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Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release
[Image: see text] Mesoporous silica nanoparticles (MSNPs) have garnered a great deal of attention as potential carriers for therapeutic payloads. However, achieving triggered drug release from MSNPs in vivo has been challenging. Here, we describe the synthesis of stimulus-responsive polymer-coated M...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295203/ https://www.ncbi.nlm.nih.gov/pubmed/21981330 http://dx.doi.org/10.1021/ja206998x |
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author | Singh, Neetu Karambelkar, Amrita Gu, Luo Lin, Kevin Miller, Jordan S. Chen, Christopher S. Sailor, Michael J. Bhatia, Sangeeta N. |
author_facet | Singh, Neetu Karambelkar, Amrita Gu, Luo Lin, Kevin Miller, Jordan S. Chen, Christopher S. Sailor, Michael J. Bhatia, Sangeeta N. |
author_sort | Singh, Neetu |
collection | PubMed |
description | [Image: see text] Mesoporous silica nanoparticles (MSNPs) have garnered a great deal of attention as potential carriers for therapeutic payloads. However, achieving triggered drug release from MSNPs in vivo has been challenging. Here, we describe the synthesis of stimulus-responsive polymer-coated MSNPs and the loading of therapeutics into both the core and shell domains. We characterize MSNP drug-eluting properties in vitro and demonstrate that the polymer-coated MSNPs release doxorubicin in response to proteases present at a tumor site in vivo, resulting in cellular apoptosis. These results demonstrate the utility of polymer-coated nanoparticles in specifically delivering an antitumor payload. |
format | Online Article Text |
id | pubmed-3295203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-32952032012-03-06 Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release Singh, Neetu Karambelkar, Amrita Gu, Luo Lin, Kevin Miller, Jordan S. Chen, Christopher S. Sailor, Michael J. Bhatia, Sangeeta N. J Am Chem Soc [Image: see text] Mesoporous silica nanoparticles (MSNPs) have garnered a great deal of attention as potential carriers for therapeutic payloads. However, achieving triggered drug release from MSNPs in vivo has been challenging. Here, we describe the synthesis of stimulus-responsive polymer-coated MSNPs and the loading of therapeutics into both the core and shell domains. We characterize MSNP drug-eluting properties in vitro and demonstrate that the polymer-coated MSNPs release doxorubicin in response to proteases present at a tumor site in vivo, resulting in cellular apoptosis. These results demonstrate the utility of polymer-coated nanoparticles in specifically delivering an antitumor payload. American Chemical Society 2011-10-07 2011-12-14 /pmc/articles/PMC3295203/ /pubmed/21981330 http://dx.doi.org/10.1021/ja206998x Text en Copyright © 2011 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Singh, Neetu Karambelkar, Amrita Gu, Luo Lin, Kevin Miller, Jordan S. Chen, Christopher S. Sailor, Michael J. Bhatia, Sangeeta N. Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release |
title | Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release |
title_full | Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release |
title_fullStr | Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release |
title_full_unstemmed | Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release |
title_short | Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release |
title_sort | bioresponsive mesoporous silica nanoparticles for triggered drug release |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295203/ https://www.ncbi.nlm.nih.gov/pubmed/21981330 http://dx.doi.org/10.1021/ja206998x |
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