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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...

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Autores principales: Singh, Neetu, Karambelkar, Amrita, Gu, Luo, Lin, Kevin, Miller, Jordan S., Chen, Christopher S., Sailor, Michael J., Bhatia, Sangeeta N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2011
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.
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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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