A., Shao, S., Hoopes, M. I., Luo, D., Ahsan, B., Grigoryants, V. M., Song, W., Huang, H., Zhang, G., Pandey, R. K., Geng, J., Pfeifer, B. A., Scholes, C. P., Ortega, J., Karttunen, M., & Lovell, J. F. (2014). Porphyrin-phospholipid liposomes permeabilized by near-infrared light. Nature communications, 5, 3546. https://doi.org/10.1038/ncomms4546
1240. Charoenphol, P., & Bermudez, H. (2014). Design and application of multifunctional DNA nanocarriers for therapeutic delivery. Acta biomaterialia, 10(4), 1683–1691. https://doi.org/10.1016/j.actbio.2013.07.021
1241. Liang, Y., & Kiick, K. L. (2014). Heparin-functionalized polymeric biomaterials in tissue engineering and drug delivery applications. Acta biomaterialia, 10(4), 1588–1600. https://doi.org/10.1016/j.actbio.2013.07.031
1242. Yu, Y., Huang, T., Wu, Y., Ma, X., Yu, G., & Qi, J. (2014). In-vitro and in-vivo imaging of prostate tumor using NaYF4: Yb, Er up-converting nanoparticles. Pathology oncology research : POR, 20(2), 335–341. https://doi.org/10.1007/s12253-013-9700-7
1243. Wang, S., Su, R., Nie, S., Sun, M., Zhang, J., Wu, D., & Moustaid-Moussa, N. (2014). Application of nanotechnology in improving bioavailability and bioactivity of diet-derived phytochemicals. The Journal of nutritional biochemistry, 25(4), 363–376. https://doi.org/10.1016/j.jnutbio.2013.10.002
1244. Gao, H., Hu, G., Zhang, Q., Zhang, S., Jiang, X., & He, Q. (2014). Pretreatment with chemotherapeutics for enhanced nanoparticles accumulation in tumor: the potential role of G2 cycle retention effect. Scientific reports, 4, 4492. https://doi.org/10.1038/srep04492
1245. Yurgel, V. C., Oliveira, C. P., Begnini, K. R., Schultze, E., Thurow, H. S., Leon, P. M., Dellagostin, O. A., Campos, V. F., Beck, R. C., Guterres, S. S., Collares, T., Pohlmann, A. R., & Seixas, F. K. (2014). Methotrexate diethyl ester-loaded lipid-core nanocapsules in aqueous solution increased antineoplastic effects in resistant breast cancer cell line. International journal of nanomedicine, 9, 1583–1591. https://doi.org/10.2147/IJN.S56506
1246. Mocan, L., Ilie, I., Matea, C., Tabaran, F., Kalman, E., Iancu, C., & Mocan, T. (2014). Surface plasmon resonance-induced photoactivation of gold nanoparticles as bactericidal agents against methicillin-resistant Staphylococcus aureus. International journal of nanomedicine, 9, 1453–1461. https://doi.org/10.2147/IJN.S54950
1247. Huang, F., You, M., Chen, T., Zhu, G., Liang, H., & Tan, W. (2014). Self-assembled hybrid nanoparticles for targeted co-delivery of two drugs into cancer cells. Chemical communications (Cambridge, England), 50(23), 3103–3105. https://doi.org/10.1039/c3cc49003c
1248. Kumari, A., Singla, R., Guliani, A., & Yadav, S. K. (2014). Nanoencapsulation for drug delivery. EXCLI journal, 13, 265–286.
1249. Wu, L., Li, X., Janagam, D. R., & Lowe, T. L. (2014). Overcoming the blood-brain barrier in chemotherapy treatment of pediatric brain tumors. Pharmaceutical research, 31(3), 531–540. https://doi.org/10.1007/s11095-013-1196-z
1250. You, J., Zhang, P., Hu, F., Du, Y., Yuan, H., Zhu, J., Wang, Z., Zhou, J., & Li, C. (2014). Near-infrared light-sensitive liposomes for the enhanced photothermal tumor treatment by the combination with chemotherapy. Pharmaceutical research, 31(3), 554–565. https://doi.org/10.1007/s11095-013-1180-7
1251. Yefimova, S. L., Kurilchenko, I. Y., Tkacheva, T. N., Kavok, N. S., Todor, I. N., Lukianova, N. Y., Chekhun, V. F., & Malyukin, Y. V. (2014). Microspectroscopic Study of Liposome-to-cell Interaction Revealed by Förster Resonance Energy Transfer. Journal of fluorescence, 24(2), 403–409. https://doi.org/10.1007/s10895-013-1305-8
1252. Chattopadhyay, S., Dash, S. K., Kar Mahapatra, S., Tripathy, S., Ghosh, T., Das, B., Das, D., Pramanik, P., & Roy, S. (2014). Chitosan-modified cobalt oxide nanoparticles stimulate TNF-α-mediated apoptosis in human leukemic cells. Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 19(3), 399–414. https://doi.org/10.1007/s00775-013-1085-2
1253. Xu, X., Sabanayagam, C. R., Harrington, D. A., Farach-Carson, M. C., & Jia, X. (2014). A hydrogel-based tumor model for the evaluation of nanoparticle-based cancer therapeutics. Biomaterials, 35(10), 3319–3330. https://doi.org/10.1016/j.biomaterials.2013.12.080
1254. Fronczyk, K., Guindani, M., Vannucci, M., Palange, A., & Decuzzi, P. (2014). A Bayesian hierarchical model for maximizing the vascular adhesion of nanoparticles. Computational mechanics, 53(3), 539–547. https://doi.org/10.1007/s00466-013-0957-1
1255. Liu, J., Ayyaswamy, P. S., Eckmann, D. M., & Radhakrishnan, R. (2014). Modelling of Binding Free Energy of Targeted Nanocarriers to Cell Surface. Heat and mass transfer = Warme- und Stoffubertragung, 50(3), 315–321. https://doi.org/10.1007/s00231-013-1274-0
1256. Abdel-Wahhab, M. A., Abdel-Wahhab, K. G., Mannaa, F. A., Hassan, N. S., Safar, R., Diab, R., Foliguet, B., Ferrari, L., & Rihn, B. H. (2014). Uptake of Eudragit Retard L (Eudragit® RL) Nanoparticles by Human THP-1 Cell Line and Its Effects on Hematology and Erythrocyte Damage in Rats. Materials (Basel, Switzerland), 7(3), 1555–1572. https://doi.org/10.3390/ma7031555
1257. Li, Y., Tong, Y., Cao, R., Tian, Z., Yang, B., & Yang, P. (2014). In vivo enhancement of anticancer therapy using bare or chemotherapeutic drug-bearing nanodiamond particles. International journal of nanomedicine, 9, 1065–1082. https://doi.org/10.2147/IJN.S54864
1258. Liu, D., Lu, K., Poon, C., & Lin, W. (2014). Metal-organic frameworks as sensory materials and imaging agents. Inorganic chemistry, 53(4), 1916–1924. https://doi.org/10.1021/ic402194c
1259. Kunjachan, S., Pola, R., Gremse, F., Theek, B., Ehling, J., Moeckel, D., Hermanns-Sachweh, B., Pechar, M., Ulbrich, K., Hennink, W. E., Storm, G., Lederle, W., Kiessling, F., & Lammers, T. (2014). Passive versus active tumor targeting using RGD- and NGR-modified polymeric nanomedicines. Nano letters, 14(2), 972–981. https://doi.org/10.1021/nl404391r
1260. Sur, S., Fries, A. C., Kinzler, K. W., Zhou, S., & Vogelstein, B. (2014). Remote loading of preencapsulated drugs into stealth liposomes. Proceedings of the National Academy of Sciences of the United States of America, 111(6), 2283–2288. https://doi.org/10.1073/pnas.1324135111
1261. Min, Y., Li, J., Liu, F., Padmanabhan, P., Yeow, E. K., & Xing, B. (2014). Recent Advance of Biological Molecular Imaging Based on Lanthanide-Doped Upconversion-Luminescent Nanomaterials. Nanomaterials (Basel, Switzerland), 4(1), 129–154. https://doi.org/10.3390/nano4010129
1262. Peer D. (2014). Harnessing RNAi nanomedicine for precision therapy. Molecular and cellular therapies, 2, 5. https://doi.org/10.1186/2052-8426-2-5
1263. Dam, D. H., Culver, K. S., & Odom, T. W. (2014). Grafting aptamers onto gold nanostars increases in vitro efficacy in a wide range of cancer cell types. Molecular pharmaceutics, 11(2), 580–587. https://doi.org/10.1021/mp4005657
1264. Bertrand, N., Wu, J., Xu, X., Kamaly, N., & Farokhzad, O. C. (2014). Cancer nanotechnology: the impact of passive and active targeting in the era of modern cancer biology. Advanced drug delivery reviews, 66, 2–25. https://doi.org/10.1016/j.addr.2013.11.009
1265. Ding, D., Tang, X., Cao, X., Wu, J., Yuan, A., Qiao, Q., Pan, J., & Hu, Y. (2014). Novel self-assembly endows human serum albumin nanoparticles with an enhanced antitumor efficacy. AAPS PharmSciTech, 15(1), 213–222. https://doi.org/10.1208/s12249-013-0041-3
1266. Hapuarachchige, S., Zhu, W., Kato, Y., & Artemov, D. (2014). Bioorthogonal, two-component delivery systems based on antibody and drug-loaded nanocarriers for enhanced internalization of nanotherapeutics. Biomaterials, 35(7), 2346–2354. https://doi.org/10.1016/j.biomaterials.2013.11.075
1267. DeWitt, M. R., Pekkanen, A. M., Robertson, J., Rylander, C. G., & Nichole Rylander, M. (2014). Influence of hyperthermia on efficacy and uptake of carbon nanohorn-cisplatin conjugates. Journal of biomechanical engineering, 136(2), 021003. https://doi.org/10.1115/1.4026318
1268. Papa, S., Ferrari, R., De Paola, M., Rossi, F., Mariani, A., Caron, I., Sammali, E., Peviani, M., Dell'Oro, V., Colombo, C., Morbidelli, M., Forloni, G., Perale, G., Moscatelli, D., & Veglianese, P. (2014). Polymeric nanoparticle system to target activated microglia/macrophages in spinal cord injury. Journal of controlled release : official journal of the Controlled Release Society, 174, 15–26. https://doi.org/10.1016/j.jconrel.2013.11.001
1269. Olcum, S., Cermak, N., Wasserman, S. C., Christine, K. S., Atsumi, H., Payer, K. R., Shen, W., Lee, J., Belcher, A. M., Bhatia, S. N., & Manalis, S. R. (2014). Weighing nanoparticles in solution at the attogram scale. Proceedings of the National Academy of Sciences of the United States of America, 111(4), 1310–1315. https://doi.org/10.1073/pnas.1318602111
1270. Kim, Y., Lobatto, M. E., Kawahara, T., Lee Chung, B., Mieszawska, A. J., Sanchez-Gaytan, B. L., Fay, F., Senders, M. L., Calcagno, C., Becraft, J., Tun Saung, M., Gordon, R. E., Stroes, E. S., Ma, M., Farokhzad, O. C., Fayad, Z. A., Mulder, W. J., & Langer, R. (2014). Probing nanoparticle translocation across the permeable endothelium in experimental atherosclerosis. Proceedings of the National Academy of Sciences of the United States of America, 111(3), 1078–1083. https://doi.org/10.1073/pnas.1322725111
1271. Sanna, V., Pala, N., & Sechi, M. (2014). Targeted therapy using nanotechnology: focus on cancer. International journal of nanomedicine, 9, 467–483. https://doi.org/10.2147/IJN.S36654
1272. Sizovs, A., Song, X., Waxham, M. N., Jia, Y., Feng, F., Chen, J., Wicker, A. C., Xu, J., Yu, Y., & Wang, J. (2014). Precisely tunable engineering of sub-30 nm monodisperse oligonucleotide nanoparticles. Journal of the American Chemical Society, 136(1), 234–240. https://doi.org/10.1021/ja408879b
1273. Srivatsan, A., Jenkins, S. V., Jeon, M., Wu, Z., Kim, C., Chen, J., & Pandey, R. K. (2014). Gold nanocage-photosensitizer conjugates for dual-modal image-guided enhanced photodynamic therapy. Theranostics, 4(2), 163–174. https://doi.org/10.7150/thno.7064
1274. Chang, C. H., Liu, S. Y., & Lee, T. W. (2014). Pharmacokinetics of BMEDA after intravenous administration in beagle dogs. Molecules (Basel, Switzerland), 19(1), 538–549. https://doi.org/10.3390/molecules19010538
1275. Stojnev, S., Krstic, M., Ristic-Petrovic, A., Stefanovic, V., & Hattori, T. (2014). Gastric cancer stem cells: therapeutic targets. Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 17(1), 13–25. https://doi.org/10.1007/s10120-013-0254-x
1276. Devulapally, R., & Paulmurugan, R. (2014). Polymer nanoparticles for drug and small silencing RNA delivery to treat cancers of different phenotypes. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 6(1), 40–60. https://doi.org/10.1002/wnan.1242
1277. Bolhassani, A., Javanzad, S., Saleh, T., Hashemi, M., Aghasadeghi, M. R., & Sadat, S. M. (2014). Polymeric nanoparticles: potent vectors for vaccine delivery targeting cancer and infectious diseases. Human vaccines & immunotherapeutics, 10(2), 321–332. https://doi.org/10.4161/hv.26796
1278. Chung, E. J., Cheng, Y., Morshed, R., Nord, K., Han, Y., Wegscheid, M. L., Auffinger, B., Wainwright, D. A., Lesniak, M. S., & Tirrell, M. V. (2014). Fibrin-binding, peptide amphiphile micelles for targeting glioblastoma. Biomaterials, 35(4), 1249–1256. https://doi.org/10.1016/j.biomaterials.2013.10.064
1279. Majumdar, D., Jung, K. H., Zhang, H., Nannapaneni, S., Wang, X., Amin, A. R., Chen, Z., Chen, Z. G., & Shin, D. M. (2014). Luteolin nanoparticle in chemoprevention: in vitro and in vivo anticancer activity. Cancer prevention research (Philadelphia, Pa.), 7(1), 65–73. https://doi.org/10.1158/1940-6207.CAPR-13-0230
1280. Cormode, D. P., Naha, P. C., & Fayad, Z. A. (2014). Nanoparticle contrast agents for computed tomography: a focus on micelles. Contrast media & molecular imaging, 9(1), 37–52. https://doi.org/10.1002/cmmi.1551
1281. Alavi, S. E., Esfahani, M. K., Ghassemi, S., Akbarzadeh, A., & Hassanshahi, G. (2014). In vitro evaluation of the efficacy of liposomal and pegylated liposomal hydroxyurea. Indian journal of clinical biochemistry : IJCB, 29(1), 84–88. https://doi.org/10.1007/s12291-013-0315-2
1282. Jin, S. E., Jin, H. E., & Hong, S. S. (2014). Targeted delivery system of nanobiomaterials in anticancer therapy: from cells to clinics. BioMed research international, 2014, 814208. https://doi.org/10.1155/2014/814208
1283. Fang, R. H., Hu, C. M., Luk, B. T., Gao, W., Copp, J. A., Tai, Y., O'Connor, D. E., & Zhang, L. (2014). Cancer cell membrane-coated nanoparticles for anticancer vaccination and drug delivery. Nano letters, 14(4), 2181–2188. https://doi.org/10.1021/nl500618u
1284. Rastogi, V., Yadav, P., Bhattacharya, S. S., Mishra, A. K., Verma, N., Verma, A., & Pandit, J. K. (2014). Carbon nanotubes: an emerging drug carrier for targeting cancer cells. Journal of drug delivery, 2014, 670815. https://doi.org/10.1155/2014/670815
1285. Makino, A., & Kimura, S. (2014). Solid tumor-targeting theranostic polymer nanoparticle in nuclear medicinal fields. TheScientificWorldJournal, 2014, 424513. https://doi.org/10.1155/2014/424513
1286. Narayanan, K., Subrahmanyam, V. M., & Venkata Rao, J. (2014). A Fractional Factorial Design to Study the Effect of Process Variables on the Preparation of Hyaluronidase Loaded PLGA Nanoparticles. Enzyme research, 2014, 162962. https://doi.org/10.1155/2014/162962
1287. Snipstad, S., Westrøm, S., Mørch, Y., Afadzi, M., Åslund, A. K., & de Lange Davies, C. (2014). Contact-mediated intracellular delivery of hydrophobic drugs from polymeric nanoparticles. Cancer nanotechnology, 5(1), 8. https://doi.org/10.1186/s12645-014-0008-4
1288. McCall, R. L., & Sirianni, R. W. (2013). PLGA nanoparticles formed by single- or double-emulsion with vitamin E-TPGS. Journal of visualized experiments : JoVE, (82), 51015. https://doi.org/10.3791/51015
1289. Anselmo, A. C., Gupta, V., Zern, B. J., Pan, D., Zakrewsky, M., Muzykantov, V., & Mitragotri, S. (2013). Delivering nanoparticles to lungs while avoiding liver and spleen through adsorption on red blood cells. ACS nano, 7(12), 11129–11137. https://doi.org/10.1021/nn404853z
1290. Valencia, P. M., Pridgen, E. M., Rhee, M., Langer, R., Farokhzad, O. C., & Karnik, R. (2013). Microfluidic platform for combinatorial synthesis and optimization of targeted nanoparticles for cancer therapy. ACS nano, 7(12), 10671–10680. https://doi.org/10.1021/nn403370e
1291. Vuković, L., Madriaga, A., Kuzmis, A., Banerjee, A., Tang, A., Tao, K., Shah, N., Král, P., & Onyuksel, H. (2013). Solubilization of therapeutic agents in micellar nanomedicines. Langmuir : the ACS journal of surfaces and colloids, 29(51), 15747–15754. https://doi.org/10.1021/la403264w
1292. Puri A. (2013). Phototriggerable liposomes: current research and future perspectives. Pharmaceutics, 6(1), 1–25. https://doi.org/10.3390/pharmaceutics6010001
1293. Wu, C., Han, D., Chen, T., Peng, L., Zhu, G., You, M., Qiu, L., Sefah, K., Zhang, X., & Tan, W. (2013). Building a multifunctional aptamer-based DNA nanoassembly for targeted cancer therapy. Journal of the American Chemical Society, 135(49), 18644–18650. https://doi.org/10.1021/ja4094617
1294. Lee, S. M., & Nguyen, S. T. (2013). Smart Nanoscale Drug Delivery Platforms from Stimuli-Responsive Polymers and Liposomes. Macromolecules, 46(23), 9169–9180. https://doi.org/10.1021/ma401529w
1295. Cheng, Q., Blais, M. O., Harris, G. M., & Jabbarzadeh, E. (2013). PLGA-carbon nanotube conjugates for intercellular delivery of caspase-3 into osteosarcoma cells. PloS one, 8(12), e81947. https://doi.org/10.1371/journal.pone.0081947
1296. Stapleton, S., Milosevic, M., Allen, C., Zheng, J., Dunne, M., Yeung, I., & Jaffray, D. A. (2013). A mathematical model of the enhanced permeability and retention effect for liposome transport in solid tumors. PloS one, 8(12), e81157. https://doi.org/10.1371/journal.pone.0081157
1297. Rizzo, L. Y., Theek, B., Storm, G., Kiessling, F., & Lammers, T. (2013). Recent progress in nanomedicine: therapeutic, diagnostic and theranostic applications. Current opinion in biotechnology, 24(6), 1159–1166. https://doi.org/10.1016/j.copbio.2013.02.020
1298. Aslan, B., Ozpolat, B., Sood, A. K., & Lopez-Berestein, G. (2013). Nanotechnology in cancer therapy. Journal of drug targeting, 21(10), 904–913. https://doi.org/10.3109/1061186X.2013.837469
1299. Gülçür, E., Thaqi, M., Khaja, F., Kuzmis, A., & Önyüksel, H. (2013). Curcumin in VIP-targeted sterically stabilized phospholipid nanomicelles: a novel therapeutic approach for breast cancer and breast cancer stem cells. Drug delivery and translational research, 3(6), 10.1007/s13346-013-0167-6. https://doi.org/10.1007/s13346-013-0167-6
1300. Zhao, Y., van Rooy, I., Hak, S., Fay, F., Tang, J., Davies, C., Skobe, M., Fisher, E. A., Radu, A., Fayad, Z. A., de Mello Donegá, C., Meijerink, A., & Mulder, W. J. (2013). Near-infrared fluorescence energy transfer imaging of nanoparticle accumulation and dissociation kinetics in tumor-bearing mice. ACS nano, 7(11), 10362–10370. https://doi.org/10.1021/nn404782p
1301. Zhang, L., & Zhao, D. (2013). Liposomal encapsulation enhances in vivo near infrared imaging of exposed phosphatidylserine in a mouse glioma model. Molecules (Basel, Switzerland), 18(12), 14613–14628. https://doi.org/10.3390/molecules181214613
1302. Viger, M. L., Sheng, W., McFearin, C. L., Berezin, M. Y., & Almutairi, A. (2013). Application of time-resolved fluorescence for direct and continuous probing of release from polymeric delivery vehicles. Journal of controlled release : official journal of the Controlled Release Society, 171(3), 308–314. https://doi.org/10.1016/j.jconrel.2013.06.018
1303. Zhu, G., Hu, R., Zhao, Z., Chen, Z., Zhang, X., & Tan, W. (2013). Noncanonical self-assembly of multifunctional DNA nanoflowers for biomedical applications. Journal of the American Chemical Society, 135(44), 16438–16445. https://doi.org/10.1021/ja406115e
1304. Wang, X., Peer, D., & Petersen, B. (2013). Molecular and Cellular Therapies: New challenges and opportunities. Molecular and cellular therapies, 1, 1. https://doi.org/10.1186/2052-8426-1-1
1305. Johnstone, T. C., Wilson, J. J., & Lippard, S. J. (2013). Monofunctional and higher-valent platinum anticancer agents. Inorganic chemistry, 52(21), 12234–12249. https://doi.org/10.1021/ic400538c
1306. Zou, P., Chen, H., Paholak, H. J., & Sun, D. (2013). Noninvasive fluorescence resonance energy transfer imaging of in vivo premature drug release from polymeric nanoparticles. Molecular pharmaceutics, 10(11), 4185–4194. https://doi.org/10.1021/mp4002393
1307. Pan, D., Kim, B., Wang, L. V., & Lanza, G. M. (2013). A brief account of nanoparticle contrast agents for photoacoustic imaging. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 5(6), 517–543. https://doi.org/10.1002/wnan.1231
1308. Oberoi, H. S., Nukolova, N. V., Kabanov, A. V., & Bronich, T. K. (2013). Nanocarriers for delivery of platinum anticancer drugs. Advanced drug delivery reviews, 65(13-14), 1667–1685. https://doi.org/10.1016/j.addr.2013.09.014
1309. Markman, J. L., Rekechenetskiy, A., Holler, E., & Ljubimova, J. Y. (2013). Nanomedicine therapeutic approaches to overcome cancer drug resistance. Advanced drug delivery reviews, 65(13-14), 1866–1879. https://doi.org/10.1016/j.addr.2013.09.019
1310. Zhao, Y., Alakhova, D. Y., & Kabanov, A. V. (2013). Can nanomedicines kill cancer stem cells?. Advanced drug delivery reviews, 65(13-14), 1763–1783. https://doi.org/10.1016/j.addr.2013.09.016
1311. Chauhan, V. P., & Jain, R. K. (2013). Strategies for advancing cancer nanomedicine. Nature materials, 12(11), 958–962. https://doi.org/10.1038/nmat3792
1312. Akinc, A., & Battaglia, G. (2013). Exploiting endocytosis for nanomedicines. Cold Spring Harbor perspectives in biology, 5(11), a016980. https://doi.org/10.1101/cshperspect.a016980
1313. Zhang, S., Mu, Y., Zhang, J. Z., & Xu, W. (2013). Effect of self-assembly of fullerene nano-particles on lipid membrane. PloS one, 8(10), e77436. https://doi.org/10.1371/journal.pone.0077436
1314. Yasunaga, M., Furuta, M., Ogata, K., Koga, Y., Yamamoto, Y., Takigahira, M., & Matsumura, Y. (2013). The significance of microscopic mass spectrometry with high resolution in the visualisation of drug distribution. Scientific reports, 3, 3050. https://doi.org/10.1038/srep03050
1315. Agarwal, R., Singh, V., Jurney, P., Shi, L., Sreenivasan, S. V., & Roy, K. (2013). Mammalian cells preferentially internalize hydrogel nanodiscs over nanorods and use shape-specific uptake mechanisms. Proceedings of the National Academy of Sciences of the United States of America, 110(43), 17247–17252. https://doi.org/10.1073/pnas.1305000110
1316. Gianella, A., Mieszawska, A. J., Hoeben, F. J., Janssen, H. M., Jarzyna, P. A., Cormode, D. P., Costa, K. D., Rao, S., Farokhzad, O. C., Langer, R., Fayad, Z. A., & Mulder, W. J. (2013). Synthesis and in vitro evaluation of a multifunctional and surface-switchable nanoemulsion platform. Chemical communications (Cambridge, England), 49(82), 9392–9394. https://doi.org/10.1039/c3cc43618g
1317. Xu, W., Burke, J. F., Pilla, S., Chen, H., Jaskula-Sztul, R., & Gong, S. (2013). Octreotide-functionalized and resveratrol-loaded unimolecular micelles for targeted neuroendocrine cancer therapy. Nanoscale, 5(20), 9924–9933. https://doi.org/10.1039/c3nr03102k
1318. Xing, H., Tang, L., Yang, X., Hwang, K., Wang, W., Yin, Q., Wong, N. Y., Dobrucki, L. W., Yasui, N., Katzenellenbogen, J. A., Helferich, W. G., Cheng, J., & Lu, Y. (2013). Selective Delivery of an Anticancer Drug with Aptamer-Functionalized Liposomes to Breast Cancer Cells in Vitro and in Vivo. Journal of materials chemistry. B, 1(39), 5288–5297. https://doi.org/10.1039/C3TB20412J
1319. Srinivasan, S., Alexander, J. F., Driessen, W. H., Leonard, F., Ye, H., Liu, X., Arap, W., Pasqualini, R., Ferrari, M., & Godin, B. (2013). Bacteriophage Associated Silicon Particles: Design and Characterization of a Novel Theranostic Vector with Improved Payload Carrying Potential. Journal of materials chemistry. B, 1(39), 10.1039/C3TB20595A. https://doi.org/10.1039/C3TB20595A
1320. Guduru, R., Liang, P., Runowicz, C., Nair, M., Atluri, V., & Khizroev, S. (2013). Magneto-electric nanoparticles to enable field-controlled high-specificity drug delivery to eradicate ovarian cancer cells. Scientific reports, 3, 2953. https://doi.org/10.1038/srep02953
1321. Liu, J., Gao, A. X., & Johnson, J. A. (2013). Particles without a box: brush-first synthesis of photodegradable PEG star polymers under ambient conditions. Journal of visualized experiments : JoVE, (80), 50874. https://doi.org/10.3791/50874
1322. Fang, R. H., Hu, C. M., Chen, K. N., Luk, B. T., Carpenter, C. W., Gao, W., Li, S., Zhang, D. E., Lu, W., & Zhang, L. (2013). Lipid-insertion enables targeting functionalization of erythrocyte membrane-cloaked nanoparticles. Nanoscale, 5(19), 8884–8888. https://doi.org/10.1039/c3nr03064d
1323. Wang, C., Wu, C., Zhou, X., Han, T., Xin, X., Wu, J., Zhang, J., & Guo, S. (2013). Enhancing cell nucleus accumulation and DNA cleavage activity of anti-cancer drug via graphene quantum dots. Scientific reports, 3, 2852. https://doi.org/10.1038/srep02852
1324. Dadgar, N., Alavi, S. E., Esfahani, M. K., & Akbarzadeh, A. (2013). Study of toxicity effect of pegylated nanoliposomal artemisinin on breast cancer cell line. Indian journal of clinical biochemistry : IJCB, 28(4), 410–412. https://doi.org/10.1007/s12291-013-0306-3
1325. Mezzaroba, N., Zorzet, S., Secco, E., Biffi, S., Tripodo, C., Calvaruso, M., Mendoza-Maldonado, R., Capolla, S., Granzotto, M., Spretz, R., Larsen, G., Noriega, S., Lucafò, M., Mansilla, E., Garrovo, C., Marín, G. H., Baj, G., Gattei, V., Pozzato, G., Núñez, L., … Macor, P. (2013). New potential therapeutic approach for the treatment of B-Cell malignancies using chlorambucil/hydroxychloroquine-loaded anti-CD20 nanoparticles. PloS one, 8(9), e74216. https://doi.org/10.1371/journal.pone.0074216
1326. Di Mascolo, D., J Lyon, C., Aryal, S., Ramirez, M. R., Wang, J., Candeloro, P., Guindani, M., Hsueh, W. A., & Decuzzi, P. (2013). Rosiglitazone-loaded nanospheres for modulating macrophage-specific inflammation in obesity. Journal of controlled release : official journal of the Controlled Release Society, 170(3), 460–468. https://doi.org/10.1016/j.jconrel.2013.06.012
1327. Mieszawska, A. J., Kim, Y., Gianella, A., van Rooy, I., Priem, B., Labarre, M. P., Ozcan, C., Cormode, D. P., Petrov, A., Langer, R., Farokhzad, O. C., Fayad, Z. A., & Mulder, W. J. (2013). Synthesis of polymer-lipid nanoparticles for image-guided delivery of dual modality therapy. Bioconjugate chemistry, 24(9), 1429–1434. https://doi.org/10.1021/bc400166j
1328. Morton, S. W., Herlihy, K. P., Shopsowitz, K. E., Deng, Z. J., Chu, K. S., Bowerman, C. J., Desimone, J. M., & Hammond, P. T. (2013). Scalable manufacture of built-to-order nanomedicine: spray-assisted layer-by-layer functionalization of PRINT nanoparticles. Advanced materials (Deerfield Beach, Fla.), 25(34), 4707–4713. https://doi.org/10.1002/adma.201302025
1329. Khushnud, T., & Mousa, S. A. (2013). Potential role of naturally derived polyphenols and their nanotechnology delivery in cancer. Molecular biotechnology, 55(1), 78–86. https://doi.org/10.1007/s12033-012-9623-7
1330. Nair K, L., Jagadeeshan, S., Nair S, A., & Kumar, G. S. (2013). Folic acid conjugated δ-valerolactone-poly(ethylene glycol) based triblock copolymer as a promising carrier for targeted doxorubicin delivery. PloS one, 8(8), e70697. https://doi.org/10.1371/journal.pone.0070697
1331. Frasconi, M., Liu, Z., Lei, J., Wu, Y., Strekalova, E., Malin, D., Ambrogio, M. W., Chen, X., Botros, Y. Y., Cryns, V. L., Sauvage, J. P., & Stoddart, J. F. (2013). Photoexpulsion of surface-grafted ruthenium complexes and subsequent release of cytotoxic cargos to cancer cells from mesoporous silica nanoparticles. Journal of the American Chemical Society, 135(31), 11603–11613. https://doi.org/10.1021/ja405058y
1332. Gullotti, E., Park, J., & Yeo, Y. (2013). Polydopamine-based surface modification for the development of peritumorally activatable nanoparticles. Pharmaceutical research, 30(8), 1956–1967. https://doi.org/10.1007/s11095-013-1039-y
1333. Lee, H. J., & Bae, Y. (2013). Brushed block copolymer micelles with pH-sensitive pendant groups for controlled drug delivery. Pharmaceutical research, 30(8), 2077–2086. https://doi.org/10.1007/s11095-013-1060-1
1334. Wojton, J., Chu, Z., Mathsyaraja, H., Meisen, W. H., Denton, N., Kwon, C. H., Chow, L. M., Palascak, M., Franco, R., Bourdeau, T., Thornton, S., Ostrowski, M. C., Kaur, B., & Qi, X. (2013). Systemic delivery of SapC-DOPS has antiangiogenic and antitumor effects against glioblastoma. Molecular therapy : the journal of the American Society of Gene Therapy, 21(8), 1517–1525. https://doi.org/10.1038/mt.2013.114
1335. Kumar, R., Kulkarni, A., Nabulsi, J., Nagesha, D. K., Cormack, R., Makrigiorgos, M. G., & Sridhar, S. (2013). Facile Synthesis of PEGylated PLGA Nanoparticles Encapsulating Doxorubicin and its In Vitro Evaluation as Potent Drug Delivery Vehicle. Drug delivery and translational research, 3(4), 299–308. https://doi.org/10.1007/s13346-012-0124-9
1336. Upreti, M., Jyoti, A., & Sethi, P. (2013). Tumor microenvironment and nanotherapeutics. Translational cancer research, 2(4), 309–319. https://doi.org/10.3978/j.issn.2218-676X.2013.08.11
1337. Qaderi, A., Dadgar, N., Mansouri, H., Alavi, S. E., Esfahani, M. K., & Akbarzadeh, A. (2013). Modeling and prediction of cytotoxicity of artemisinin for treatment of the breast cancer by using artificial neural networks. SpringerPlus, 2, 340. https://doi.org/10.1186/2193-1801-2-340
1338. Chien, M. P., Thompson, M. P., Barback, C. V., Ku, T. H., Hall, D. J., & Gianneschi, N. C. (2013). Enzyme-directed assembly of a nanoparticle probe in tumor tissue. Advanced materials (Deerfield Beach, Fla.), 25(26), 3599–3604. https://doi.org/10.1002/adma.201300823
1339. Ta, T., & Porter, T. M. (2013). Thermosensitive liposomes for localized delivery and triggered release of chemotherapy. Journal of controlled release : official journal of the Controlled Release Society, 169(1-2), 112–125. https://doi.org/10.1016/j.jconrel.2013.03.036
1340. Cabral, H., Murakami, M., Hojo, H., Terada, Y., Kano, M. R., Chung, U. I., Nishiyama, N., & Kataoka, K. (2013). Targeted therapy of spontaneous murine pancreatic tumors by polymeric micelles prolongs survival and prevents peritoneal metastasis. Proceedings of the National Academy of Sciences of the United States of America, 110(28), 11397–11402. https://doi.org/10.1073/pnas.1301348110
1341. Amoozgar, Z., Park, J., Lin, Q., Weidle, J. H., 3rd, & Yeo, Y. (2013). Development of quinic acid-conjugated nanoparticles as a drug carrier to solid tumors. Biomacromolecules, 14(7), 2389–2395. https://doi.org/10.1021/bm400512g
1342. Xu, W., Siddiqui, I. A., Nihal, M., Pilla, S., Rosenthal, K., Mukhtar, H., & Gong, S. (2013). Aptamer-conjugated and doxorubicin-loaded unimolecular micelles for targeted therapy of prostate cancer. Biomaterials, 34(21), 5244–5253. https://doi.org/10.1016/j.biomaterials.2013.03.006
1343. McRae Page, S., Martorella, M., Parelkar, S., Kosif, I., & Emrick, T. (2013). Disulfide cross-linked phosphorylcholine micelles for triggered release of camptothecin. Molecular pharmaceutics, 10(7), 2684–2692. https://doi.org/10.1021/mp400114n
1344. Alavi, S. E., Esfahani, M. K., Alavi, F., Movahedi, F., & Akbarzadeh, A. (2013). Drug delivery of hydroxyurea to breast cancer using liposomes. Indian journal of clinical biochemistry : IJCB, 28(3), 299–302. https://doi.org/10.1007/s12291-012-0291-y
1345. Sanna, V., Siddiqui, I. A., Sechi, M., & Mukhtar, H. (2013). Nanoformulation of natural products for prevention and therapy of prostate cancer. Cancer letters, 334(1), 142–151. https://doi.org/10.1016/j.canlet.2012.11.037
1346. Cui, F., Li, Y., Zhou, S., Jia, M., Yang, X., Yu, F., Ye, S., Hou, Z., & Xie, L. (2013). A comparative in vitro evaluation of self-assembled PTX-PLA and PTX-MPEG-PLA nanoparticles. Nanoscale research letters, 8(1), 301. https://doi.org/10.1186/1556-276X-8-301
1347. Tsekouras, K., Goncharenko, I., Colvin, M. E., Huang, K. C., & Gopinathan, A. (2013). Design of High-Specificity Nanocarriers by Exploiting Non-Equilibrium Effects in Cancer Cell Targeting. PloS one, 8(6), e65623. https://doi.org/10.1371/journal.pone.0065623
1348. O'Halloran, T. V., Ahn, R., Hankins, P., Swindell, E., & Mazar, A. P. (2013). The many spaces of uPAR: delivery of theranostic agents and nanobins to multiple tumor compartments through a single target. Theranostics, 3(7), 496–506. https://doi.org/10.7150/thno.4953
1349. Lee, S. M., Tsai, D. H., Hackley, V. A., Brechbiel, M. W., & Cook, R. F. (2013). Surface-engineered nanomaterials as X-ray absorbing adjuvant agents for Auger-mediated chemo-radiation. Nanoscale, 5(12), 5252–5256. https://doi.org/10.1039/c3nr00333g
1350. Zhang, Y., Yin, Q., Yin, L., Ma, L., Tang, L., & Cheng, J. (2013). Chain-shattering polymeric therapeutics with on-demand drug-release capability. Angewandte Chemie (International ed. in English), 52(25), 6435–6439. https://doi.org/10.1002/anie.201300497
1351. Sunoqrot, S., Liu, Y., Kim, D. H., & Hong, S. (2013). In vitro evaluation of dendrimer-polymer hybrid nanoparticles on their controlled cellular targeting kinetics. Molecular pharmaceutics, 10(6), 2157–2166. https://doi.org/10.1021/mp300560n
1352. Krishnan, V., Xu, X., Barwe, S. P., Yang, X., Czymmek, K., Waldman, S. A., Mason, R. W., Jia, X., & Rajasekaran, A. K. (2013). Dexamethasone-loaded block copolymer nanoparticles induce leukemia cell death and enhance therapeutic efficacy: a novel application in pediatric nanomedicine. Molecular pharmaceutics, 10(6), 2199–2210. https://doi.org/10.1021/mp300350e
1353. Severino, P., Fangueiro, J. F., Ferreira, S. V., Basso, R., Chaud, M. V., Santana, M. H., Rosmaninho, A., & Souto, E. B. (2013). Nanoemulsions and nanoparticles for non-melanoma skin cancer: effects of lipid materials. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 15(6), 417–424. https://doi.org/10.1007/s12094-012-0982-0
1354. Rosso, F., Quagliariello, V., Tortora, C., Di Lazzaro, A., Barbarisi, A., & Iaffaioli, R. V. (2013). Cross-linked hyaluronic acid sub-micron particles: in vitro and in vivo biodistribution study in cancer xenograft model. Journal of materials science. Materials in medicine, 24(6), 1473–1481. https://doi.org/10.1007/s10856-013-4895-4
1355. Tang, L., & Cheng, J. (2013). Nonporous Silica Nanoparticles for Nanomedicine Application. Nano today, 8(3), 290–312. https://doi.org/10.1016/j.nantod.2013.04.007
1356. Grama, C. N., Venkatpurwar, V. P., Lamprou, D. A., & Ravi Kumar, M. N. (2013). Towards scale-up and regulatory shelf-stability testing of curcumin encapsulated polyester nanoparticles. Drug delivery and translational research, 3(3), 286–293. https://doi.org/10.1007/s13346-013-0150-2
1357. Martinez, J. O., Parodi, A., Liu, X., Kolonin, M. G., Ferrari, M., & Tasciotti, E. (2013). Evaluation of cell function upon nanovector internalization. Small (Weinheim an der Bergstrasse, Germany), 9(9-10), 1696–1702. https://doi.org/10.1002/smll.201202001
1358. Li, J., Kuang, Y., Shi, J., Gao, Y., Zhou, J., & Xu, B. (2013). The conjugation of nonsteroidal anti-inflammatory drugs (NSAID) to small peptides for generating multifunctional supramolecular nanofibers/hydrogels. Beilstein journal of organic chemistry, 9, 908–917. https://doi.org/10.3762/bjoc.9.104
1359. Florinas, S., Nam, H. Y., & Kim, S. W. (2013). Enhanced siRNA delivery using a combination of an arginine-grafted bioreducible polymer, ultrasound, and microbubbles in cancer cells. Molecular pharmaceutics, 10(5), 2021–2030. https://doi.org/10.1021/mp400048p
1360. Doane, T., & Burda, C. (2013). Nanoparticle mediated non-covalent drug delivery. Advanced drug delivery reviews, 65(5), 607–621. https://doi.org/10.1016/j.addr.2012.05.012
1361. Valencia, P. M., Pridgen, E. M., Perea, B., Gadde, S., Sweeney, C., Kantoff, P. W., Bander, N. H., Lippard, S. J., Langer, R., Karnik, R., & Farokhzad, O. C. (2013). Synergistic cytotoxicity of irinotecan and cisplatin in dual-drug targeted polymeric nanoparticles. Nanomedicine (London, England), 8(5), 687–698. https://doi.org/10.2217/nnm.12.134
1362. Chan, C. N., Dietrich, I., Hosie, M. J., & Willett, B. J. (2013). Recent developments in human immunodeficiency virus-1 latency research. The Journal of general virology, 94(Pt 5), 917–932. https://doi.org/10.1099/vir.0.049296-0
1363. Colby, A. H., Colson, Y. L., & Grinstaff, M. W. (2013). Microscopy and tunable resistive pulse sensing characterization of the swelling of pH-responsive, polymeric expansile nanoparticles. Nanoscale, 5(8), 3496–3504. https://doi.org/10.1039/c3nr00114h
1364. Hossain, S., Yamamoto, H., Chowdhury, E. H., Wu, X., Hirose, H., Haque, A., Doki, Y., Mori, M., & Akaike, T. (2013). Fabrication and intracellular delivery of doxorubicin/carbonate apatite nanocomposites: effect on growth retardation of established colon tumor. PloS one, 8(4), e60428. https://doi.org/10.1371/journal.pone.0060428
1365. Joo, K. I., Xiao, L., Liu, S., Liu, Y., Lee, C. L., Conti, P. S., Wong, M. K., Li, Z., & Wang, P. (2013). Crosslinked multilamellar liposomes for controlled delivery of anticancer drugs. Biomaterials, 34(12), 3098–3109. https://doi.org/10.1016/j.biomaterials.2013.01.039
1366. Shi, S., Yang, K., Hong, H., Valdovinos, H. F., Nayak, T. R., Zhang, Y., Theuer, C. P., Barnhart, T. E., Liu, Z., & Cai, W. (2013). Tumor vasculature targeting and imaging in living mice with reduced graphene oxide. Biomaterials, 34(12), 3002–3009. https://doi.org/10.1016/j.biomaterials.2013.01.047
1367. Singh, A. K., Pandey, A., Tewari, M., Kumar, R., Sharma, A., Pandey, H. P., & Shukla, H. S. (2013). Prospects of nano-material in breast cancer management. Pathology oncology research : POR, 19(2), 155–165. https://doi.org/10.1007/s12253-013-9609-1
1368. Lee, J. H., Kim, J. W., & Cheon, J. (2013). Magnetic nanoparticles for multi-imaging and drug delivery. Molecules and cells, 35(4), 274–284. https://doi.org/10.1007/s10059-013-0103-0
1369. Lin, C. H., Al-Suwayeh, S. A., Hung, C. F., Chen, C. C., & Fang, J. Y. (2013). Camptothecin-Loaded Liposomes with α-Melanocyte-Stimulating Hormone Enhance Cytotoxicity Toward and Cellular Uptake by Melanomas: An Application of Nanomedicine on Natural Product. Journal of traditional and complementary medicine, 3(2), 102–109. https://doi.org/10.4103/2225-4110.110423
1370. Moore, T. L., Pitzer, J. E., Podila, R., Wang, X., Lewis, R. L., Grimes, S. W., Wilson, J. R., Skjervold, E., Brown, J. M., Rao, A., & Alexis, F. (2013). Multifunctional Polymer-Coated Carbon Nanotubes for Safe Drug Delivery. Particle & particle systems characterization : measurement and description of particle properties and behavior in powders and other disperse systems, 30(4), 365–373. https://doi.org/10.1002/ppsc.201200145
1371. Panzarini, E., Inguscio, V., Tenuzzo, B. A., Carata, E., & Dini, L. (2013). Nanomaterials and autophagy: new insights in cancer treatment. Cancers, 5(1), 296–319. https://doi.org/10.3390/cancers5010296
1372. Kim, S. T., Saha, K., Kim, C., & Rotello, V. M. (2013). The role of surface functionality in determining nanoparticle cytotoxicity. Accounts of chemical research, 46(3), 681–691. https://doi.org/10.1021/ar3000647
1373. Yin, Q., Tong, R., Xu, Y., Baek, K., Dobrucki, L. W., Fan, T. M., & Cheng, J. (2013). Drug-initiated ring-opening polymerization of O-carboxyanhydrides for the preparation of anticancer drug-poly(O-carboxyanhydride) nanoconjugates. Biomacromolecules, 14(3), 920–929. https://doi.org/10.1021/bm301999c
1374. Gormley, A. J., Larson, N., Banisadr, A., Robinson, R., Frazier, N., Ray, A., & Ghandehari, H. (2013). Plasmonic photothermal therapy increases the tumor mass penetration of HPMA copolymers. Journal of controlled release : official journal of the Controlled Release Society, 166(2), 130–138. https://doi.org/10.1016/j.jconrel.2012.12.007
1375. Fan, Z., Senapati, D., Singh, A. K., & Ray, P. C. (2013). Theranostic magnetic core-plasmonic shell star shape nanoparticle for the isolation of targeted rare tumor cells from whole blood, fluorescence imaging, and photothermal destruction of cancer. Molecular pharmaceutics, 10(3), 857–866. https://doi.org/10.1021/mp300468q
1376. Pusic, K., Aguilar, Z., McLoughlin, J., Kobuch, S., Xu, H., Tsang, M., Wang, A., & Hui, G. (2013). Iron oxide nanoparticles as a clinically acceptable delivery platform for a recombinant blood-stage human malaria vaccine. FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 27(3), 1153–1166. https://doi.org/10.1096/fj.12-218362
1377. Hossain, S. S., Zhang, Y., Liang, X., Hussain, F., Ferrari, M., Hughes, T. J., & Decuzzi, P. (2013). In silico vascular modeling for personalized nanoparticle delivery. Nanomedicine (London, England), 8(3), 343–357. https://doi.org/10.2217/nnm.12.124
1378. Alexiou C. (2013). Nanomedizin. Innovative anwendungen in der medizin [Nanomedicine. Innovative applications in medicine]. HNO, 61(3), 197–201. https://doi.org/10.1007/s00106-012-2562-6
1379. Gonzalez, L., Loza, R. J., Han, K. Y., Sunoqrot, S., Cunningham, C., Purta, P., Drake, J., Jain, S., Hong, S., & Chang, J. H. (2013). Nanotechnology in corneal neovascularization therapy--a review. Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics, 29(2), 124–134. https://doi.org/10.1089/jop.2012.0158
1380. Auffinger, B., Morshed, R., Tobias, A., Cheng, Y., Ahmed, A. U., & Lesniak, M. S. (2013). Drug-loaded nanoparticle systems and adult stem cells: a potential marriage for the treatment of malignant glioma?. Oncotarget, 4(3), 378–396. https://doi.org/10.18632/oncotarget.937
1381. Cheetham, A. G., Zhang, P., Lin, Y. A., Lock, L. L., & Cui, H. (2013). Supramolecular nanostructures formed by anticancer drug assembly. Journal of the American Chemical Society, 135(8), 2907–2910. https://doi.org/10.1021/ja3115983
1382. Salvador-Morales, C., Valencia, P. M., Gao, W., Karnik, R., & Farokhzad, O. C. (2013). Spontaneous formation of heterogeneous patches on polymer-lipid core-shell particle surfaces during self-assembly. Small (Weinheim an der Bergstrasse, Germany), 9(4), 511–517. https://doi.org/10.1002/smll.201201499
1383. Mashaghi, S., Jadidi, T., Koenderink, G., & Mashaghi, A. (2013). Lipid nanotechnology. International journal of molecular sciences, 14(2), 4242–4282. https://doi.org/10.3390/ijms14024242
1384. Ayyaswamy, P. S., Muzykantov, V., Eckmann, D. M., & Radhakrishnan, R. (2013). Nanocarrier Hydrodynamics and Binding in Targeted Drug Delivery: Challenges in Numerical Modeling and Experimental Validation. Journal of nanotechnology in engineering and medicine, 4(1), 101011–1010115. https://doi.org/10.1115/1.4024004
1385. Sano, K., Nakajima, T., Choyke, P. L., & Kobayashi, H. (2013). Markedly enhanced permeability and retention effects induced by photo-immunotherapy of tumors. ACS nano, 7(1), 717–724. https://doi.org/10.1021/nn305011p
1386. Pearson, R. M., Patra, N., Hsu, H. J., Uddin, S., Král, P., & Hong, S. (2013). Positively Charged Dendron Micelles Display Negligible Cellular Interactions. ACS macro letters, 2(1), 77–81. https://doi.org/10.1021/mz300533w
1387. Yang, J., Srinivasan, A., Sun, Y., Mrazek, J., Shu, Z., Kickhoefer, V. A., & Rome, L. H. (2013). Vault nanoparticles engineered with the protein transduction domain, TAT48, enhances cellular uptake. Integrative biology : quantitative biosciences from nano to macro, 5(1), 151–158. https://doi.org/10.1039/c2ib20119d
1388. Black, K. C., Yi, J., Rivera, J. G., Zelasko-Leon, D. C., & Messersmith, P. B. (2013). Polydopamine-enabled surface functionalization of gold nanorods for cancer cell-targeted imaging and photothermal therapy. Nanomedicine (London, England), 8(1), 17–28. https://doi.org/10.2217/nnm.12.82
1389. Koshkaryev, A., Sawant, R., Deshpande, M., & Torchilin, V. (2013). Immunoconjugates and long circulating systems: origins, current state of the art and future directions. Advanced drug delivery reviews, 65(1), 24–35. https://doi.org/10.1016/j.addr.2012.08.009
1390. MacEwan, S. R., & Chilkoti, A. (2013). Harnessing the power of cell-penetrating peptides: activatable carriers for targeting systemic delivery of cancer therapeutics and imaging agents. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 5(1), 31–48. https://doi.org/10.1002/wnan.1197
1391. Lee, S. Y., Kim, S., Tyler, J. Y., Park, K., & Cheng, J. X. (2013). Blood-stable, tumor-adaptable disulfide bonded mPEG-(Cys)4-PDLLA micelles for chemotherapy. Biomaterials, 34(2), 552–561. https://doi.org/10.1016/j.biomaterials.2012.09.065
1392. Kaur, R., & Badea, I. (2013). Nanodiamonds as novel nanomaterials for biomedical applications: drug delivery and imaging systems. International journal of nanomedicine, 8, 203–220. https://doi.org/10.2147/IJN.S37348
1393. Shao, J., Griffin, R. J., Galanzha, E. I., Kim, J. W., Koonce, N., Webber, J., Mustafa, T., Biris, A. S., Nedosekin, D. A., & Zharov, V. P. (2013). Photothermal nanodrugs: potential of TNF-gold nanospheres for cancer theranostics. Scientific reports, 3, 1293. https://doi.org/10.1038/srep01293
1394. Sah, H., Thoma, L. A., Desu, H. R., Sah, E., & Wood, G. C. (2013). Concepts and practices used to develop functional PLGA-based nanoparticulate systems. International journal of nanomedicine, 8, 747–765. https://doi.org/10.2147/IJN.S40579
1395. Frieboes, H. B., Wu, M., Lowengrub, J., Decuzzi, P., & Cristini, V. (2013). A computational model for predicting nanoparticle accumulation in tumor vasculature. PloS one, 8(2), e56876. https://doi.org/10.1371/journal.pone.0056876
1396. Perche, F., & Torchilin, V. P. (2013). Recent trends in multifunctional liposomal nanocarriers for enhanced tumor targeting. Journal of drug delivery, 2013, 705265. https://doi.org/10.1155/2013/705265
1397. Yang, C., Wang, J., Chen, D., Chen, J., Xiong, F., Zhang, H., Zhang, Y., Gu, N., & Dou, J. (2013). Paclitaxel-Fe3O4 nanoparticles inhibit growth of CD138(-) CD34(-) tumor stem-like cells in multiple myeloma-bearing mice. International journal of nanomedicine, 8, 1439–1449. https://doi.org/10.2147/IJN.S38447
1398. Shi, J., Wang, Z., Wang, L., Wang, H., Li, L., Yu, X., Zhang, J., Ma, R., & Zhang, Z. (2013). Photodynamic therapy of a 2-methoxyestradiol tumor-targeting drug delivery system mediated by Asn-Gly-Arg in breast cancer. International journal of nanomedicine, 8, 1551–1562. https://doi.org/10.2147/IJN.S40011
1399. Bahmani, B., Lytle, C. Y., Walker, A. M., Gupta, S., Vullev, V. I., & Anvari, B. (2013). Effects of nanoencapsulation and PEGylation on biodistribution of indocyanine green in healthy mice: quantitative fluorescence imaging and analysis of organs. International journal of nanomedicine, 8, 1609–1620. https://doi.org/10.2147/IJN.S42511
1400. Bao, G., Mitragotri, S., & Tong, S. (2013). Multifunctional nanoparticles for drug delivery and molecular imaging. Annual review of biomedical engineering, 15, 253–282. https://doi.org/10.1146/annurev-bioeng-071812-152409
1401. Zhou, J., Shum, K. T., Burnett, J. C., & Rossi, J. J. (2013). Nanoparticle-Based Delivery of RNAi Therapeutics: Progress and Challenges. Pharmaceuticals (Basel, Switzerland), 6(1), 85–107. https://doi.org/10.3390/ph6010085
1402. Liu, Y., Ji, M., Wong, M. K., Joo, K. I., & Wang, P. (2013). Enhanced therapeutic efficacy of iRGD-conjugated crosslinked multilayer liposomes for drug delivery. BioMed research international, 2013, 378380. https://doi.org/10.1155/2013/378380
1403. Qin, L., Wang, M., Zhu, R., You, S., Zhou, P., & Wang, S. (2013). The in vitro sustained release profile and antitumor effect of etoposide-layered double hydroxide nanohybrids. International journal of nanomedicine, 8, 2053–2064. https://doi.org/10.2147/IJN.S43203
1404. Bhosale, S. V., & Bhosale, S. V. (2013). Yoctowells as a simple model system for the encapsulation and controlled release of bioactive molecules. Scientific reports, 3, 1982. https://doi.org/10.1038/srep01982
1405. Li, J. M., Wang, Y. Y., Zhang, W., Su, H., Ji, L. N., & Mao, Z. W. (2013). Low-weight polyethylenimine cross-linked 2-hydroxypopyl-β-cyclodextrin and folic acid as an efficient and nontoxic siRNA carrier for gene silencing and tumor inhibition by VEGF siRNA. International journal of nanomedicine, 8, 2101–2117. https://doi.org/10.2147/IJN.S42440
1406. Lee, T. R., Choi, M., Kopacz, A. M., Yun, S. H., Liu, W. K., & Decuzzi, P. (2013). On the near-wall accumulation of injectable particles in the microcirculation: smaller is not better. Scientific reports, 3, 2079. https://doi.org/10.1038/srep02079
1407. Scherzinger-Laude, K., Schönherr, C., Lewrick, F., Süss, R., Francese, G., & Rössler, J. (2013). Treatment of neuroblastoma and rhabdomyosarcoma using RGD-modified liposomal formulations of patupilone (EPO906). International journal of nanomedicine, 8, 2197–2211. https://doi.org/10.2147/IJN.S44025
1408. Shi, J., Ma, R., Wang, L., Zhang, J., Liu, R., Li, L., Liu, Y., Hou, L., Yu, X., Gao, J., & Zhang, Z. (2013). The application of hyaluronic acid-derivatized carbon nanotubes in hematoporphyrin monomethyl ether-based photodynamic therapy for in vivo and in vitro cancer treatment. International journal of nanomedicine, 8, 2361–2373. https://doi.org/10.2147/IJN.S45407
1409. Bahmani, B., Bacon, D., & Anvari, B. (2013). Erythrocyte-derived photo-theranostic agents: hybrid nano-vesicles containing indocyanine green for near infrared imaging and therapeutic applications. Scientific reports, 3, 2180. https://doi.org/10.1038/srep02180
1410. Jeyamohan, P., Hasumura, T., Nagaoka, Y., Yoshida, Y., Maekawa, T., & Kumar, D. S. (2013). Accelerated killing of cancer cells using a multifunctional single-walled carbon nanotube-based system for targeted drug delivery in combination with photothermal therapy. International journal of nanomedicine, 8, 2653–2667. https://doi.org/10.2147/IJN.S46054
1411. Gu, L., Hall, D. J., Qin, Z., Anglin, E., Joo, J., Mooney, D. J., Howell, S. B., & Sailor, M. J. (2013). In vivo time-gated fluorescence imaging with biodegradable luminescent porous silicon nanoparticles. Nature communications, 4, 2326. https://doi.org/10.1038/ncomms3326
1412. Miller A. D. (2013). Lipid-based nanoparticles in cancer diagnosis and therapy. Journal of drug delivery, 2013, 165981. https://doi.org/10.1155/2013/165981
1413. Yang, S., Chen, Y., Gu, K., Dash, A., Sayre, C. L., Davies, N. M., & Ho, E. A. (2013). Novel intravaginal nanomedicine for the targeted delivery of saquinavir to CD4+ immune cells. International journal of nanomedicine, 8, 2847–2858. https://doi.org/10.2147/IJN.S46958
1414. Reshetov, V., Lassalle, H. P., François, A., Dumas, D., Hupont, S., Gräfe, S., Filipe, V., Jiskoot, W., Guillemin, F., Zorin, V., & Bezdetnaya, L. (2013). Photodynamic therapy with conventional and PEGylated liposomal formulations of mTHPC (temoporfin): comparison of treatment efficacy and distribution characteristics in vivo. International journal of nanomedicine, 8, 3817–3831. https://doi.org/10.2147/IJN.S51002
1415. Ding, W., & Guo, L. (2013). Immobilized transferrin Fe3O4@SiO2 nanoparticle with high doxorubicin loading for dual-targeted tumor drug delivery. International journal of nanomedicine, 8, 4631–4639. https://doi.org/10.2147/IJN.S51745
1416. Valetti, S., Mura, S., Stella, B., & Couvreur, P. (2013). Rational design for multifunctional non-liposomal lipid-based nanocarriers for cancer management: theory to practice. Journal of nanobiotechnology, 11 Suppl 1(Suppl 1), S6. https://doi.org/10.1186/1477-3155-11-S1-S6
1417. Lock, L. L., LaComb, M., Schwarz, K., Cheetham, A. G., Lin, Y. A., Zhang, P., & Cui, H. (2013). Self-assembly of natural and synthetic drug amphiphiles into discrete supramolecular nanostructures. Faraday discussions, 166, 285–301. https://doi.org/10.1039/c3fd00099k
1418. Podila, R., Chen, R., Ke, P. C., Brown, J. M., & Rao, A. M. (2012). Effects of surface functional groups on the formation of nanoparticle-protein corona. Applied physics letters, 101(26), 263701. https://doi.org/10.1063/1.4772509
1419. Tang, L., Yang, X., Dobrucki, L. W., Chaudhury, I., Yin, Q., Yao, C., Lezmi, S., Helferich, W. G., Fan, T. M., & Cheng, J. (2012). Aptamer-functionalized, ultra-small, monodisperse silica nanoconjugates for targeted dual-modal imaging of lymph nodes with metastatic tumors. Angewandte Chemie (International ed. in English), 51(51), 12721–12726. https://doi.org/10.1002/anie.201205271
1420. Ko, E., Kamkaew, A., & Burgess, K. (2012). Small Molecule Ligands For Active Targeting Of TrkC-expressing Tumor Cells. ACS medicinal chemistry letters, 3(12), 1008–1012. https://doi.org/10.1021/ml300227d
1421. Chen, N. T., Cheng, S. H., Liu, C. P., Souris, J. S., Chen, C. T., Mou, C. Y., & Lo, L. W. (2012). Recent advances in nanoparticle-based Förster resonance energy transfer for biosensing, molecular imaging and drug release profiling. International journal of molecular sciences, 13(12), 16598–16623. https://doi.org/10.3390/ijms131216598
1422. Bickerton, S., Jiwpanich, S., & Thayumanavan, S. (2012). Interconnected roles of scaffold hydrophobicity, drug loading, and encapsulation stability in polymeric nanocarriers. Molecular pharmaceutics, 9(12), 3569–3578. https://doi.org/10.1021/mp3004226
1423. Yang, R., Zhang, S., Kong, D., Gao, X., Zhao, Y., & Wang, Z. (2012). Biodegradable polymer-curcumin conjugate micelles enhance the loading and delivery of low-potency curcumin. Pharmaceutical research, 29(12), 3512–3525. https://doi.org/10.1007/s11095-012-0848-8
1424. Gao, W., & Zhang, L. (2012). Anticancer agents: Unleash the forces within. Nature chemistry, 4(12), 971–972. https://doi.org/10.1038/nchem.1515
1425. Nichols, J. W., & Bae, Y. H. (2012). Odyssey of a cancer nanoparticle: from injection site to site of action. Nano today, 7(6), 606–618. https://doi.org/10.1016/j.nantod.2012.10.010
1426. Ramishetti, S., & Huang, L. (2012). Intelligent design of multifunctional lipid-coated nanoparticle platforms for cancer therapy. Therapeutic delivery, 3(12), 1429–1445. https://doi.org/10.4155/tde.12.127
1427. Tong, R., Gabrielson, N. P., Fan, T. M., & Cheng, J. (2012). Polymeric Nanomedicines Based on Poly(lactide) and Poly(lactide-co-glycolide). Current opinion in solid state & materials science, 16(6), 323–332. https://doi.org/10.1016/j.cossms.2013.01.001
1428. Oliveira, M. F., Guimarães, P. P., Gomes, A. D., Suárez, D., & Sinisterra, R. D. (2012). Strategies to target tumors using nanodelivery systems based on biodegradable polymers, aspects of intellectual property, and market. Journal of chemical biology, 6(1), 7–23. https://doi.org/10.1007/s12154-012-0086-x
1429. Xiao, Y., Jaskula-Sztul, R., Javadi, A., Xu, W., Eide, J., Dammalapati, A., Kunnimalaiyaan, M., Chen, H., & Gong, S. (2012). Co-delivery of doxorubicin and siRNA using octreotide-conjugated gold nanorods for targeted neuroendocrine cancer therapy. Nanoscale, 4(22), 7185–7193. https://doi.org/10.1039/c2nr31853a
1430. Cheng, Z., Al Zaki, A., Hui, J. Z., Muzykantov, V. R., & Tsourkas, A. (2012). Multifunctional nanoparticles: cost versus benefit of adding targeting and imaging capabilities. Science (New York, N.Y.), 338(6109), 903–910. https://doi.org/10.1126/science.1226338
1431. Wu, C. H., Cao, C., Kim, J. H., Hsu, C. H., Wanebo, H. J., Bowen, W. D., Xu, J., & Marshall, J. (2012). Trojan-horse nanotube on-command intracellular drug delivery. Nano letters, 12(11), 5475–5480. https://doi.org/10.1021/nl301865c
1432. Kumar, M., Habel, J. E., Shen, Y. X., Meier, W. P., & Walz, T. (2012). High-density reconstitution of functional water channels into vesicular and planar block copolymer membranes. Journal of the American Chemical Society, 134(45), 18631–18637. https://doi.org/10.1021/ja304721r
1433. Ryvolova, M., Chomoucka, J., Drbohlavova, J., Kopel, P., Babula, P., Hynek, D., Adam, V., Eckschlager, T., Hubalek, J., Stiborova, M., Kaiser, J., & Kizek, R. (2012). Modern micro and nanoparticle-based imaging techniques. Sensors (Basel, Switzerland), 12(11), 14792–14820. https://doi.org/10.3390/s121114792
1434. Choi, K. Y., Saravanakumar, G., Park, J. H., & Park, K. (2012). Hyaluronic acid-based nanocarriers for intracellular targeting: interfacial interactions with proteins in cancer. Colloids and surfaces. B, Biointerfaces, 99, 82–94. https://doi.org/10.1016/j.colsurfb.2011.10.029
1435. Zhu, R., Cheng, K. W., Mackenzie, G., Huang, L., Sun, Y., Xie, G., Vrankova, K., Constantinides, P. P., & Rigas, B. (2012). Phospho-sulindac (OXT-328) inhibits the growth of human lung cancer xenografts in mice: enhanced efficacy and mitochondria targeting by its formulation in solid lipid nanoparticles. Pharmaceutical research, 29(11), 3090–3101. https://doi.org/10.1007/s11095-012-0801-x
1436. Dam, D. H., Culver, K. S., Sisco, P. N., & Odom, T. W. (2012). Shining light on nuclear-targeted therapy using gold nanostar constructs. Therapeutic delivery, 3(11), 1263–1267. https://doi.org/10.4155/tde.12.107
1437. Godin, B., Chiappini, C., Srinivasan, S., Alexander, J. F., Yokoi, K., Ferrari, M., Decuzzi, P., & Liu, X. (2012). Discoidal Porous Silicon Particles: Fabrication and Biodistribution in Breast Cancer Bearing Mice. Advanced functional materials, 22(20), 4225–4235. https://doi.org/10.1002/adfm.201200869
1438. Marrache, S., & Dhar, S. (2012). Engineering of blended nanoparticle platform for delivery of mitochondria-acting therapeutics. Proceedings of the National Academy of Sciences of the United States of America, 109(40), 16288–16293. https://doi.org/10.1073/pnas.1210096109
1439. Tichauer, K. M., Samkoe, K. S., Sexton, K. J., Hextrum, S. K., Yang, H. H., Klubben, W. S., Gunn, J. R., Hasan, T., & Pogue, B. W. (2012). In vivo quantification of tumor receptor binding potential with dual-reporter molecular imaging. Molecular imaging and biology, 14(5), 584–592. https://doi.org/10.1007/s11307-011-0534-y
1440. Zhang, X. Q., Xu, X., Bertrand, N., Pridgen, E., Swami, A., & Farokhzad, O. C. (2012). Interactions of nanomaterials and biological systems: Implications to personalized nanomedicine. Advanced drug delivery reviews, 64(13), 1363–1384. https://doi.org/10.1016/j.addr.2012.08.005
1441. Liu S. (2012). Epigenetics advancing personalized nanomedicine in cancer therapy. Advanced drug delivery reviews, 64(13), 1532–1543. https://doi.org/10.1016/j.addr.2012.08.004
1442. Pattani, V. P., & Tunnell, J. W. (2012). Nanoparticle-mediated photothermal therapy: a comparative study of heating for different particle types. Lasers in surgery and medicine, 44(8), 675–684. https://doi.org/10.1002/lsm.22072
1443. Valencia, P. M., Farokhzad, O. C., Karnik, R., & Langer, R. (2012). Microfluidic technologies for accelerating the clinical translation of nanoparticles. Nature nanotechnology, 7(10), 623–629. https://doi.org/10.1038/nnano.2012.168
1444. Toft, D. J., Moyer, T. J., Standley, S. M., Ruff, Y., Ugolkov, A., Stupp, S. I., & Cryns, V. L. (2012). Coassembled cytotoxic and pegylated peptide amphiphiles form filamentous nanostructures with potent antitumor activity in models of breast cancer. ACS nano, 6(9), 7956–7965. https://doi.org/10.1021/nn302503s
1445. Varela, J. A., Bexiga, M. G., Åberg, C., Simpson, J. C., & Dawson, K. A. (2012). Quantifying size-dependent interactions between fluorescently labeled polystyrene nanoparticles and mammalian cells. Journal of nanobiotechnology, 10, 39. https://doi.org/10.1186/1477-3155-10-39
1446. Nanaware-Kharade, N., Gonzalez, G. A., 3rd, Lay, J. O., Jr, Hendrickson, H. P., & Peterson, E. C. (2012). Therapeutic anti-methamphetamine antibody fragment-nanoparticle conjugates: synthesis and in vitro characterization. Bioconjugate chemistry, 23(9), 1864–1872. https://doi.org/10.1021/bc300204n
1447. Zhu, Z. J., Posati, T., Moyano, D. F., Tang, R., Yan, B., Vachet, R. W., & Rotello, V. M. (2012). The interplay of monolayer structure and serum protein interactions on the cellular uptake of gold nanoparticles. Small (Weinheim an der Bergstrasse, Germany), 8(17), 2659–2663. https://doi.org/10.1002/smll.201200794
1448. Fang, C., Kievit, F. M., Veiseh, O., Stephen, Z. R., Wang, T., Lee, D., Ellenbogen, R. G., & Zhang, M. (2012). Fabrication of magnetic nanoparticles with controllable drug loading and release through a simple assembly approach. Journal of controlled release : official journal of the Controlled Release Society, 162(1), 233–241. https://doi.org/10.1016/j.jconrel.2012.06.028
1449. Ren, D., Dalmau, M., Randall, A., Shindel, M. M., Baldi, P., & Wang, S. W. (2012). Biomimetic Design of Protein Nanomaterials for Hydrophobic Molecular Transport. Advanced functional materials, 22(15), 3170–3180. https://doi.org/10.1002/adfm.201200052
1450. Gu, L., Ruff, L. E., Qin, Z., Corr, M., Hedrick, S. M., & Sailor, M. J. (2012). Multivalent porous silicon nanoparticles enhance the immune activation potency of agonistic CD40 antibody. Advanced materials (Deerfield Beach, Fla.), 24(29), 3981–3987. https://doi.org/10.1002/adma.201200776
1451. Adriani, G., de Tullio, M. D., Ferrari, M., Hussain, F., Pascazio, G., Liu, X., & Decuzzi, P. (2012). The preferential targeting of the diseased microvasculature by disk-like particles. Biomaterials, 33(22), 5504–5513. https://doi.org/10.1016/j.biomaterials.2012.04.027
1452. Wang, Z., Liu, H., Yang, S. H., Wang, T., Liu, C., & Cao, Y. C. (2012). Nanoparticle-based artificial RNA silencing machinery for antiviral therapy. Proceedings of the National Academy of Sciences of the United States of America, 109(31), 12387–12392. https://doi.org/10.1073/pnas.1207766109
1453. Loverde, S. M., Klein, M. L., & Discher, D. E. (2012). Nanoparticle shape improves delivery: rational coarse grain molecular dynamics (rCG-MD) of taxol in worm-like PEG-PCL micelles. Advanced materials (Deerfield Beach, Fla.), 24(28), 3823–3830. https://doi.org/10.1002/adma.201103192
1454. Lukianova-Hleb, E. Y., Ren, X., Zasadzinski, J. A., Wu, X., & Lapotko, D. O. (2012). Plasmonic nanobubbles enhance efficacy and selectivity of chemotherapy against drug-resistant cancer cells. Advanced materials (Deerfield Beach, Fla.), 24(28), 3831–3837. https://doi.org/10.1002/adma.201103550
1455. Sailor, M. J., & Park, J. H. (2012). Hybrid nanoparticles for detection and treatment of cancer. Advanced materials (Deerfield Beach, Fla.), 24(28), 3779–3802. https://doi.org/10.1002/adma.201200653
1456. Mu, Q., Hondow, N. S., Krzemiński, L., Brown, A. P., Jeuken, L. J., & Routledge, M. N. (2012). Mechanism of cellular uptake of genotoxic silica nanoparticles. Particle and fibre toxicology, 9, 29. https://doi.org/10.1186/1743-8977-9-29
1457. Yuan, H., Fales, A. M., & Vo-Dinh, T. (2012). TAT peptide-functionalized gold nanostars: enhanced intracellular delivery and efficient NIR photothermal therapy using ultralow irradiance. Journal of the American Chemical Society, 134(28), 11358–11361. https://doi.org/10.1021/ja304180y
1458. de Barros, A. B., Tsourkas, A., Saboury, B., Cardoso, V. N., & Alavi, A. (2012). Emerging role of radiolabeled nanoparticles as an effective diagnostic technique. EJNMMI research, 2(1), 39. https://doi.org/10.1186/2191-219X-2-39
1459. Smith, B. R., Kempen, P., Bouley, D., Xu, A., Liu, Z., Melosh, N., Dai, H., Sinclair, R., & Gambhir, S. S. (2012). Shape matters: intravital microscopy reveals surprising geometrical dependence for nanoparticles in tumor models of extravasation. Nano letters, 12(7), 3369–3377. https://doi.org/10.1021/nl204175t
1460. Wei, X., Wang, Y., Zeng, W., Huang, F., Qin, L., Zhang, C., & Liang, W. (2012). Stability influences the biodistribution, toxicity, and anti-tumor activity of doxorubicin encapsulated in PEG-PE micelles in mice. Pharmaceutical research, 29(7), 1977–1989. https://doi.org/10.1007/s11095-012-0725-5
1461. Emoto, S., Yamaguchi, H., Kishikawa, J., Yamashita, H., Ishigami, H., & Kitayama, J. (2012). Antitumor effect and pharmacokinetics of intraperitoneal NK105, a nanomicellar paclitaxel formulation for peritoneal dissemination. Cancer science, 103(7), 1304–1310. https://doi.org/10.1111/j.1349-7006.2012.02274.x
1462. Kim, W., Brady, C., & Chaikof, E. L. (2012). Amphiphilic protein micelles for targeted in vivo imaging. Acta biomaterialia, 8(7), 2476–2482. https://doi.org/10.1016/j.actbio.2012.04.011
1463. Lukianova-Hleb, E. Y., Wagner, D. S., Brenner, M. K., & Lapotko, D. O. (2012). Cell-specific transmembrane injection of molecular cargo with gold nanoparticle-generated transient plasmonic nanobubbles. Biomaterials, 33(21), 5441–5450. https://doi.org/10.1016/j.biomaterials.2012.03.077
1464. Nduom, E. K., Bouras, A., Kaluzova, M., & Hadjipanayis, C. G. (2012). Nanotechnology applications for glioblastoma. Neurosurgery clinics of North America, 23(3), 439–449. https://doi.org/10.1016/j.nec.2012.04.006
1465. Babar, I. A., Cheng, C. J., Booth, C. J., Liang, X., Weidhaas, J. B., Saltzman, W. M., & Slack, F. J. (2012). Nanoparticle-based therapy in an in vivo microRNA-155 (miR-155)-dependent mouse model of lymphoma. Proceedings of the National Academy of Sciences of the United States of America, 109(26), E1695–E1704. https://doi.org/10.1073/pnas.1201516109
1466. Macewan, S. R., & Chilkoti, A. (2012). Digital switching of local arginine density in a genetically encoded self-assembled polypeptide nanoparticle controls cellular uptake. Nano letters, 12(6), 3322–3328. https://doi.org/10.1021/nl301529p
1467. Zhao, Y., Duan, S., Zeng, X., Liu, C., Davies, N. M., Li, B., & Forrest, M. L. (2012). Prodrug strategy for PSMA-targeted delivery of TGX-221 to prostate cancer cells. Molecular pharmaceutics, 9(6), 1705–1716. https://doi.org/10.1021/mp3000309
1468. Lee, H., Lytton-Jean, A. K., Chen, Y., Love, K. T., Park, A. I., Karagiannis, E. D., Sehgal, A., Querbes, W., Zurenko, C. S., Jayaraman, M., Peng, C. G., Charisse, K., Borodovsky, A., Manoharan, M., Donahoe, J. S., Truelove, J., Nahrendorf, M., Langer, R., & Anderson, D. G. (2012). Molecularly self-assembled nucleic acid nanoparticles for targeted in vivo siRNA delivery. Nature nanotechnology, 7(6), 389–393. https://doi.org/10.1038/nnano.2012.73
1469. Nie, T., Wong, C. C., Alston, N., Aro, P., Constantinides, P. P., & Rigas, B. (2012). Phospho-ibuprofen (MDC-917) incorporated in nanocarriers: anti-cancer activity in vitro and in vivo. British journal of pharmacology, 166(3), 991–1001. https://doi.org/10.1111/j.1476-5381.2011.01799.x
1470. Chang, J., Paillard, A., Passirani, C., Morille, M., Benoit, J. P., Betbeder, D., & Garcion, E. (2012). Transferrin adsorption onto PLGA nanoparticles governs their interaction with biological systems from blood circulation to brain cancer cells. Pharmaceutical research, 29(6), 1495–1505. https://doi.org/10.1007/s11095-011-0624-1
1471. Gormley, A. J., Larson, N., Sadekar, S., Robinson, R., Ray, A., & Ghandehari, H. (2012). Guided Delivery of Polymer Therapeutics Using Plasmonic Photothermal Therapy. Nano today, 7(3), 158–167. https://doi.org/10.1016/j.nantod.2012.04.002
1472. Radovic-Moreno, A. F., Lu, T. K., Puscasu, V. A., Yoon, C. J., Langer, R., & Farokhzad, O. C. (2012). Surface charge-switching polymeric nanoparticles for bacterial cell wall-targeted delivery of antibiotics. ACS nano, 6(5), 4279–4287. https://doi.org/10.1021/nn3008383
1473. Graf, N., Bielenberg, D. R., Kolishetti, N., Muus, C., Banyard, J., Farokhzad, O. C., & Lippard, S. J. (2012). α(V)β(3) integrin-targeted PLGA-PEG nanoparticles for enhanced anti-tumor efficacy of a Pt(IV) prodrug. ACS nano, 6(5), 4530–4539. https://doi.org/10.1021/nn301148e
1474. Hassouneh, W., Fischer, K., MacEwan, S. R., Branscheid, R., Fu, C. L., Liu, R., Schmidt, M., & Chilkoti, A. (2012). Unexpected multivalent display of proteins by temperature triggered self-assembly of elastin-like polypeptide block copolymers. Biomacromolecules, 13(5), 1598–1605. https://doi.org/10.1021/bm300321n
1475. Ryu, J. H., Bickerton, S., Zhuang, J., & Thayumanavan, S. (2012). Ligand-decorated nanogels: fast one-pot synthesis and cellular targeting. Biomacromolecules, 13(5), 1515–1522. https://doi.org/10.1021/bm300201x
1476. McDaniel, J. R., Macewan, S. R., Dewhirst, M., & Chilkoti, A. (2012). Doxorubicin-conjugated chimeric polypeptide nanoparticles that respond to mild hyperthermia. Journal of controlled release : official journal of the Controlled Release Society, 159(3), 362–367. https://doi.org/10.1016/j.jconrel.2012.02.030
1477. Mérian, J., Gravier, J., Navarro, F., & Texier, I. (2012). Fluorescent nanoprobes dedicated to in vivo imaging: from preclinical validations to clinical translation. Molecules (Basel, Switzerland), 17(5), 5564–5591. https://doi.org/10.3390/molecules17055564
1478. de Faria, T. J., Roman, M., de Souza, N. M., De Vecchi, R., de Assis, J. V., dos Santos, A. L., Bechtold, I. H., Winter, N., Soares, M. J., Silva, L. P., De Almeida, M. V., & Báfica, A. (2012). An isoniazid analogue promotes Mycobacterium tuberculosis-nanoparticle interactions and enhances bacterial killing by macrophages. Antimicrobial agents and chemotherapy, 56(5), 2259–2267. https://doi.org/10.1128/AAC.05993-11
1479. González-Toro, D. C., Ryu, J. H., Chacko, R. T., Zhuang, J., & Thayumanavan, S. (2012). Concurrent binding and delivery of proteins and lipophilic small molecules using polymeric nanogels. Journal of the American Chemical Society, 134(16), 6964–6967. https://doi.org/10.1021/ja3019143
1480. Zhu, L., Kate, P., & Torchilin, V. P. (2012). Matrix metalloprotease 2-responsive multifunctional liposomal nanocarrier for enhanced tumor targeting. ACS nano, 6(4), 3491–3498. https://doi.org/10.1021/nn300524f
1481. Sunoqrot, S., Bae, J. W., Pearson, R. M., Shyu, K., Liu, Y., Kim, D. H., & Hong, S. (2012). Temporal control over cellular targeting through hybridization of folate-targeted dendrimers and PEG-PLA nanoparticles. Biomacromolecules, 13(4), 1223–1230. https://doi.org/10.1021/bm300316n
1482. Chauhan, V. P., Stylianopoulos, T., Martin, J. D., Popović, Z., Chen, O., Kamoun, W. S., Bawendi, M. G., Fukumura, D., & Jain, R. K. (2012). Normalization of tumour blood vessels improves the delivery of nanomedicines in a size-dependent manner. Nature nanotechnology, 7(6), 383–388. https://doi.org/10.1038/nnano.2012.45
1483. Mout, R., Moyano, D. F., Rana, S., & Rotello, V. M. (2012). Surface functionalization of nanoparticles for nanomedicine. Chemical Society reviews, 41(7), 2539–2544. https://doi.org/10.1039/c2cs15294k
1484. Kamaly, N., Xiao, Z., Valencia, P. M., Radovic-Moreno, A. F., & Farokhzad, O. C. (2012). Targeted polymeric therapeutic nanoparticles: design, development and clinical translation. Chemical Society reviews, 41(7), 2971–3010. https://doi.org/10.1039/c2cs15344k
1485. Xiao, Y., Hong, H., Javadi, A., Engle, J. W., Xu, W., Yang, Y., Zhang, Y., Barnhart, T. E., Cai, W., & Gong, S. (2012). Multifunctional unimolecular micelles for cancer-targeted drug delivery and positron emission tomography imaging. Biomaterials, 33(11), 3071–3082. https://doi.org/10.1016/j.biomaterials.2011.12.030
1486. Dreaden, E. C., Austin, L. A., Mackey, M. A., & El-Sayed, M. A. (2012). Size matters: gold nanoparticles in targeted cancer drug delivery. Therapeutic delivery, 3(4), 457–478. https://doi.org/10.4155/tde.12.21
1487. Ashley, C. E., Carnes, E. C., Epler, K. E., Padilla, D. P., Phillips, G. K., Castillo, R. E., Wilkinson, D. C., Wilkinson, B. S., Burgard, C. A., Kalinich, R. M., Townson, J. L., Chackerian, B., Willman, C. L., Peabody, D. S., Wharton, W., & Brinker, C. J. (2012). Delivery of small interfering RNA by peptide-targeted mesoporous silica nanoparticle-supported lipid bilayers. ACS nano, 6(3), 2174–2188. https://doi.org/10.1021/nn204102q
1488. Sano, D., Berlin, J. M., Pham, T. T., Marcano, D. C., Valdecanas, D. R., Zhou, G., Milas, L., Myers, J. N., & Tour, J. M. (2012). Noncovalent assembly of targeted carbon nanovectors enables synergistic drug and radiation cancer therapy in vivo. ACS nano, 6(3), 2497–2505. https://doi.org/10.1021/nn204885f
1489. Tong, R., & Cheng, J. (2012). Drug-Initiated, Controlled Ring-Opening Polymerization for the Synthesis of Polymer-Drug Conjugates. Macromolecules, 45(5), 2225–2232. https://doi.org/10.1021/ma202581d
1490. Zheng, X., Zhou, F., Wu, B., Chen, W. R., & Xing, D. (2012). Enhanced tumor treatment using biofunctional indocyanine green-containing nanostructure by intratumoral or intravenous injection. Molecular pharmaceutics, 9(3), 514–522. https://doi.org/10.1021/mp200526m
1491. Zhang, N., & Palmer, A. F. (2012). Liposomes surface conjugated with human hemoglobin target delivery to macrophages. Biotechnology and bioengineering, 109(3), 823–829. https://doi.org/10.1002/bit.24340
1492. Dittrich, C., Burckhardt, C. J., & Danuser, G. (2012). Delivery of membrane impermeable cargo into CHO cells by peptide nanoparticles targeted by a protein corona. Biomaterials, 33(9), 2746–2753. https://doi.org/10.1016/j.biomaterials.2011.12.016
1493. Amoozgar, Z., & Yeo, Y. (2012). Recent advances in stealth coating of nanoparticle drug delivery systems. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 4(2), 219–233. https://doi.org/10.1002/wnan.1157
1494. Rayahin, J. E., Buhrman, J. S., & Gemeinhart, R. A. (2012). Hybrid nanocrystals: University of Kentucky US20060280680A1. Expert opinion on therapeutic patents, 22(3), 341–348. https://doi.org/10.1517/13543776.2012.665877
1495. Della Rocca, J., Liu, D., & Lin, W. (2012). Are high drug loading nanoparticles the next step forward for chemotherapy?. Nanomedicine (London, England), 7(3), 303–305. https://doi.org/10.2217/nnm.11.191
1496. Wankhede, M., Bouras, A., Kaluzova, M., & Hadjipanayis, C. G. (2012). Magnetic nanoparticles: an emerging technology for malignant brain tumor imaging and therapy. Expert review of clinical pharmacology, 5(2), 173–186. https://doi.org/10.1586/ecp.12.1
1497. Kontermann R. E. (2012). Dual targeting strategies with bispecific antibodies. mAbs, 4(2), 182–197. https://doi.org/10.4161/mabs.4.2.19000
1498. van de Ven, A. L., Kim, P., Haley, O., Fakhoury, J. R., Adriani, G., Schmulen, J., Moloney, P., Hussain, F., Ferrari, M., Liu, X., Yun, S. H., & Decuzzi, P. (2012). Rapid tumoritropic accumulation of systemically injected plateloid particles and their biodistribution. Journal of controlled release : official journal of the Controlled Release Society, 158(1), 148–155. https://doi.org/10.1016/j.jconrel.2011.10.021
1499. Fan, Z., Shelton, M., Singh, A. K., Senapati, D., Khan, S. A., & Ray, P. C. (2012). Multifunctional plasmonic shell-magnetic core nanoparticles for targeted diagnostics, isolation, and photothermal destruction of tumor cells. ACS nano, 6(2), 1065–1073. https://doi.org/10.1021/nn2045246
1500. Yurt, A., Daaboul, G. G., Connor, J. H., Goldberg, B. B., & Ünlü, M. S. (2012). Single nanoparticle detectors for biological applications. Nanoscale, 4(3), 715–726. https://doi.org/10.1039/c2nr11562j
1501. York, A. W., Zablocki, K. R., Lewis, D. R., Gu, L., Uhrich, K. E., Prud'homme, R. K., & Moghe, P. V. (2012). Kinetically assembled nanoparticles of bioactive macromolecules exhibit enhanced stability and cell-targeted biological efficacy. Advanced materials (Deerfield Beach, Fla.), 24(6), 733–739. https://doi.org/10.1002/adma.201103348
1502. Rana, S., Bajaj, A., Mout, R., & Rotello, V. M. (2012). Monolayer coated gold nanoparticles for delivery applications. Advanced drug delivery reviews, 64(2), 200–216. https://doi.org/10.1016/j.addr.2011.08.006
1503. Chen, K. J., Tang, L., Garcia, M. A., Wang, H., Lu, H., Lin, W. Y., Hou, S., Yin, Q., Shen, C. K., Cheng, J., & Tseng, H. R. (2012). The therapeutic efficacy of camptothecin-encapsulated supramolecular nanoparticles. Biomaterials, 33(4), 1162–1169. https://doi.org/10.1016/j.biomaterials.2011.10.044
1504. Mitra, R. N., Doshi, M., Zhang, X., Tyus, J. C., Bengtsson, N., Fletcher, S., Page, B. D., Turkson, J., Gesquiere, A. J., Gunning, P. T., Walter, G. A., & Santra, S. (2012). An activatable multimodal/multifunctional nanoprobe for direct imaging of intracellular drug delivery. Biomaterials, 33(5), 1500–1508. https://doi.org/10.1016/j.biomaterials.2011.10.068
1505. Lukianova-Hleb, E. Y., Belyanin, A., Kashinath, S., Wu, X., & Lapotko, D. O. (2012). Plasmonic nanobubble-enhanced endosomal escape processes for selective and guided intracellular delivery of chemotherapy to drug-resistant cancer cells. Biomaterials, 33(6), 1821–1826. https://doi.org/10.1016/j.biomaterials.2011.11.015
1506. Rajasekhar Reddy, R., Raghupathi, K. R., Torres, D. A., & Thayumanavan, S. (2012). Stimuli Sensitive Amphiphilic Dendrimers. New journal of chemistry = Nouveau journal de chimie, 36(2), 340–349. https://doi.org/10.1039/C2NJ20879B
1507. Xia, X., Yang, M., Wang, Y., Zheng, Y., Li, Q., Chen, J., & Xia, Y. (2012). Quantifying the coverage density of poly(ethylene glycol) chains on the surface of gold nanostructures. ACS nano, 6(1), 512–522. https://doi.org/10.1021/nn2038516
1508. Choi, K. Y., Liu, G., Lee, S., & Chen, X. (2012). Theranostic nanoplatforms for simultaneous cancer imaging and therapy: current approaches and future perspectives. Nanoscale, 4(2), 330–342. https://doi.org/10.1039/c1nr11277e
1509. Samarajeewa, S., Shrestha, R., Li, Y., & Wooley, K. L. (2012). Degradability of poly(lactic acid)-containing nanoparticles: enzymatic access through a cross-linked shell barrier. Journal of the American Chemical Society, 134(2), 1235–1242. https://doi.org/10.1021/ja2095602
1510. Ghosh, K., Kanapathipillai, M., Korin, N., McCarthy, J. R., & Ingber, D. E. (2012). Polymeric nanomaterials for islet targeting and immunotherapeutic delivery. Nano letters, 12(1), 203–208. https://doi.org/10.1021/nl203334c
1511. Agasti, S. S., Liong, M., Tassa, C., Chung, H. J., Shaw, S. Y., Lee, H., & Weissleder, R. (2012). Supramolecular host-guest interaction for labeling and detection of cellular biomarkers. Angewandte Chemie (International ed. in English), 51(2), 450–454. https://doi.org/10.1002/anie.201105670
1512. Yesilyurt, V., Ramireddy, R., Azagarsamy, M. A., & Thayumanavan, S. (2012). Accessing lipophilic ligands in dendrimer-based amphiphilic supramolecular assemblies for protein-induced disassembly. Chemistry (Weinheim an der Bergstrasse, Germany), 18(1), 223–229. https://doi.org/10.1002/chem.201102727
1513. Li, Y., Wang, J., Wientjes, M. G., & Au, J. L. (2012). Delivery of nanomedicines to extracellular and intracellular compartments of a solid tumor. Advanced drug delivery reviews, 64(1), 29–39. https://doi.org/10.1016/j.addr.2011.04.006
1514. Sargsyan, S. A., Serkova, N. J., Renner, B., Hasebroock, K. M., Larsen, B., Stoldt, C., McFann, K., Pickering, M. C., & Thurman, J. M. (2012). Detection of glomerular complement C3 fragments by magnetic resonance imaging in murine lupus nephritis. Kidney international, 81(2), 152–159. https://doi.org/10.1038/ki.2011.332
1515. Conde, J., Doria, G., & Baptista, P. (2012). Noble metal nanoparticles applications in cancer. Journal of drug delivery, 2012, 751075. https://doi.org/10.1155/2012/751075
1516. Yu, M. K., Park, J., & Jon, S. (2012). Targeting strategies for multifunctional nanoparticles in cancer imaging and therapy. Theranostics, 2(1), 3–44. https://doi.org/10.7150/thno.3463
1517. Li, M., Kim, H. S., Tian, L., Yu, M. K., Jon, S., & Moon, W. K. (2012). Comparison of Two Ultrasmall Superparamagnetic Iron Oxides on Cytotoxicity and MR Imaging of Tumors. Theranostics, 2(1), 76–85. https://doi.org/10.7150/thno.3462
1518. Monteagudo, E., Gándola, Y., González, L., Bregni, C., & Carlucci, A. M. (2012). Development, characterization, and in vitro evaluation of tamoxifen microemulsions. Journal of drug delivery, 2012, 236713. https://doi.org/10.1155/2012/236713
1519. Capretto, L., Mazzitelli, S., Brognara, E., Lampronti, I., Carugo, D., Hill, M., Zhang, X., Gambari, R., & Nastruzzi, C. (2012). Mithramycin encapsulated in polymeric micelles by microfluidic technology as novel therapeutic protocol for beta-thalassemia. International journal of nanomedicine, 7, 307–324. https://doi.org/10.2147/IJN.S25657
1520. Siddiqui, I. A., Adhami, V. M., Chamcheu, J. C., & Mukhtar, H. (2012). Impact of nanotechnology in cancer: emphasis on nanochemoprevention. International journal of nanomedicine, 7, 591–605. https://doi.org/10.2147/IJN.S26026
1521. Sánchez-Moreno, P., Ortega-Vinuesa, J. L., Martín-Rodríguez, A., Boulaiz, H., Marchal-Corrales, J. A., & Peula-García, J. M. (2012). Characterization of different functionalized lipidic nanocapsules as potential drug carriers. International journal of molecular sciences, 13(2), 2405–2424. https://doi.org/10.3390/ijms13022405
1522. Xu, W., Luo, T., Li, P., Zhou, C., Cui, D., Pang, B., Ren, Q., & Fu, S. (2012). RGD-conjugated gold nanorods induce radiosensitization in melanoma cancer cells by downregulating α(v)β₃ expression. International journal of nanomedicine, 7, 915–924. https://doi.org/10.2147/IJN.S28314
1523. Lukianova-Hleb, E. Y., Ren, X., Constantinou, P. E., Danysh, B. P., Shenefelt, D. L., Carson, D. D., Farach-Carson, M. C., Kulchitsky, V. A., Wu, X., Wagner, D. S., & Lapotko, D. O. (2012). Improved cellular specificity of plasmonic nanobubbles versus nanoparticles in heterogeneous cell systems. PloS one, 7(4), e34537. https://doi.org/10.1371/journal.pone.0034537 (Retraction published PLoS One. 2017 Nov 2;12 (11):e0187820)
1524. Sánchez-Moreno, P., Boulaiz, H., Ortega-Vinuesa, J. L., Peula-García, J. M., & Aránega, A. (2012). Novel drug delivery system based on docetaxel-loaded nanocapsules as a therapeutic strategy against breast cancer cells. International journal of molecular sciences, 13(4), 4906–4919. https://doi.org/10.3390/ijms13044906
1525. Iyer, A. K., He, J., & Amiji, M. M. (2012). Image-guided nanosystems for targeted delivery in cancer therapy. Current medicinal chemistry, 19(19), 3230–3240. https://doi.org/10.2174/092986712800784685
1526. Woo, H. N., Chung, H. K., Ju, E. J., Jung, J., Kang, H. W., Lee, S. W., Seo, M. H., Lee, J. S., Lee, J. S., Park, H. J., Song, S. Y., Jeong, S. Y., & Choi, E. K. (2012). Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy. International journal of nanomedicine, 7, 2197–2208. https://doi.org/10.2147/IJN.S29480
1527. Ren, Y., Zhang, H., Chen, B., Cheng, J., Cai, X., Liu, R., Xia, G., Wu, W., Wang, S., Ding, J., Gao, C., Wang, J., Bao, W., Wang, L., Tian, L., Song, H., & Wang, X. (2012). Multifunctional magnetic Fe3O4 nanoparticles combined with chemotherapy and hyperthermia to overcome multidrug resistance. International journal of nanomedicine, 7, 2261–2269. https://doi.org/10.2147/IJN.S29357
1528. Wang, B. L., Gao, X., Men, K., Qiu, J., Yang, B., Gou, M. L., Huang, M. J., Huang, N., Qian, Z. Y., Zhao, X., & Wei, Y. Q. (2012). Treating acute cystitis with biodegradable micelle-encapsulated quercetin. International journal of nanomedicine, 7, 2239–2247. https://doi.org/10.2147/IJN.S29416
1529. Yoshida, M., Takimoto, R., Murase, K., Sato, Y., Hirakawa, M., Tamura, F., Sato, T., Iyama, S., Osuga, T., Miyanishi, K., Takada, K., Hayashi, T., Kobune, M., & Kato, J. (2012). Targeting anticancer drug delivery to pancreatic cancer cells using a fucose-bound nanoparticle approach. PloS one, 7(7), e39545. https://doi.org/10.1371/journal.pone.0039545
1530. Luo, H., Jiang, B., Li, B., Li, Z., Jiang, B. H., & Chen, Y. C. (2012). Kaempferol nanoparticles achieve strong and selective inhibition of ovarian cancer cell viability. International journal of nanomedicine, 7, 3951–3959. https://doi.org/10.2147/IJN.S33670
1531. Fang, L., Chen, B., Liu, S., Wang, R., Hu, S., Xia, G., Tian, Y., & Cai, X. (2012). Synergistic effect of a combination of nanoparticulate Fe3O4 and gambogic acid on phosphatidylinositol 3-kinase/Akt/Bad pathway of LOVO cells. International journal of nanomedicine, 7, 4109–4118. https://doi.org/10.2147/IJN.S32475
1532. Miele, E., Spinelli, G. P., Miele, E., Di Fabrizio, E., Ferretti, E., Tomao, S., & Gulino, A. (2012). Nanoparticle-based delivery of small interfering RNA: challenges for cancer therapy. International journal of nanomedicine, 7, 3637–3657. https://doi.org/10.2147/IJN.S23696
1533. Park, S. J., & Khang, D. (2012). Conformational changes of fibrinogen in dispersed carbon nanotubes. International journal of nanomedicine, 7, 4325–4333. https://doi.org/10.2147/IJN.S33696
1534. Xiao, Y., Hong, H., Matson, V. Z., Javadi, A., Xu, W., Yang, Y., Zhang, Y., Engle, J. W., Nickles, R. J., Cai, W., Steeber, D. A., & Gong, S. (2012). Gold Nanorods Conjugated with Doxorubicin and cRGD for Combined Anticancer Drug Delivery and PET Imaging. Theranostics, 2(8), 757–768. https://doi.org/10.7150/thno.4756
1535. Cheng, M., He, B., Wan, T., Zhu, W., Han, J., Zha, B., Chen, H., Yang, F., Li, Q., Wang, W., Xu, H., & Ye, T. (2012). 5-Fluorouracil nanoparticles inhibit hepatocellular carcinoma via activation of the p53 pathway in the orthotopic transplant mouse model. PloS one, 7(10), e47115. https://doi.org/10.1371/journal.pone.0047115
1536. Zhang, Y., & Lovell, J. F. (2012). Porphyrins as theranostic agents from prehistoric to modern times. Theranostics, 2(9), 905–915. https://doi.org/10.7150/thno.4908
1537. Josefsen, L. B., & Boyle, R. W. (2012). Unique diagnostic and therapeutic roles of porphyrins and phthalocyanines in photodynamic therapy, imaging and theranostics. Theranostics, 2(9), 916–966. https://doi.org/10.7150/thno.4571
1538. Yang, H., Sun, C., Fan, Z., Tian, X., Yan, L., Du, L., Liu, Y., Chen, C., Liang, X. J., Anderson, G. J., Keelan, J. A., Zhao, Y., & Nie, G. (2012). Effects of gestational age and surface modification on materno-fetal transfer of nanoparticles in murine pregnancy. Scientific reports, 2, 847. https://doi.org/10.1038/srep00847
1539. Patil, R., Portilla-Arias, J., Ding, H., Konda, B., Rekechenetskiy, A., Inoue, S., Black, K. L., Holler, E., & Ljubimova, J. Y. (2012). Cellular delivery of doxorubicin via pH-controlled hydrazone linkage using multifunctional nano vehicle based on poly(β-l-malic acid). International journal of molecular sciences, 13(9), 11681–11693. https://doi.org/10.3390/ijms130911681
1540. Lukianova-Hleb, E. Y., Ren, X., Townley, D., Wu, X., Kupferman, M. E., & Lapotko, D. O. (2012). Plasmonic nanobubbles rapidly detect and destroy drug-resistant tumors. Theranostics, 2(10), 976–987. https://doi.org/10.7150/thno.5116
1541. Qian, W. Y., Sun, D. M., Zhu, R. R., Du, X. L., Liu, H., & Wang, S. L. (2012). pH-sensitive strontium carbonate nanoparticles as new anticancer vehicles for controlled etoposide release. International journal of nanomedicine, 7, 5781–5792. https://doi.org/10.2147/IJN.S34773
1542. Zwicke, G. L., Mansoori, G. A., & Jeffery, C. J. (2012). Utilizing the folate receptor for active targeting of cancer nanotherapeutics. Nano reviews, 3, 10.3402/nano.v3i0.18496. https://doi.org/10.3402/nano.v3i0.18496
1543. Luk, B. T., Fang, R. H., & Zhang, L. (2012). Lipid- and polymer-based nanostructures for cancer theranostics. Theranostics, 2(12), 1117–1126. https://doi.org/10.7150/thno.4381
1544. Xu, C., Mu, L., Roes, I., Miranda-Nieves, D., Nahrendorf, M., Ankrum, J. A., Zhao, W., & Karp, J. M. (2011). Nanoparticle-based monitoring of cell therapy. Nanotechnology, 22(49), 494001. https://doi.org/10.1088/0957-4484/22/49/494001
1545. Myung, J. H., Gajjar, K. A., Saric, J., Eddington, D. T., & Hong, S. (2011). Dendrimer-mediated multivalent binding for the enhanced capture of tumor cells. Angewandte Chemie (International ed. in English), 50(49), 11769–11772. https://doi.org/10.1002/anie.201105508
1546. Kudgus, R. A., Bhattacharya, R., & Mukherjee, P. (2011). Cancer nanotechnology: emerging role of gold nanoconjugates. Anti-cancer agents in medicinal chemistry, 11(10), 965–973. https://doi.org/10.2174/187152011797927652
1547. Blanco, E., Hsiao, A., Ruiz-Esparza, G. U., Landry, M. G., Meric-Bernstam, F., & Ferrari, M. (2011). Molecular-targeted nanotherapies in cancer: enabling treatment specificity. Molecular oncology, 5(6), 492–503. https://doi.org/10.1016/j.molonc.2011.10.005
1548. Chauhan, V. P., Popović, Z., Chen, O., Cui, J., Fukumura, D., Bawendi, M. G., & Jain, R. K. (2011). Fluorescent nanorods and nanospheres for real-time in vivo probing of nanoparticle shape-dependent tumor penetration. Angewandte Chemie (International ed. in English), 50(48), 11417–11420. https://doi.org/10.1002/anie.201104449
1549. Hahn, M. E., & Gianneschi, N. C. (2011). Enzyme-directed assembly and manipulation of organic nanomaterials. Chemical communications (Cambridge, England), 47(43), 11814–11821. https://doi.org/10.1039/c1cc15220c
1550. Mullen, D. G., & Banaszak Holl, M. M. (2011). Heterogeneous ligand-nanoparticle distributions: a major obstacle to scientific understanding and commercial translation. Accounts of chemical research, 44(11), 1135–1145. https://doi.org/10.1021/ar1001389
1551. Santra, S., & Perez, J. M. (2011). Selective N-alkylation of β-alanine facilitates the synthesis of a poly(amino acid)-based theranostic nanoagent. Biomacromolecules, 12(11), 3917–3927. https://doi.org/10.1021/bm2009334
1552. Pusic, K., Xu, H., Stridiron, A., Aguilar, Z., Wang, A., & Hui, G. (2011). Blood stage merozoite surface protein conjugated to nanoparticles induce potent parasite inhibitory antibodies. Vaccine, 29(48), 8898–8908. https://doi.org/10.1016/j.vaccine.2011.09.070
1553. Rodríguez, J. A., Luria-Pérez, R., López-Valdés, H. E., Casero, D., Daniels, T. R., Patel, S., Avila, D., Leuchter, R., So, S., Ortiz-Sánchez, E., Bonavida, B., Martínez-Maza, O., Charles, A. C., Pellegrini, M., Helguera, G., & Penichet, M. L. (2011). Lethal iron deprivation induced by non-neutralizing antibodies targeting transferrin receptor 1 in malignant B cells. Leukemia & lymphoma, 52(11), 2169–2178. https://doi.org/10.3109/10428194.2011.596964
1554. Della Rocca, J., Huxford, R. C., Comstock-Duggan, E., & Lin, W. (2011). Polysilsesquioxane nanoparticles for targeted platin-based cancer chemotherapy by triggered release. Angewandte Chemie (International ed. in English), 50(44), 10330–10334. https://doi.org/10.1002/anie.201104510
1555. Lobatto, M. E., Fuster, V., Fayad, Z. A., & Mulder, W. J. (2011). Perspectives and opportunities for nanomedicine in the management of atherosclerosis. Nature reviews. Drug discovery, 10(11), 835–852. https://doi.org/10.1038/nrd3578
1556. Webber, M. J., Newcomb, C. J., Bitton, R., & Stupp, S. I. (2011). Switching of Self-Assembly in a Peptide Nanostructure with a Specific Enzyme. Soft matter, 7(20), 9665–9672. https://doi.org/10.1039/c1sm05610g
1557. Bardhan, R., Lal, S., Joshi, A., & Halas, N. J. (2011). Theranostic nanoshells: from probe design to imaging and treatment of cancer. Accounts of chemical research, 44(10), 936–946. https://doi.org/10.1021/ar200023x
1558. Della Rocca, J., Liu, D., & Lin, W. (2011). Nanoscale metal-organic frameworks for biomedical imaging and drug delivery. Accounts of chemical research, 44(10), 957–968. https://doi.org/10.1021/ar200028a
1559. Perry, J. L., Herlihy, K. P., Napier, M. E., & Desimone, J. M. (2011). PRINT: a novel platform toward shape and size specific nanoparticle theranostics. Accounts of chemical research, 44(10), 990–998. https://doi.org/10.1021/ar2000315
1560. Lee, V. Y., Havenstrite, K., Tjio, M., McNeil, M., Blau, H. M., Miller, R. D., & Sly, J. (2011). Nanogel star polymer architectures: a nanoparticle platform for modular programmable macromolecular self-assembly, intercellular transport, and dual-mode cargo delivery. Advanced materials (Deerfield Beach, Fla.), 23(39), 4509–4515. https://doi.org/10.1002/adma.201102371
1561. Dvir, T., Bauer, M., Schroeder, A., Tsui, J. H., Anderson, D. G., Langer, R., Liao, R., & Kohane, D. S. (2011). Nanoparticles targeting the infarcted heart. Nano letters, 11(10), 4411–4414. https://doi.org/10.1021/nl2025882
1562. Raghupathi, K. R., Azagarsamy, M. A., & Thayumanavan, S. (2011). Guest-release control in enzyme-sensitive, amphiphilic-dendrimer-based nanoparticles through photochemical crosslinking. Chemistry (Weinheim an der Bergstrasse, Germany), 17(42), 11752–11760. https://doi.org/10.1002/chem.201101066
1563. Wang, T., Kulkarni, N., D'Souza, G. G., Petrenko, V. A., & Torchilin, V. P. (2011). On the mechanism of targeting of phage fusion protein-modified nanocarriers: only the binding peptide sequence matters. Molecular pharmaceutics, 8(5), 1720–1728. https://doi.org/10.1021/mp200080h
1564. Kim, J., & Mooney, D. J. (2011). In Vivo Modulation of Dendritic Cells by Engineered Materials: Towards New Cancer Vaccines. Nano today, 6(5), 466–477. https://doi.org/10.1016/j.nantod.2011.08.005
1565. Kievit, F. M., & Zhang, M. (2011). Cancer nanotheranostics: improving imaging and therapy by targeted delivery across biological barriers. Advanced materials (Deerfield Beach, Fla.), 23(36), H217–H247. https://doi.org/10.1002/adma.201102313
1566. Beqa, L., Fan, Z., Singh, A. K., Senapati, D., & Ray, P. C. (2011). Gold nano-popcorn attached SWCNT hybrid nanomaterial for targeted diagnosis and photothermal therapy of human breast cancer cells. ACS applied materials & interfaces, 3(9), 3316–3324. https://doi.org/10.1021/am2004366
1567. Wang, S., Fan, W., Kim, G., Hah, H. J., Lee, Y. E., Kopelman, R., Ethirajan, M., Gupta, A., Goswami, L. N., Pera, P., Morgan, J., & Pandey, R. K. (2011). Novel methods to incorporate photosensitizers into nanocarriers for cancer treatment by photodynamic therapy. Lasers in surgery and medicine, 43(7), 686–695. https://doi.org/10.1002/lsm.21113
1568. Tsai, C. S., Park, J. W., & Chen, L. T. (2011). Nanovector-based therapies in advanced pancreatic cancer. Journal of gastrointestinal oncology, 2(3), 185–194. https://doi.org/10.3978/j.issn.2078-6891.2011.034
1569. Pabari, R. M., Ryan, B., McCarthy, C., & Ramtoola, Z. (2011). Effect of microencapsulation shear stress on the structural integrity and biological activity of a model monoclonal antibody, trastuzumab. Pharmaceutics, 3(3), 510–524. https://doi.org/10.3390/pharmaceutics3030510
1570. Berlin, J. M., Pham, T. T., Sano, D., Mohamedali, K. A., Marcano, D. C., Myers, J. N., & Tour, J. M. (2011). Noncovalent functionalization of carbon nanovectors with an antibody enables targeted drug delivery. ACS nano, 5(8), 6643–6650. https://doi.org/10.1021/nn2021293
1571. Jalisatgi, S. S., Kulkarni, V. S., Tang, B., Houston, Z. H., Lee, M. W., Jr, & Hawthorne, M. F. (2011). A convenient route to diversely substituted icosahedral closomer nanoscaffolds. Journal of the American Chemical Society, 133(32), 12382–12385. https://doi.org/10.1021/ja204488p
1572. Schädlich, A., Rose, C., Kuntsche, J., Caysa, H., Mueller, T., Göpferich, A., & Mäder, K. (2011). How stealthy are PEG-PLA nanoparticles? An NIR in vivo study combined with detailed size measurements. Pharmaceutical research, 28(8), 1995–2007. https://doi.org/10.1007/s11095-011-0426-5
1573. Li, X., Guo, J., Asong, J., Wolfert, M. A., & Boons, G. J. (2011). Multifunctional surface modification of gold-stabilized nanoparticles by bioorthogonal reactions. Journal of the American Chemical Society, 133(29), 11147–11153. https://doi.org/10.1021/ja2012164
1574. Ashley, C. E., Carnes, E. C., Phillips, G. K., Durfee, P. N., Buley, M. D., Lino, C. A., Padilla, D. P., Phillips, B., Carter, M. B., Willman, C. L., Brinker, C. J., Caldeira, J., Chackerian, B., Wharton, W., & Peabody, D. S. (2011). Cell-specific delivery of diverse cargos by bacteriophage MS2 virus-like particles. ACS nano, 5(7), 5729–5745. https://doi.org/10.1021/nn201397z
1575. Veiseh, O., Kievit, F. M., Ellenbogen, R. G., & Zhang, M. (2011). Cancer cell invasion: treatment and monitoring opportunities in nanomedicine. Advanced drug delivery reviews, 63(8), 582–596. https://doi.org/10.1016/j.addr.2011.01.010
1576. Saha, K., Bajaj, A., Duncan, B., & Rotello, V. M. (2011). Beauty is skin deep: a surface monolayer perspective on nanoparticle interactions with cells and bio-macromolecules. Small (Weinheim an der Bergstrasse, Germany), 7(14), 1903–1918. https://doi.org/10.1002/smll.201100478
1577. Hu, C. M., Zhang, L., Aryal, S., Cheung, C., Fang, R. H., & Zhang, L. (2011). Erythrocyte membrane-camouflaged polymeric nanoparticles as a biomimetic delivery platform. Proceedings of the National Academy of Sciences of the United States of America, 108(27), 10980–10985. https://doi.org/10.1073/pnas.1106634108
1578. Smith, A. H., Robinson, E. M., Zhang, X. Q., Chow, E. K., Lin, Y., Osawa, E., Xi, J., & Ho, D. (2011). Triggered release of therapeutic antibodies from nanodiamond complexes. Nanoscale, 3(7), 2844–2848. https://doi.org/10.1039/c1nr10278h
1579. Kampen K. R. (2011). Membrane proteins: the key players of a cancer cell. The Journal of membrane biology, 242(2), 69–74. https://doi.org/10.1007/s00232-011-9381-7
1580. Dabbagh, A., & Rajaei, S. (2011). Halothane: Is there still any place for using the gas as an anesthetic?. Hepatitis monthly, 11(7), 511–512.
1581. Zhou, K., Wang, Y., Huang, X., Luby-Phelps, K., Sumer, B. D., & Gao, J. (2011). Tunable, ultrasensitive pH-responsive nanoparticles targeting specific endocytic organelles in living cells. Angewandte Chemie (International ed. in English), 50(27), 6109–6114. https://doi.org/10.1002/anie.201100884
1582. Ku, T. H., Chien, M. P., Thompson, M. P., Sinkovits, R. S., Olson, N. H., Baker, T. S., & Gianneschi, N. C. (2011). Controlling and switching the morphology of micellar nanoparticles with enzymes. Journal of the American Chemical Society, 133(22), 8392–8395. https://doi.org/10.1021/ja2004736
1583. Yang, X., Hong, H., Grailer, J. J., Rowland, I. J., Javadi, A., Hurley, S. A., Xiao, Y., Yang, Y., Zhang, Y., Nickles, R. J., Cai, W., Steeber, D. A., & Gong, S. (2011). cRGD-functionalized, DOX-conjugated, and ⁶⁴Cu-labeled superparamagnetic iron oxide nanoparticles for targeted anticancer drug delivery and PET/MR imaging. Biomaterials, 32(17), 4151–4160. https://doi.org/10.1016/j.biomaterials.2011.02.006
1584. Zasadzinski, J. A., Wong, B., Forbes, N., Braun, G., & Wu, G. (2011). Novel Methods of Enhanced Retention in and Rapid, Targeted Release from Liposomes. Current opinion in colloid & interface science, 16(3), 203–214. https://doi.org/10.1016/j.cocis.2010.12.004
1585. Qin, M., Hah, H. J., Kim, G., Nie, G., Lee, Y. E., & Kopelman, R. (2011). Methylene blue covalently loaded polyacrylamide nanoparticles for enhanced tumor-targeted photodynamic therapy. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 10(5), 832–841. https://doi.org/10.1039/c1pp05022b
1586. Ashley, C. E., Carnes, E. C., Phillips, G. K., Padilla, D., Durfee, P. N., Brown, P. A., Hanna, T. N., Liu, J., Phillips, B., Carter, M. B., Carroll, N. J., Jiang, X., Dunphy, D. R., Willman, C. L., Petsev, D. N., Evans, D. G., Parikh, A. N., Chackerian, B., Wharton, W., Peabody, D. S., … Brinker, C. J. (2011). The targeted delivery of multicomponent cargos to cancer cells by nanoporous particle-supported lipid bilayers. Nature materials, 10(5), 389–397. https://doi.org/10.1038/nmat2992
1587. Zdetsis A. D. (2011). Designing novel Sn-Bi, Si-C and Ge-C nanostructures, using simple theoretical chemical similarities. Nanoscale research letters, 6(1), 362. https://doi.org/10.1186/1556-276X-6-362
1588. Mullen, D. G., McNerny, D. Q., Desai, A., Cheng, X. M., Dimaggio, S. C., Kotlyar, A., Zhong, Y., Qin, S., Kelly, C. V., Thomas, T. P., Majoros, I., Orr, B. G., Baker, J. R., & Banaszak Holl, M. M. (2011). Design, synthesis, and biological functionality of a dendrimer-based modular drug delivery platform. Bioconjugate chemistry, 22(4), 679–689. https://doi.org/10.1021/bc100360v
1589. Choi, C. H., Zuckerman, J. E., Webster, P., & Davis, M. E. (2011). Targeting kidney mesangium by nanoparticles of defined size. Proceedings of the National Academy of Sciences of the United States of America, 108(16), 6656–6661. https://doi.org/10.1073/pnas.1103573108
1590. Zhang, Y., Thomas, T. P., Lee, K. H., Li, M., Zong, H., Desai, A. M., Kotlyar, A., Huang, B., Holl, M. M., & Baker, J. R., Jr (2011). Polyvalent saccharide-functionalized generation 3 poly(amidoamine) dendrimer-methotrexate conjugate as a potential anticancer agent. Bioorganic & medicinal chemistry, 19(8), 2557–2564. https://doi.org/10.1016/j.bmc.2011.03.019
1591. Qin, G., Li, Z., Xia, R., Li, F., O'Neill, B. E., Goodwin, J. T., Khant, H. A., Chiu, W., & Li, K. C. (2011). Partially polymerized liposomes: stable against leakage yet capable of instantaneous release for remote controlled drug delivery. Nanotechnology, 22(15), 155605. https://doi.org/10.1088/0957-4484/22/15/155605
1592. Jones, T., & Saba, N. (2011). Nanotechnology and drug delivery: an update in oncology. Pharmaceutics, 3(2), 171–185. https://doi.org/10.3390/pharmaceutics3020171
1593. Bae, K. H., Chung, H. J., & Park, T. G. (2011). Nanomaterials for cancer therapy and imaging. Molecules and cells, 31(4), 295–302. https://doi.org/10.1007/s10059-011-0051-5
1594. Lovell, J. F., Jin, C. S., Huynh, E., Jin, H., Kim, C., Rubinstein, J. L., Chan, W. C., Cao, W., Wang, L. V., & Zheng, G. (2011). Porphysome nanovesicles generated by porphyrin bilayers for use as multimodal biophotonic contrast agents. Nature materials, 10(4), 324–332. https://doi.org/10.1038/nmat2986
1595. Cywińska, M. A., Grudziński, I. P., Cieszanowski, A., Bystrzejewski, M., & Popławska, M. (2011). Nanoplatforms for magnetic resonance imaging of cancer. Polish journal of radiology, 76(2), 28–36.
1596. Rhee, M., Valencia, P. M., Rodriguez, M. I., Langer, R., Farokhzad, O. C., & Karnik, R. (2011). Synthesis of size-tunable polymeric nanoparticles enabled by 3D hydrodynamic flow focusing in single-layer microchannels. Advanced materials (Deerfield Beach, Fla.), 23(12), H79–H83. https://doi.org/10.1002/adma.201004333
1597. Sunoqrot, S., Bae, J. W., Jin, S. E., M Pearson, R., Liu, Y., & Hong, S. (2011). Kinetically controlled cellular interactions of polymer-polymer and polymer-liposome nanohybrid systems. Bioconjugate chemistry, 22(3), 466–474. https://doi.org/10.1021/bc100484t
1598. Jelveh, S., & Chithrani, D. B. (2011). Gold nanostructures as a platform for combinational therapy in future cancer therapeutics. Cancers, 3(1), 1081–1110. https://doi.org/10.3390/cancers3011081
1599. Cheng, Y., Meyers, J. D., Broome, A. M., Kenney, M. E., Basilion, J. P., & Burda, C. (2011). Deep penetration of a PDT drug into tumors by noncovalent drug-gold nanoparticle conjugates. Journal of the American Chemical Society, 133(8), 2583–2591. https://doi.org/10.1021/ja108846h
1600. Hariri, G., Wellons, M. S., Morris, W. H., 3rd, Lukehart, C. M., & Hallahan, D. E. (2011). Multifunctional FePt nanoparticles for radiation-guided targeting and imaging of cancer. Annals of biomedical engineering, 39(3), 946–952. https://doi.org/10.1007/s10439-010-0219-8
1601. Demers, M., Ho-Tin-Noé, B., Schatzberg, D., Yang, J. J., & Wagner, D. D. (2011). Increased efficacy of breast cancer chemotherapy in thrombocytopenic mice. Cancer research, 71(5), 1540–1549. https://doi.org/10.1158/0008-5472.CAN-10-2038
1602. Kato H. (2011). In vitro assays: Tracking nanoparticles inside cells. Nature nanotechnology, 6(3), 139–140. https://doi.org/10.1038/nnano.2011.25
1603. Yigit, M. V., Zhu, L., Ifediba, M. A., Zhang, Y., Carr, K., Moore, A., & Medarova, Z. (2011). Noninvasive MRI-SERS imaging in living mice using an innately bimodal nanomaterial. ACS nano, 5(2), 1056–1066. https://doi.org/10.1021/nn102587h
1604. Sherlock, S. P., Tabakman, S. M., Xie, L., & Dai, H. (2011). Photothermally enhanced drug delivery by ultrasmall multifunctional FeCo/graphitic shell nanocrystals. ACS nano, 5(2), 1505–1512. https://doi.org/10.1021/nn103415x
1605. Diop-Frimpong, B., Chauhan, V. P., Krane, S., Boucher, Y., & Jain, R. K. (2011). Losartan inhibits collagen I synthesis and improves the distribution and efficacy of nanotherapeutics in tumors. Proceedings of the National Academy of Sciences of the United States of America, 108(7), 2909–2914. https://doi.org/10.1073/pnas.1018892108
1606. Kim, J., Cao, L., Shvartsman, D., Silva, E. A., & Mooney, D. J. (2011). Targeted delivery of nanoparticles to ischemic muscle for imaging and therapeutic angiogenesis. Nano letters, 11(2), 694–700. https://doi.org/10.1021/nl103812a
1607. Farrell, D., Ptak, K., Panaro, N. J., & Grodzinski, P. (2011). Nanotechnology-based cancer therapeutics--promise and challenge--lessons learned through the NCI Alliance for Nanotechnology in Cancer. Pharmaceutical research, 28(2), 273–278. https://doi.org/10.1007/s11095-010-0214-7
1608. Bhattacharyya, S., Kudgus, R. A., Bhattacharya, R., & Mukherjee, P. (2011). Inorganic nanoparticles in cancer therapy. Pharmaceutical research, 28(2), 237–259. https://doi.org/10.1007/s11095-010-0318-0
1609. Banerjee, D., Harfouche, R., & Sengupta, S. (2011). Nanotechnology-mediated targeting of tumor angiogenesis. Vascular cell, 3(1), 3. https://doi.org/10.1186/2045-824X-3-3
1610. Johnson, J. A., Lu, Y. Y., Burts, A. O., Lim, Y. H., Finn, M. G., Koberstein, J. T., Turro, N. J., Tirrell, D. A., & Grubbs, R. H. (2011). Core-clickable PEG-branch-azide bivalent-bottle-brush polymers by ROMP: grafting-through and clicking-to. Journal of the American Chemical Society, 133(3), 559–566. https://doi.org/10.1021/ja108441d
1611. Tan, M., & Lu, Z. R. (2011). Integrin Targeted MR Imaging. Theranostics, 1, 83–101. https://doi.org/10.7150/thno/v01p0083
1612. Iancu, C., Mocan, L., Bele, C., Orza, A. I., Tabaran, F. A., Catoi, C., Stiufiuc, R., Stir, A., Matea, C., Iancu, D., Agoston-Coldea, L., Zaharie, F., & Mocan, T. (2011). Enhanced laser thermal ablation for the in vitro treatment of liver cancer by specific delivery of multiwalled carbon nanotubes functionalized with human serum albumin. International journal of nanomedicine, 6, 129–141. https://doi.org/10.2147/IJN.S15841
1613. Floyd, W. C., 3rd, Datta, G. K., Imamura, S., Kieler-Ferguson, H. M., Jerger, K., Patterson, A. W., Fox, M. E., Szoka, F. C., Fréchet, J. M., & Ellman, J. A. (2011). Chemotherapeutic evaluation of a synthetic tubulysin analogue-dendrimer conjugate in c26 tumor bearing mice. ChemMedChem, 6(1), 49–53. https://doi.org/10.1002/cmdc.201000377
1614. Zhang, M., Guo, R., Wang, Y., Cao, X., Shen, M., & Shi, X. (2011). Multifunctional dendrimer/combretastatin A4 inclusion complexes enable in vitro targeted cancer therapy. International journal of nanomedicine, 6, 2337–2349. https://doi.org/10.2147/IJN.S24705
1615. Kateb, B., Chiu, K., Black, K. L., Yamamoto, V., Khalsa, B., Ljubimova, J. Y., Ding, H., Patil, R., Portilla-Arias, J. A., Modo, M., Moore, D. F., Farahani, K., Okun, M. S., Prakash, N., Neman, J., Ahdoot, D., Grundfest, W., Nikzad, S., & Heiss, J. D. (2011). Nanoplatforms for constructing new approaches to cancer treatment, imaging, and drug delivery: what should be the policy?. NeuroImage, 54 Suppl 1(Suppl 1), S106–S124. https://doi.org/10.1016/j.neuroimage.2010.01.105
1616. Yang, L. M., & Blount, P. (2011). Manipulating the permeation of charged compounds through the MscL nanovalve. FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 25(1), 428–434. https://doi.org/10.1096/fj.10-170076
1617. Dinarvand, R., Sepehri, N., Manoochehri, S., Rouhani, H., & Atyabi, F. (2011). Polylactide-co-glycolide nanoparticles for controlled delivery of anticancer agents. International journal of nanomedicine, 6, 877–895. https://doi.org/10.2147/IJN.S18905
1618. Zhang, Y., Hong, H., & Cai, W. (2011). Tumor-targeted drug delivery with aptamers. Current medicinal chemistry, 18(27), 4185–4194. https://doi.org/10.2174/092986711797189547
1619. Boso, D. P., Lee, S. Y., Ferrari, M., Schrefler, B. A., & Decuzzi, P. (2011). Optimizing particle size for targeting diseased microvasculature: from experiments to artificial neural networks. International journal of nanomedicine, 6, 1517–1526. https://doi.org/10.2147/IJN.S20283
1620. Chen, W., & Hu, S. (2011). Suitable carriers for encapsulation and distribution of endostar: comparison of endostar-loaded particulate carriers. International journal of nanomedicine, 6, 1535–1541. https://doi.org/10.2147/IJN.S21881
1621. Liu, Y., Zhang, B., & Yan, B. (2011). Enabling anticancer therapeutics by nanoparticle carriers: the delivery of Paclitaxel. International journal of molecular sciences, 12(7), 4395–4413. https://doi.org/10.3390/ijms12074395
1622. Arvizo, R. R., Miranda, O. R., Moyano, D. F., Walden, C. A., Giri, K., Bhattacharya, R., Robertson, J. D., Rotello, V. M., Reid, J. M., & Mukherjee, P. (2011). Modulating pharmacokinetics, tumor uptake and biodistribution by engineered nanoparticles. PloS one, 6(9), e24374. https://doi.org/10.1371/journal.pone.0024374
1623. Nacev, A., Kim, S. H., Rodriguez-Canales, J., Tangrea, M. A., Shapiro, B., & Emmert-Buck, M. R. (2011). A dynamic magnetic shift method to increase nanoparticle concentration in cancer metastases: a feasibility study using simulations on autopsy specimens. International journal of nanomedicine, 6, 2907–2923. https://doi.org/10.2147/IJN.S23724
1624. McMahon, S. J., Hyland, W. B., Muir, M. F., Coulter, J. A., Jain, S., Butterworth, K. T., Schettino, G., Dickson, G. R., Hounsell, A. R., O'Sullivan, J. M., Prise, K. M., Hirst, D. G., & Currell, F. J. (2011). Biological consequences of nanoscale energy deposition near irradiated heavy atom nanoparticles. Scientific reports, 1, 18. https://doi.org/10.1038/srep00018
1625. McDaniel, J. R., Callahan, D. J., & Chilkoti, A. (2010). Drug delivery to solid tumors by elastin-like polypeptides. Advanced drug delivery reviews, 62(15), 1456–1467. https://doi.org/10.1016/j.addr.2010.05.004
1626. Lu, W., Singh, A. K., Khan, S. A., Senapati, D., Yu, H., & Ray, P. C. (2010). Gold nano-popcorn-based targeted diagnosis, nanotherapy treatment, and in situ monitoring of photothermal therapy response of prostate cancer cells using surface-enhanced Raman spectroscopy. Journal of the American Chemical Society, 132(51), 18103–18114. https://doi.org/10.1021/ja104924b
1627. Johnson, J. A., Lu, Y. Y., Burts, A. O., Xia, Y., Durrell, A. C., Tirrell, D. A., & Grubbs, R. H. (2010). Drug-loaded, bivalent-bottle-brush polymers by graft-through ROMP. Macromolecules, 43(24), 10326–10335. https://doi.org/10.1021/ma1021506
1628. Lee, S. M., Song, Y., Hong, B. J., MacRenaris, K. W., Mastarone, D. J., O'Halloran, T. V., Meade, T. J., & Nguyen, S. T. (2010). Modular polymer-caged nanobins as a theranostic platform with enhanced magnetic resonance relaxivity and pH-responsive drug release. Angewandte Chemie (International ed. in English), 49(51), 9960–9964. https://doi.org/10.1002/anie.201004867
1629. Nair, H. B., Sung, B., Yadav, V. R., Kannappan, R., Chaturvedi, M. M., & Aggarwal, B. B. (2010). Delivery of antiinflammatory nutraceuticals by nanoparticles for the prevention and treatment of cancer. Biochemical pharmacology, 80(12), 1833–1843. https://doi.org/10.1016/j.bcp.2010.07.021
1630. Lee, S. M., O'Halloran, T. V., & Nguyen, S. T. (2010). Polymer-caged nanobins for synergistic cisplatin-doxorubicin combination chemotherapy. Journal of the American Chemical Society, 132(48), 17130–17138. https://doi.org/10.1021/ja107333g
1631. Bardhan, R., Chen, W., Bartels, M., Perez-Torres, C., Botero, M. F., McAninch, R. W., Contreras, A., Schiff, R., Pautler, R. G., Halas, N. J., & Joshi, A. (2010). Tracking of multimodal therapeutic nanocomplexes targeting breast cancer in vivo. Nano letters, 10(12), 4920–4928. https://doi.org/10.1021/nl102889y
1632. Guo, J., Chen, G., Ning, X., Wolfert, M. A., Li, X., Xu, B., & Boons, G. J. (2010). Surface modification of polymeric micelles by strain-promoted alkyne-azide cycloadditions. Chemistry (Weinheim an der Bergstrasse, Germany), 16(45), 13360–13366. https://doi.org/10.1002/chem.201002532
1633. Jacobson K. A. (2010). GPCR ligand-dendrimer (GLiDe) conjugates: future smart drugs?. Trends in pharmacological sciences, 31(12), 575–579. https://doi.org/10.1016/j.tips.2010.09.002
1634. Choi, H. S., & Frangioni, J. V. (2010). Nanoparticles for biomedical imaging: fundamentals of clinical translation. Molecular imaging, 9(6), 291–310.
1635. Kumar, R., Ohulchanskyy, T. Y., Turowski, S. G., Thompson, M. E., Seshadri, M., & Prasad, P. N. (2010). Combined magnetic resonance and optical imaging of head and neck tumor xenografts using Gadolinium-labelled phosphorescent polymeric nanomicelles. Head & neck oncology, 2, 35. https://doi.org/10.1186/1758-3284-2-35
1636. Hu, S., & Zhang, Y. (2010). Endostar-loaded PEG-PLGA nanoparticles: in vitro and in vivo evaluation. International journal of nanomedicine, 5, 1039–1048. https://doi.org/10.2147/IJN.S14753
1637. Cobley, C. M., & Xia, Y. (2010). Engineering the Properties of Metal Nanostructures via Galvanic Replacement Reactions. Materials science & engineering. R, Reports : a review journal, 70(3-6), 44–62. https://doi.org/10.1016/j.mser.2010.06.002
1638. Duncan, B., Kim, C., & Rotello, V. M. (2010). Gold nanoparticle platforms as drug and biomacromolecule delivery systems. Journal of controlled release : official journal of the Controlled Release Society, 148(1), 122–127. https://doi.org/10.1016/j.jconrel.2010.06.004
1639. Chen, J., Yang, M., Zhang, Q., Cho, E. C., Cobley, C. M., Kim, C., Glaus, C., Wang, L. V., Welch, M. J., & Xia, Y. (2010). Gold Nanocages: A Novel Class of Multifunctional Nanomaterials for Theranostic Applications. Advanced functional materials, 20(21), 3684–3694. https://doi.org/10.1002/adfm.201001329
1640. Patil, R., Portilla-Arias, J., Ding, H., Inoue, S., Konda, B., Hu, J., Wawrowsky, K. A., Shin, P. K., Black, K. L., Holler, E., & Ljubimova, J. Y. (2010). Temozolomide delivery to tumor cells by a multifunctional nano vehicle based on poly(β-L-malic acid). Pharmaceutical research, 27(11), 2317–2329. https://doi.org/10.1007/s11095-010-0091-0
1641. Johnson-Lyles, D. N., Peifley, K., Lockett, S., Neun, B. W., Hansen, M., Clogston, J., Stern, S. T., & McNeil, S. E. (2010). Fullerenol cytotoxicity in kidney cells is associated with cytoskeleton disruption, autophagic vacuole accumulation, and mitochondrial dysfunction. Toxicology and applied pharmacology, 248(3), 249–258. https://doi.org/10.1016/j.taap.2010.08.008
1642. Fang, C., Veiseh, O., Kievit, F., Bhattarai, N., Wang, F., Stephen, Z., Li, C., Lee, D., Ellenbogen, R. G., & Zhang, M. (2010). Functionalization of iron oxide magnetic nanoparticles with targeting ligands: their physicochemical properties and in vivo behavior. Nanomedicine (London, England), 5(9), 1357–1369. https://doi.org/10.2217/nnm.10.55
1643. Vuorela, T., Catte, A., Niemelä, P. S., Hall, A., Hyvönen, M. T., Marrink, S. J., Karttunen, M., & Vattulainen, I. (2010). Role of lipids in spheroidal high density lipoproteins. PLoS computational biology, 6(10), e1000964. https://doi.org/10.1371/journal.pcbi.1000964
1644. Rudra, A., Deepa, R. M., Ghosh, M. K., Ghosh, S., & Mukherjee, B. (2010). Doxorubicin-loaded phosphatidylethanolamine-conjugated nanoliposomes: in vitro characterization and their accumulation in liver, kidneys, and lungs in rats. International journal of nanomedicine, 5, 811–823. https://doi.org/10.2147/IJN.S13031
1645. Hariri, G., Yan, H., Wang, H., Han, Z., & Hallahan, D. E. (2010). Radiation-guided drug delivery to mouse models of lung cancer. Clinical cancer research : an official journal of the American Association for Cancer Research, 16(20), 4968–4977. https://doi.org/10.1158/1078-0432.CCR-10-0969
1646. Yu, B., Tai, H. C., Xue, W., Lee, L. J., & Lee, R. J. (2010). Receptor-targeted nanocarriers for therapeutic delivery to cancer. Molecular membrane biology, 27(7), 286–298. https://doi.org/10.3109/09687688.2010.521200
1647. Capurso, N. A., Look, M., Jeanbart, L., Nowyhed, H., Abraham, C., Craft, J., & Fahmy, T. M. (2010). Development of a nanoparticulate formulation of retinoic acid that suppresses Th17 cells and upregulates regulatory T cells. Self/nonself, 1(4), 335–340. https://doi.org/10.4161/self.1.4.13946
1648. Lee, S. M., Ahn, R. W., Chen, F., Fought, A. J., O'Halloran, T. V., Cryns, V. L., & Nguyen, S. T. (2010). Biological evaluation of pH-responsive polymer-caged nanobins for breast cancer therapy. ACS nano, 4(9), 4971–4978. https://doi.org/10.1021/nn100560p
1649. Gao, W., Liu, W., Christensen, T., Zalutsky, M. R., & Chilkoti, A. (2010). In situ growth of a PEG-like polymer from the C terminus of an intein fusion protein improves pharmacokinetics and tumor accumulation. Proceedings of the National Academy of Sciences of the United States of America, 107(38), 16432–16437. https://doi.org/10.1073/pnas.1006044107
1650. Braun, K., Wiessler, M., Pipkorn, R., Ehemann, V., Bäuerle, T., Fleischhacker, H., Müller, G., Lorenz, P., & Waldeck, W. (2010). A cyclic-RGD-BioShuttle functionalized with TMZ by DARinv "Click Chemistry" targeted to αvβ3 integrin for therapy. International journal of medical sciences, 7(6), 326–339. https://doi.org/10.7150/ijms.7.326
1651. Mullen, D. G., Borgmeier, E. L., Desai, A. M., van Dongen, M. A., Barash, M., Cheng, X. M., Baker, J. R., Jr, & Banaszak Holl, M. M. (2010). Isolation and characterization of dendrimers with precise numbers of functional groups. Chemistry (Weinheim an der Bergstrasse, Germany), 16(35), 10675–10678. https://doi.org/10.1002/chem.201001175
1652. Jin, S. E., Bae, J. W., & Hong, S. (2010). Multiscale observation of biological interactions of nanocarriers: from nano to macro. Microscopy research and technique, 73(9), 813–823. https://doi.org/10.1002/jemt.20847
1653. Kim, T. H., Chen, Y., Mount, C. W., Gombotz, W. R., Li, X., & Pun, S. H. (2010). Evaluation of temperature-sensitive, indocyanine green-encapsulating micelles for noninvasive near-infrared tumor imaging. Pharmaceutical research, 27(9), 1900–1913. https://doi.org/10.1007/s11095-010-0190-y
1654. Haun, J. B., Devaraj, N. K., Hilderbrand, S. A., Lee, H., & Weissleder, R. (2010). Bioorthogonal chemistry amplifies nanoparticle binding and enhances the sensitivity of cell detection. Nature nanotechnology, 5(9), 660–665. https://doi.org/10.1038/nnano.2010.148
1655. Mullen, D. G., Borgmeier, E. L., Fang, M., McNerny, D. Q., Desai, A., Baker, J. R., Jr, Orr, B. G., & Holl, M. M. (2010). Effect of Mass Transport in the Synthesis of Partially Acetylated Dendrimer: Implications for Functional Ligand-Nanoparticle Distributions. Macromolecules, 43(16), 6577–6587. https://doi.org/10.1021/ma100663c
1656. Roos, W. H., Gibbons, M. M., Arkhipov, A., Uetrecht, C., Watts, N. R., Wingfield, P. T., Steven, A. C., Heck, A. J., Schulten, K., Klug, W. S., & Wuite, G. J. (2010). Squeezing protein shells: how continuum elastic models, molecular dynamics simulations, and experiments coalesce at the nanoscale. Biophysical journal, 99(4), 1175–1181. https://doi.org/10.1016/j.bpj.2010.05.033
1657. Sahay, G., Alakhova, D. Y., & Kabanov, A. V. (2010). Endocytosis of nanomedicines. Journal of controlled release : official journal of the Controlled Release Society, 145(3), 182–195. https://doi.org/10.1016/j.jconrel.2010.01.036
1658. Sakamoto, J. H., van de Ven, A. L., Godin, B., Blanco, E., Serda, R. E., Grattoni, A., Ziemys, A., Bouamrani, A., Hu, T., Ranganathan, S. I., De Rosa, E., Martinez, J. O., Smid, C. A., Buchanan, R. M., Lee, S. Y., Srinivasan, S., Landry, M., Meyn, A., Tasciotti, E., Liu, X., … Ferrari, M. (2010). Enabling individualized therapy through nanotechnology. Pharmacological research, 62(2), 57–89. https://doi.org/10.1016/j.phrs.2009.12.011
1659. Zhang, J., & Ma, P. X. (2010). Host-guest interactions mediated nano-assemblies using cyclodextrin-containing hydrophilic polymers and their biomedical applications. Nano today, 5(4), 337–350. https://doi.org/10.1016/j.nantod.2010.06.011
1660. Luo, J., Xiao, K., Li, Y., Lee, J. S., Shi, L., Tan, Y. H., Xing, L., Holland Cheng, R., Liu, G. Y., & Lam, K. S. (2010). Well-defined, size-tunable, multifunctional micelles for efficient paclitaxel delivery for cancer treatment. Bioconjugate chemistry, 21(7), 1216–1224. https://doi.org/10.1021/bc1000033
1661. Ahn, R. W., Chen, F., Chen, H., Stern, S. T., Clogston, J. D., Patri, A. K., Raja, M. R., Swindell, E. P., Parimi, V., Cryns, V. L., & O'Halloran, T. V. (2010). A novel nanoparticulate formulation of arsenic trioxide with enhanced therapeutic efficacy in a murine model of breast cancer. Clinical cancer research : an official journal of the American Association for Cancer Research, 16(14), 3607–3617. https://doi.org/10.1158/1078-0432.CCR-10-0068
1662. Thompson, M. P., Chien, M. P., Ku, T. H., Rush, A. M., & Gianneschi, N. C. (2010). Smart lipids for programmable nanomaterials. Nano letters, 10(7), 2690–2693. https://doi.org/10.1021/nl101640k
1663. Chien, M. P., Rush, A. M., Thompson, M. P., & Gianneschi, N. C. (2010). Programmable shape-shifting micelles. Angewandte Chemie (International ed. in English), 49(30), 5076–5080. https://doi.org/10.1002/anie.201000265
1664. MacEwan, S. R., Callahan, D. J., & Chilkoti, A. (2010). Stimulus-responsive macromolecules and nanoparticles for cancer drug delivery. Nanomedicine (London, England), 5(5), 793–806. https://doi.org/10.2217/nnm.10.50
1665. Febvay, S., Marini, D. M., Belcher, A. M., & Clapham, D. E. (2010). Targeted cytosolic delivery of cell-impermeable compounds by nanoparticle-mediated, light-triggered endosome disruption. Nano letters, 10(6), 2211–2219. https://doi.org/10.1021/nl101157z
1666. Siddiqui, I. A., & Mukhtar, H. (2010). Nanochemoprevention by bioactive food components: a perspective. Pharmaceutical research, 27(6), 1054–1060. https://doi.org/10.1007/s11095-010-0087-9
1667. Arvizo, R., Bhattacharya, R., & Mukherjee, P. (2010). Gold nanoparticles: opportunities and challenges in nanomedicine. Expert opinion on drug delivery, 7(6), 753–763. https://doi.org/10.1517/17425241003777010
1668. Wang, T., D'Souza, G. G., Bedi, D., Fagbohun, O. A., Potturi, L. P., Papahadjopoulos-Sternberg, B., Petrenko, V. A., & Torchilin, V. P. (2010). Enhanced binding and killing of target tumor cells by drug-loaded liposomes modified with tumor-specific phage fusion coat protein. Nanomedicine (London, England), 5(4), 563–574. https://doi.org/10.2217/nnm.10.30
1669. Dong, X., & Mumper, R. J. (2010). Nanomedicinal strategies to treat multidrug-resistant tumors: current progress. Nanomedicine (London, England), 5(4), 597–615. https://doi.org/10.2217/nnm.10.35
1670. Blanco, E., Bey, E. A., Khemtong, C., Yang, S. G., Setti-Guthi, J., Chen, H., Kessinger, C. W., Carnevale, K. A., Bornmann, W. G., Boothman, D. A., & Gao, J. (2010). Beta-lapachone micellar nanotherapeutics for non-small cell lung cancer therapy. Cancer research, 70(10), 3896–3904. https://doi.org/10.1158/0008-5472.CAN-09-3995
1671. Chanda, N., Kattumuri, V., Shukla, R., Zambre, A., Katti, K., Upendran, A., Kulkarni, R. R., Kan, P., Fent, G. M., Casteel, S. W., Smith, C. J., Boote, E., Robertson, J. D., Cutler, C., Lever, J. R., Katti, K. V., & Kannan, R. (2010). Bombesin functionalized gold nanoparticles show in vitro and in vivo cancer receptor specificity. Proceedings of the National Academy of Sciences of the United States of America, 107(19), 8760–8765. https://doi.org/10.1073/pnas.1002143107
1672. Godin, B., Sakamoto, J. H., Serda, R. E., Grattoni, A., Bouamrani, A., & Ferrari, M. (2010). Emerging applications of nanomedicine for the diagnosis and treatment of cardiovascular diseases. Trends in pharmacological sciences, 31(5), 199–205. https://doi.org/10.1016/j.tips.2010.01.003
1673. Cobley, C. M., Au, L., Chen, J., & Xia, Y. (2010). Targeting gold nanocages to cancer cells for photothermal destruction and drug delivery. Expert opinion on drug delivery, 7(5), 577–587. https://doi.org/10.1517/17425240903571614
1674. Scheinberg, D. A., Villa, C. H., Escorcia, F. E., & McDevitt, M. R. (2010). Conscripts of the infinite armada: systemic cancer therapy using nanomaterials. Nature reviews. Clinical oncology, 7(5), 266–276. https://doi.org/10.1038/nrclinonc.2010.38
1675. Simnick, A. J., Valencia, C. A., Liu, R., & Chilkoti, A. (2010). Morphing low-affinity ligands into high-avidity nanoparticles by thermally triggered self-assembly of a genetically encoded polymer. ACS nano, 4(4), 2217–2227. https://doi.org/10.1021/nn901732h
1676. Tam, J. M., Tam, J. O., Murthy, A., Ingram, D. R., Ma, L. L., Travis, K., Johnston, K. P., & Sokolov, K. V. (2010). Controlled assembly of biodegradable plasmonic nanoclusters for near-infrared imaging and therapeutic applications. ACS nano, 4(4), 2178–2184. https://doi.org/10.1021/nn9015746
1677. van der Poll, D. G., Kieler-Ferguson, H. M., Floyd, W. C., Guillaudeu, S. J., Jerger, K., Szoka, F. C., & Fréchet, J. M. (2010). Design, synthesis, and biological evaluation of a robust, biodegradable dendrimer. Bioconjugate chemistry, 21(4), 764–773. https://doi.org/10.1021/bc900553n
1678. Santra, S., Kaittanis, C., & Perez, J. M. (2010). Aliphatic hyperbranched polyester: a new building block in the construction of multifunctional nanoparticles and nanocomposites. Langmuir : the ACS journal of surfaces and colloids, 26(8), 5364–5373. https://doi.org/10.1021/la9037843
1679. Huxford, R. C., Della Rocca, J., & Lin, W. (2010). Metal-organic frameworks as potential drug carriers. Current opinion in chemical biology, 14(2), 262–268. https://doi.org/10.1016/j.cbpa.2009.12.012
1680. Ferrari M. (2010). Frontiers in cancer nanomedicine: directing mass transport through biological barriers. Trends in biotechnology, 28(4), 181–188. https://doi.org/10.1016/j.tibtech.2009.12.007
1681. Caldorera-Moore, M., Guimard, N., Shi, L., & Roy, K. (2010). Designer nanoparticles: incorporating size, shape and triggered release into nanoscale drug carriers. Expert opinion on drug delivery, 7(4), 479–495. https://doi.org/10.1517/17425240903579971
1682. Valencia, P. M., Basto, P. A., Zhang, L., Rhee, M., Langer, R., Farokhzad, O. C., & Karnik, R. (2010). Single-step assembly of homogenous lipid-polymeric and lipid-quantum dot nanoparticles enabled by microfluidic rapid mixing. ACS nano, 4(3), 1671–1679. https://doi.org/10.1021/nn901433u
1683. Ruoslahti, E., Bhatia, S. N., & Sailor, M. J. (2010). Targeting of drugs and nanoparticles to tumors. The Journal of cell biology, 188(6), 759–768. https://doi.org/10.1083/jcb.200910104
1684. Zhang, Y., Thomas, T. P., Desai, A., Zong, H., Leroueil, P. R., Majoros, I. J., & Baker, J. R., Jr (2010). Targeted dendrimeric anticancer prodrug: a methotrexate-folic acid-poly(amidoamine) conjugate and a novel, rapid, "one pot" synthetic approach. Bioconjugate chemistry, 21(3), 489–495. https://doi.org/10.1021/bc9003958
1685. Lee, M. J., Veiseh, O., Bhattarai, N., Sun, C., Hansen, S. J., Ditzler, S., Knoblaugh, S., Lee, D., Ellenbogen, R., Zhang, M., & Olson, J. M. (2010). Rapid pharmacokinetic and biodistribution studies using cholorotoxin-conjugated iron oxide nanoparticles: a novel non-radioactive method. PloS one, 5(3), e9536. https://doi.org/10.1371/journal.pone.0009536
1686. Zhang, K., Fang, H., Wang, Z., Li, Z., Taylor, J. S., & Wooley, K. L. (2010). Structure-activity relationships of cationic shell-crosslinked knedel-like nanoparticles: shell composition and transfection efficiency/cytotoxicity. Biomaterials, 31(7), 1805–1813. https://doi.org/10.1016/j.biomaterials.2009.10.033
1687. Jarzyna, P. A., Gianella, A., Skajaa, T., Knudsen, G., Deddens, L. H., Cormode, D. P., Fayad, Z. A., & Mulder, W. J. (2010). Multifunctional imaging nanoprobes. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 2(2), 138–150. https://doi.org/10.1002/wnan.72
1688. Mullen, D. G., Fang, M., Desai, A., Baker, J. R., Orr, B. G., & Banaszak Holl, M. M. (2010). A quantitative assessment of nanoparticle-ligand distributions: implications for targeted drug and imaging delivery in dendrimer conjugates. ACS nano, 4(2), 657–670. https://doi.org/10.1021/nn900999c
1689. You, J., Zhang, G., & Li, C. (2010). Exceptionally high payload of doxorubicin in hollow gold nanospheres for near-infrared light-triggered drug release. ACS nano, 4(2), 1033–1041. https://doi.org/10.1021/nn901181c
1690. Cheng, H., Kastrup, C. J., Ramanathan, R., Siegwart, D. J., Ma, M., Bogatyrev, S. R., Xu, Q., Whitehead, K. A., Langer, R., & Anderson, D. G. (2010). Nanoparticulate cellular patches for cell-mediated tumoritropic delivery. ACS nano, 4(2), 625–631. https://doi.org/10.1021/nn901319y
1691. Chan, J. M., Zhang, L., Tong, R., Ghosh, D., Gao, W., Liao, G., Yuet, K. P., Gray, D., Rhee, J. W., Cheng, J., Golomb, G., Libby, P., Langer, R., & Farokhzad, O. C. (2010). Spatiotemporal controlled delivery of nanoparticles to injured vasculature. Proceedings of the National Academy of Sciences of the United States of America, 107(5), 2213–2218. https://doi.org/10.1073/pnas.0914585107
1692. Guthi, J. S., Yang, S. G., Huang, G., Li, S., Khemtong, C., Kessinger, C. W., Peyton, M., Minna, J. D., Brown, K. C., & Gao, J. (2010). MRI-visible micellar nanomedicine for targeted drug delivery to lung cancer cells. Molecular pharmaceutics, 7(1), 32–40. https://doi.org/10.1021/mp9001393
1693. Sahay, G., Kim, J. O., Kabanov, A. V., & Bronich, T. K. (2010). The exploitation of differential endocytic pathways in normal and tumor cells in the selective targeting of nanoparticulate chemotherapeutic agents. Biomaterials, 31(5), 923–933. https://doi.org/10.1016/j.biomaterials.2009.09.101
1694. Horcajada, P., Chalati, T., Serre, C., Gillet, B., Sebrie, C., Baati, T., Eubank, J. F., Heurtaux, D., Clayette, P., Kreuz, C., Chang, J. S., Hwang, Y. K., Marsaud, V., Bories, P. N., Cynober, L., Gil, S., Férey, G., Couvreur, P., & Gref, R. (2010). Porous metal-organic-framework nanoscale carriers as a potential platform for drug delivery and imaging. Nature materials, 9(2), 172–178. https://doi.org/10.1038/nmat2608
1695. Aryal, S., Hu, C. M., & Zhang, L. (2010). Polymer--cisplatin conjugate nanoparticles for acid-responsive drug delivery. ACS nano, 4(1), 251–258. https://doi.org/10.1021/nn9014032
1696. Massodi, I., Moktan, S., Rawat, A., Bidwell, G. L., 3rd, & Raucher, D. (2010). Inhibition of ovarian cancer cell proliferation by a cell cycle inhibitory peptide fused to a thermally responsive polypeptide carrier. International journal of cancer, 126(2), 533–544. https://doi.org/10.1002/ijc.24725
1697. Patil, Y. B., Swaminathan, S. K., Sadhukha, T., Ma, L., & Panyam, J. (2010). The use of nanoparticle-mediated targeted gene silencing and drug delivery to overcome tumor drug resistance. Biomaterials, 31(2), 358–365. https://doi.org/10.1016/j.biomaterials.2009.09.048
1698. Choi, H. S., Liu, W., Liu, F., Nasr, K., Misra, P., Bawendi, M. G., & Frangioni, J. V. (2010). Design considerations for tumour-targeted nanoparticles. Nature nanotechnology, 5(1), 42–47. https://doi.org/10.1038/nnano.2009.314
1699. Dvir, T., Banghart, M. R., Timko, B. P., Langer, R., & Kohane, D. S. (2010). Photo-targeted nanoparticles. Nano letters, 10(1), 250–254. https://doi.org/10.1021/nl903411s
1700. Rajendran, L., Knölker, H. J., & Simons, K. (2010). Subcellular targeting strategies for drug design and delivery. Nature reviews. Drug discovery, 9(1), 29–42. https://doi.org/10.1038/nrd2897
1701. Godin, B., Driessen, W. H., Proneth, B., Lee, S. Y., Srinivasan, S., Rumbaut, R., Arap, W., Pasqualini, R., Ferrari, M., & Decuzzi, P. (2010). An integrated approach for the rational design of nanovectors for biomedical imaging and therapy. Advances in genetics, 69, 31–64. https://doi.org/10.1016/S0065-2660(10)69009-8
1702. Siddiqui, I. A., Adhami, V. M., Ahmad, N., & Mukhtar, H. (2010). Nanochemoprevention: sustained release of bioactive food components for cancer prevention. Nutrition and cancer, 62(7), 883–890. https://doi.org/10.1080/01635581.2010.509537
1703. Portilla-Arias, J., Patil, R., Hu, J., Ding, H., Black, K. L., García-Alvarez, M., Muñoz-Guerra, S., Ljubimova, J. Y., & Holler, E. (2010). Nanoconjugate Platforms Development Based in Poly(β,L-Malic Acid) Methyl Esters for Tumor Drug Delivery. Journal of nanotechnology, 2010, 825363. https://doi.org/10.1155/2010/825363
1704. Kim, Y., Hechler, B., Gao, Z. G., Gachet, C., & Jacobson, K. A. (2009). PEGylated dendritic unimolecular micelles as versatile carriers for ligands of G protein-coupled receptors. Bioconjugate chemistry, 20(10), 1888–1898. https://doi.org/10.1021/bc9001689
1705. Xiao, Y., Gao, X., Taratula, O., Treado, S., Urbas, A., Holbrook, R. D., Cavicchi, R. E., Avedisian, C. T., Mitra, S., Savla, R., Wagner, P. D., Srivastava, S., & He, H. (2009). Anti-HER2 IgY antibody-functionalized single-walled carbon nanotubes for detection and selective destruction of breast cancer cells. BMC cancer, 9, 351. https://doi.org/10.1186/1471-2407-9-351
1706. Liu, J., Jiang, Z., Zhang, S., & Saltzman, W. M. (2009). Poly(omega-pentadecalactone-co-butylene-co-succinate) nanoparticles as biodegradable carriers for camptothecin delivery. Biomaterials, 30(29), 5707–5719. https://doi.org/10.1016/j.biomaterials.2009.06.061
1707. Bhirde, A. A., Sousa, A. A., Patel, V., Azari, A. A., Gutkind, J. S., Leapman, R. D., & Rusling, J. F. (2009). Imaging the distribution of individual platinum-based anticancer drug molecules attached to single-wall carbon nanotubes. Nanomedicine (London, England), 4(7), 763–772. https://doi.org/10.2217/nnm.09.56
1708. Hong, H., Zhang, Y., Sun, J., & Cai, W. (2009). Molecular imaging and therapy of cancer with radiolabeled nanoparticles. Nano today, 4(5), 399–413. https://doi.org/10.1016/j.nantod.2009.07.001
1709. Hanley, C., Thurber, A., Hanna, C., Punnoose, A., Zhang, J., & Wingett, D. G. (2009). The Influences of Cell Type and ZnO Nanoparticle Size on Immune Cell Cytotoxicity and Cytokine Induction. Nanoscale research letters, 4(12), 1409–1420. https://doi.org/10.1007/s11671-009-9413-8
1710. Kim, D., Gao, Z. G., Lee, E. S., & Bae, Y. H. (2009). In vivo evaluation of doxorubicin-loaded polymeric micelles targeting folate receptors and early endosomal pH in drug-resistant ovarian cancer. Molecular pharmaceutics, 6(5), 1353–1362. https://doi.org/10.1021/mp900021q
1711. Rozhkova, E. A., Ulasov, I., Lai, B., Dimitrijevic, N. M., Lesniak, M. S., & Rajh, T. (2009). A high-performance nanobio photocatalyst for targeted brain cancer therapy. Nano letters, 9(9), 3337–3342. https://doi.org/10.1021/nl901610f
1712. Fox, M. E., Szoka, F. C., & Fréchet, J. M. (2009). Soluble polymer carriers for the treatment of cancer: the importance of molecular architecture. Accounts of chemical research, 42(8), 1141–1151. https://doi.org/10.1021/ar900035f
1713. Beaudette, T. T., Cohen, J. A., Bachelder, E. M., Broaders, K. E., Cohen, J. L., Engleman, E. G., & Fréchet, J. M. (2009). Chemoselective ligation in the functionalization of polysaccharide-based particles. Journal of the American Chemical Society, 131(30), 10360–10361. https://doi.org/10.1021/ja903984s
1714. Nasti, A., Zaki, N. M., de Leonardis, P., Ungphaiboon, S., Sansongsak, P., Rimoli, M. G., & Tirelli, N. (2009). Chitosan/TPP and chitosan/TPP-hyaluronic acid nanoparticles: systematic optimisation of the preparative process and preliminary biological evaluation. Pharmaceutical research, 26(8), 1918–1930. https://doi.org/10.1007/s11095-009-9908-0
1715. Mulder, W. J., Strijkers, G. J., van Tilborg, G. A., Cormode, D. P., Fayad, Z. A., & Nicolay, K. (2009). Nanoparticulate assemblies of amphiphiles and diagnostically active materials for multimodality imaging. Accounts of chemical research, 42(7), 904–914. https://doi.org/10.1021/ar800223c
1716. Shi, X., Wang, S. H., Van Antwerp, M. E., Chen, X., & Baker, J. R., Jr (2009). Targeting and detecting cancer cells using spontaneously formed multifunctional dendrimer-stabilized gold nanoparticles. The Analyst, 134(7), 1373–1379. https://doi.org/10.1039/b902199j
1717. Fang, C., Bhattarai, N., Sun, C., & Zhang, M. (2009). Functionalized nanoparticles with long-term stability in biological media. Small (Weinheim an der Bergstrasse, Germany), 5(14), 1637–1641. https://doi.org/10.1002/smll.200801647
1718. Gullotti, E., & Yeo, Y. (2009). Extracellularly activated nanocarriers: a new paradigm of tumor targeted drug delivery. Molecular pharmaceutics, 6(4), 1041–1051. https://doi.org/10.1021/mp900090z
1719. Karagiannis, E. D., & Anderson, D. G. (2009). Minicells overcome tumor drug-resistance. Nature biotechnology, 27(7), 620–621. https://doi.org/10.1038/nbt0709-620
1720. Banerjee, J., Hanson, A. J., Gadam, B., Elegbede, A. I., Tobwala, S., Ganguly, B., Wagh, A. V., Muhonen, W. W., Law, B., Shabb, J. B., Srivastava, D. K., & Mallik, S. (2009). Release of liposomal contents by cell-secreted matrix metalloproteinase-9. Bioconjugate chemistry, 20(7), 1332–1339. https://doi.org/10.1021/bc9000646
1721. Khemtong, C., Kessinger, C. W., & Gao, J. (2009). Polymeric nanomedicine for cancer MR imaging and drug delivery. Chemical communications (Cambridge, England), (24), 3497–3510. https://doi.org/10.1039/b821865j
1722. Zupancich, J. A., Bates, F. S., & Hillmyer, M. A. (2009). Synthesis and self-assembly of RGD-functionalized PEO-PB amphiphiles. Biomacromolecules, 10(6), 1554–1563. https://doi.org/10.1021/bm900149b
1723. Zhao, W., & Karp, J. M. (2009). Tumour targeting: Nanoantennas heat up. Nature materials, 8(6), 453–454. https://doi.org/10.1038/nmat2463
1724. Vincent, A., Babu, S., Heckert, E., Dowding, J., Hirst, S. M., Inerbaev, T. M., Self, W. T., Reilly, C. M., Masunov, A. E., Rahman, T. S., & Seal, S. (2009). Protonated nanoparticle surface governing ligand tethering and cellular targeting. ACS nano, 3(5), 1203–1211. https://doi.org/10.1021/nn9000148
1725. Basu, S., Harfouche, R., Soni, S., Chimote, G., Mashelkar, R. A., & Sengupta, S. (2009). Nanoparticle-mediated targeting of MAPK signaling predisposes tumor to chemotherapy. Proceedings of the National Academy of Sciences of the United States of America, 106(19), 7957–7961. https://doi.org/10.1073/pnas.0902857106
1726. Wang, Z., Chui, W. K., & Ho, P. C. (2009). Design of a multifunctional PLGA nanoparticulate drug delivery system: evaluation of its physicochemical properties and anticancer activity to malignant cancer cells. Pharmaceutical research, 26(5), 1162–1171. https://doi.org/10.1007/s11095-009-9837-y
1727. Liu, J., Kopecková, P., Bühler, P., Wolf, P., Pan, H., Bauer, H., Elsässer-Beile, U., & Kopecek, J. (2009). Biorecognition and subcellular trafficking of HPMA copolymer-anti-PSMA antibody conjugates by prostate cancer cells. Molecular pharmaceutics, 6(3), 959–970. https://doi.org/10.1021/mp8002682
1728. Jin, S., & Labhasetwar, V. (2009). Nanotechnology in urology. The Urologic clinics of North America, 36(2), 179–viii. https://doi.org/10.1016/j.ucl.2009.02.005
1729. Agasti, S. S., Chompoosor, A., You, C. C., Ghosh, P., Kim, C. K., & Rotello, V. M. (2009). Photoregulated release of caged anticancer drugs from gold nanoparticles. Journal of the American Chemical Society, 131(16), 5728–5729. https://doi.org/10.1021/ja900591t
1730. Miller, A. C., Bershteyn, A., Tan, W., Hammond, P. T., Cohen, R. E., & Irvine, D. J. (2009). Block copolymer micelles as nanocontainers for controlled release of proteins from biocompatible oil phases. Biomacromolecules, 10(4), 732–741. https://doi.org/10.1021/bm800913r
1731. Siddiqui, I. A., Adhami, V. M., Bharali, D. J., Hafeez, B. B., Asim, M., Khwaja, S. I., Ahmad, N., Cui, H., Mousa, S. A., & Mukhtar, H. (2009). Introducing nanochemoprevention as a novel approach for cancer control: proof of principle with green tea polyphenol epigallocatechin-3-gallate. Cancer research, 69(5), 1712–1716. https://doi.org/10.1158/0008-5472.CAN-08-3978
1732. Kim, C. K., Ghosh, P., Pagliuca, C., Zhu, Z. J., Menichetti, S., & Rotello, V. M. (2009). Entrapment of hydrophobic drugs in nanoparticle monolayers with efficient release into cancer cells. Journal of the American Chemical Society, 131(4), 1360–1361. https://doi.org/10.1021/ja808137c
1733. Veiseh, O., Kievit, F. M., Gunn, J. W., Ratner, B. D., & Zhang, M. (2009). A ligand-mediated nanovector for targeted gene delivery and transfection in cancer cells. Biomaterials, 30(4), 649–657. https://doi.org/10.1016/j.biomaterials.2008.10.003
1734. Blanco, E., Kessinger, C. W., Sumer, B. D., & Gao, J. (2009). Multifunctional micellar nanomedicine for cancer therapy. Experimental biology and medicine (Maywood, N.J.), 234(2), 123–131. https://doi.org/10.3181/0808-MR-250
1735. Wu, W., Hsiao, S. C., Carrico, Z. M., & Francis, M. B. (2009). Genome-free viral capsids as multivalent carriers for taxol delivery. Angewandte Chemie (International ed. in English), 48(50), 9493–9497. https://doi.org/10.1002/anie.200902426
1736. Boomer, J. A., Qualls, M. M., Inerowicz, H. D., Haynes, R. H., Patri, V. S., Kim, J. M., & Thompson, D. H. (2009). Cytoplasmic delivery of liposomal contents mediated by an acid-labile cholesterol-vinyl ether-PEG conjugate. Bioconjugate chemistry, 20(1), 47–59. https://doi.org/10.1021/bc800239b
1737. Chen, B. A., Lai, B. B., Cheng, J., Xia, G. H., Gao, F., Xu, W. L., Ding, J. H., Gao, C., Sun, X. C., Xu, C. R., Chen, W. J., Chen, N. N., Liu, L. J., Li, X. M., & Wang, X. M. (2009). Daunorubicin-loaded magnetic nanoparticles of Fe3O4 overcome multidrug resistance and induce apoptosis of K562-n/VCR cells in vivo. International journal of nanomedicine, 4, 201–208. https://doi.org/10.2147/ijn.s7287
1738. Fang, C., & Zhang, M. (2009). Multifunctional Magnetic Nanoparticles for Medical Imaging Applications. Journal of materials chemistry, 19, 6258–6266. https://doi.org/10.1039/b902182e
1739. Zhu, Z. J., Ghosh, P. S., Miranda, O. R., Vachet, R. W., & Rotello, V. M. (2008). Multiplexed screening of cellular uptake of gold nanoparticles using laser desorption/ionization mass spectrometry. Journal of the American Chemical Society, 130(43), 14139–14143. https://doi.org/10.1021/ja805392f
1740. Mullen, D. G., Desai, A. M., Waddell, J. N., Cheng, X. M., Kelly, C. V., McNerny, D. Q., Majoros, I. J., Baker, J. R., Jr, Sander, L. M., Orr, B. G., & Banaszak Holl, M. M. (2008). The implications of stochastic synthesis for the conjugation of functional groups to nanoparticles. Bioconjugate chemistry, 19(9), 1748–1752. https://doi.org/10.1021/bc8002106
1741. Sun, C., Fang, C., Stephen, Z., Veiseh, O., Hansen, S., Lee, D., Ellenbogen, R. G., Olson, J., & Zhang, M. (2008). Tumor-targeted drug delivery and MRI contrast enhancement by chlorotoxin-conjugated iron oxide nanoparticles. Nanomedicine (London, England), 3(4), 495–505. https://doi.org/10.2217/17435889.3.4.495
1742. Wu, G., Mikhailovsky, A., Khant, H. A., Fu, C., Chiu, W., & Zasadzinski, J. A. (2008). Remotely triggered liposome release by near-infrared light absorption via hollow gold nanoshells. Journal of the American Chemical Society, 130(26), 8175–8177. https://doi.org/10.1021/ja802656d
1743. Pugno N. M. (2008). A new concept for smart drug delivery: adhesion induced nanovector implosion. The open medicinal chemistry journal, 2, 62–65. https://doi.org/10.2174/1874104500802010062
1744. Lee, D., Erigala, V. R., Dasari, M., Yu, J., Dickson, R. M., & Murthy, N. (2008). Detection of hydrogen peroxide with chemiluminescent micelles. International journal of nanomedicine, 3(4), 471–476.