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Bioresponsive mesoporous silica nanoparticles for triggered drug release.


ABSTRACT: 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.

SUBMITTER: Singh N 

PROVIDER: S-EPMC3295203 | biostudies-literature | 2011 Dec

REPOSITORIES: biostudies-literature

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Bioresponsive mesoporous silica nanoparticles for triggered drug release.

Singh Neetu N   Karambelkar Amrita A   Gu Luo L   Lin Kevin K   Miller Jordan S JS   Chen Christopher S CS   Sailor Michael J MJ   Bhatia Sangeeta N SN  

Journal of the American Chemical Society 20111118 49


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 protease  ...[more]

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