Tài liệu tham khảo |
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Chi tiết |
1. Ferrari M., Cancer nanotechnology: opportunities and challenges. Nat. Rev. Cancer, 2005. 5: p. 161-171 |
Sách, tạp chí |
Tiêu đề: |
Cancer nanotechnology: opportunities and challenges |
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2. Cuenca A.G., Jing H., Hochwald S.N., Delano M., Cance W.G., Grobmyer S. and R., Emerging implications of nanotechnology on cancer diagnostics and therapeutics. Cancer, 2006. 107: p. 459-466 |
Sách, tạp chí |
Tiêu đề: |
Emerging implications of nanotechnology on cancer diagnostics and therapeutics |
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3. Moghimi S.M., Hunter A.C., Murray J.C., Long-circulating and target-specific nanoparticles: Theory to practice. Pharmacol. ReV, 2001. 53: p. 283–318 |
Sách, tạp chí |
Tiêu đề: |
Long-circulating and target-specific nanoparticles: Theory to practice |
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5. Torchilin V.P., et al., Multifunctional nanocarriers. Adv Drug Deliv Rev, 2006. 58(14): p. 1532-1555 |
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Tiêu đề: |
Multifunctional nanocarriers |
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6. Nasongkla N., Bey E., Ren J.M. et al., Multifunctional polymeric micelles as cancer-targeted, MRI-ultrasensitive drug delivery systems. Nano Lett, 2006.6(11): p. 2427-2430 |
Sách, tạp chí |
Tiêu đề: |
Multifunctional polymeric micelles as cancer-targeted, MRI-ultrasensitive drug delivery systems |
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8. Yang J., Lee C.H., Park J. et al., Antibody conjugated magnetic PLGA nanoparticles for diagnosis and treatment of breast cancer. J Mater Chem, 2007.17(26): p. 2695-2705 |
Sách, tạp chí |
Tiêu đề: |
Antibody conjugated magnetic PLGA nanoparticles for diagnosis and treatment of breast cancer |
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9. Liu J., Lee H., Allen C., Formulation of drugs in block copolymer micelles: drug loading and release. Curr Pharm Des, 2006. 12(36): p. 4685-4701 |
Sách, tạp chí |
Tiêu đề: |
Formulation of drugs in block copolymer micelles: drug loading and release |
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10. Takaichi W., Yui S., Tetsuya I., Yukitaka K., Tsutomu O., Indocyanine green- laden poly(ethylene glycol)-block-polylactide (PEG-b-PLA) nanocapsules incorporating reverse micelles: Effects of PEG-b-PLA composition on the nanocapsule diameter and encapsulation efficiency. Colloids and Surfaces A, 2017. 520: p. 764-770 |
Sách, tạp chí |
Tiêu đề: |
Indocyanine green-laden poly(ethylene glycol)-block-polylactide (PEG-b-PLA) nanocapsules incorporating reverse micelles: Effects of PEG-b-PLA composition on the nanocapsule diameter and encapsulation efficiency |
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11. Owens D.E., Peppas N.A., Opsonization, biodistribution, and pharmacokinetics of polymeric nanoparticles. Int. J. Pharm, 2006. 307: p. 93–102 |
Sách, tạp chí |
Tiêu đề: |
Opsonization, biodistribution, and pharmacokinetics of polymeric nanoparticles |
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12. Romberg B., Hennink W.E., Storm G., Sheddable coatings for long-circulating nanoparticles. Pharm. Res, 2008. 25: p. 55–71 |
Sách, tạp chí |
Tiêu đề: |
Sheddable coatings for long-circulating nanoparticles |
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13. Bartlett D.W., Su H., Hildebrandt I.J., Weber W.A., Davis M.E., Impact of tumor- specific targeting on the biodistribution and efficacy of siRNA nanoparticles measured by multimodality in vivo imaging. Proc. Natl. Acad. Sci, 2007. 104: p.15549–15554 |
Sách, tạp chí |
Tiêu đề: |
Impact of tumor-specific targeting on the biodistribution and efficacy of siRNA nanoparticles measured by multimodality in vivo imaging |
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14. Hainfeld J.F., Slatkin D.N., Focella T.M. et al., Gold nanoparticles: a new X-ray contrast agent. Br J Radiol, 2006. 79(93): p. 248-253 |
Sách, tạp chí |
Tiêu đề: |
Gold nanoparticles: a new X-ray contrast agent |
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15. Bulte J.W.M., Kraichman D.L., Iron oxide MR contrast agents for molecular and cellular imaging. Nmr Biomed, 2004. 17(7): p. 484-499 |
Sách, tạp chí |
Tiêu đề: |
Iron oxide MR contrast agents for molecular and cellular imaging |
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16. Otsuka H., Nagasaki Y., Kataoka K., PEGylated nanoparticles for biological and pharmaceutical applications. Adv Drug Deliv Rev, 2003. 55: p. 403-19 |
Sách, tạp chí |
Tiêu đề: |
PEGylated nanoparticles for biological and pharmaceutical applications |
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17. Wang S., L.Y., Zhou J., Wang M., Wang Y., PLA-PEG-FA NPs for drug delivery system: Evaluation of carrier micro-structure, degradation and size-cell proliferation relationship. Materials Science and Engineering: C, 2018. 91: p. 297- 302 |
Sách, tạp chí |
Tiêu đề: |
PLA-PEG-FA NPs for drug delivery system: Evaluation of carrier micro-structure, degradation and size-cell proliferation relationship |
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18. Nagayama S., O.K., Fukuoka Y., Higaki K., Kimura T., Time-dependent changes in opsonin amount associated on nanoparticles alter their hepatic uptake characteristics. Int. J. Pharm, 2007. 342: p. 215–221 |
Sách, tạp chí |
Tiêu đề: |
Time-dependent changes in opsonin amount associated on nanoparticles alter their hepatic uptake characteristics |
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19. Kandasamy V., Mariappan R., Mechanism for the Nano-Based Drug Delivery System. Characterization and Biology of Nanomaterials for Drug Delivery, 2018:p. 219-263 |
Sách, tạp chí |
Tiêu đề: |
Mechanism for the Nano-Based Drug Delivery System |
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20. Beletsi A., Panagi Z., Avgoustakis K., Biodistribution properties of nanoparticles based on mixtures of PLGA with PLGA PEG diblock copolymers. Int. J. Pharm, 2005. 298: p. 233–241 |
Sách, tạp chí |
Tiêu đề: |
Biodistribution properties of nanoparticles based on mixtures of PLGA with PLGA PEG diblock copolymers |
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21. Nagesha D.K., Plouffe B.D., Phan M., Lewis L.H., Sridhar S., Murthy S.K., Functionalization-induced improvement in magnetic pproperties of Fe3O4 nanoparticles for biomedical applications. J. Applied Physics, 2009. 105 |
Sách, tạp chí |
Tiêu đề: |
Functionalization-induced improvement in magnetic pproperties of Fe3O4 nanoparticles for biomedical applications |
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22. Purushtham S., Ramanujan R.V., Thermoresponsive magnetic composite nanomaterials for multimodal cancer therapy. Acta Biomaterialia, 2010. 6: p. 502- 510 |
Sách, tạp chí |
Tiêu đề: |
Thermoresponsive magnetic composite nanomaterials for multimodal cancer therapy |
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