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dc.contributor.authorSingh, Neetu
dc.contributor.authorKarambelkar, Amrita D.
dc.contributor.authorGu, Luo
dc.contributor.authorLin, Kevin Yu-Ming
dc.contributor.authorMiller, Jordan S.
dc.contributor.authorChen, Christopher S.
dc.contributor.authorSailor, Michael J.
dc.contributor.authorBhatia, Sangeeta N.
dc.date.accessioned2012-09-24T19:45:57Z
dc.date.available2012-09-24T19:45:57Z
dc.date.issued2011-11
dc.date.submitted2011-08
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/1721.1/73138
dc.description.abstractMesoporous 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.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (grant R01-CA124427)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (grant U54-CA119349)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (grant U54-CA119335)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ja206998xen_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceACSen_US
dc.titleBioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Releaseen_US
dc.typeArticleen_US
dc.identifier.citationSingh, Neetu et al. “Bioresponsive Mesoporous Silica Nanoparticles for Triggered Drug Release.” Journal of the American Chemical Society 133.49 (2011): 19582-19585. © 2011 American Chemical Societyen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.mitauthorSingh, Neetu
dc.contributor.mitauthorKarambelkar, Amrita D.
dc.contributor.mitauthorLin, Kevin Yu-Ming
dc.contributor.mitauthorBhatia, Sangeeta N.
dc.relation.journalJournal of the American Chemical Societyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSingh, Neetu; Karambelkar, Amrita; Gu, Luo; Lin, Kevin; Miller, Jordan S.; Chen, Christopher S.; Sailor, Michael J.; Bhatia, Sangeeta N.en
dc.identifier.orcidhttps://orcid.org/0000-0002-1293-2097
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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