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Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin
[Image: see text] The platinum-based anticancer drugs cisplatin, carboplatin, and oxaliplatin are an important component of chemotherapy but are limited by severe dose-limiting side effects and the ability of tumors to develop resistance rapidly. These drugs can be improved through the use of drug-d...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662397/ https://www.ncbi.nlm.nih.gov/pubmed/20225865 http://dx.doi.org/10.1021/ja908117a |
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author | Brown, Sarah D. Nativo, Paola Smith, Jo-Ann Stirling, David Edwards, Paul R. Venugopal, Balaji Flint, David J. Plumb, Jane A. Graham, Duncan Wheate, Nial J. |
author_facet | Brown, Sarah D. Nativo, Paola Smith, Jo-Ann Stirling, David Edwards, Paul R. Venugopal, Balaji Flint, David J. Plumb, Jane A. Graham, Duncan Wheate, Nial J. |
author_sort | Brown, Sarah D. |
collection | PubMed |
description | [Image: see text] The platinum-based anticancer drugs cisplatin, carboplatin, and oxaliplatin are an important component of chemotherapy but are limited by severe dose-limiting side effects and the ability of tumors to develop resistance rapidly. These drugs can be improved through the use of drug-delivery vehicles that are able to target cancers passively or actively. In this study, we have tethered the active component of the anticancer drug oxaliplatin to a gold nanoparticle for improved drug delivery. Naked gold nanoparticles were functionalized with a thiolated poly(ethylene glycol) (PEG) monolayer capped with a carboxylate group. [Pt(1R,2R-diaminocyclohexane)(H(2)O)(2)]2NO(3) was added to the PEG surface to yield a supramolecular complex with 280 (±20) drug molecules per nanoparticle. The platinum-tethered nanoparticles were examined for cytotoxicity, drug uptake, and localization in the A549 lung epithelial cancer cell line and the colon cancer cell lines HCT116, HCT15, HT29, and RKO. The platinum-tethered nanoparticles demonstrated as good as, or significantly better, cytotoxicity than oxaliplatin alone in all of the cell lines and an unusual ability to penetrate the nucleus in the lung cancer cells. |
format | Online Article Text |
id | pubmed-3662397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-36623972013-05-24 Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin Brown, Sarah D. Nativo, Paola Smith, Jo-Ann Stirling, David Edwards, Paul R. Venugopal, Balaji Flint, David J. Plumb, Jane A. Graham, Duncan Wheate, Nial J. J Am Chem Soc [Image: see text] The platinum-based anticancer drugs cisplatin, carboplatin, and oxaliplatin are an important component of chemotherapy but are limited by severe dose-limiting side effects and the ability of tumors to develop resistance rapidly. These drugs can be improved through the use of drug-delivery vehicles that are able to target cancers passively or actively. In this study, we have tethered the active component of the anticancer drug oxaliplatin to a gold nanoparticle for improved drug delivery. Naked gold nanoparticles were functionalized with a thiolated poly(ethylene glycol) (PEG) monolayer capped with a carboxylate group. [Pt(1R,2R-diaminocyclohexane)(H(2)O)(2)]2NO(3) was added to the PEG surface to yield a supramolecular complex with 280 (±20) drug molecules per nanoparticle. The platinum-tethered nanoparticles were examined for cytotoxicity, drug uptake, and localization in the A549 lung epithelial cancer cell line and the colon cancer cell lines HCT116, HCT15, HT29, and RKO. The platinum-tethered nanoparticles demonstrated as good as, or significantly better, cytotoxicity than oxaliplatin alone in all of the cell lines and an unusual ability to penetrate the nucleus in the lung cancer cells. American Chemical Society 2010-03-12 2010-04-07 /pmc/articles/PMC3662397/ /pubmed/20225865 http://dx.doi.org/10.1021/ja908117a Text en Copyright © 2010 American Chemical Society |
spellingShingle | Brown, Sarah D. Nativo, Paola Smith, Jo-Ann Stirling, David Edwards, Paul R. Venugopal, Balaji Flint, David J. Plumb, Jane A. Graham, Duncan Wheate, Nial J. Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin |
title | Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin |
title_full | Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin |
title_fullStr | Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin |
title_full_unstemmed | Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin |
title_short | Gold Nanoparticles for the Improved Anticancer Drug Delivery of the Active Component of Oxaliplatin |
title_sort | gold nanoparticles for the improved anticancer drug delivery of the active component of oxaliplatin |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662397/ https://www.ncbi.nlm.nih.gov/pubmed/20225865 http://dx.doi.org/10.1021/ja908117a |
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