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dc.contributor.authorCheng, Hao
dc.contributor.authorKastrup, Christian
dc.contributor.authorRamanathan, Renuka
dc.contributor.authorSiegwart, Daniel J.
dc.contributor.authorMa, Minglin
dc.contributor.authorBogatyrev, Said R.
dc.contributor.authorBogatyrev, Said R.
dc.contributor.authorWhitehead, Kathryn A.
dc.contributor.authorLanger, Robert
dc.contributor.authorAnderson, Daniel G.
dc.date.accessioned2012-12-07T20:51:59Z
dc.date.available2012-12-07T20:51:59Z
dc.date.issued2010-02
dc.date.submitted2009-09
dc.identifier.issn1936-0851
dc.identifier.issn1936-086X
dc.identifier.urihttp://hdl.handle.net/1721.1/75301
dc.descriptionAuthor Manuscript: 2011 February 23.en_US
dc.description.abstractThe targeted delivery of therapeutics to tumors remains an important challenge in cancer nanomedicine. Attaching nanoparticles to cells that have tumoritropic migratory properties is a promising modality to address this challenge. Here we describe a technique to create nanoparticulate cellular patches that remain attached to the membrane of cells for up to 2 days. NeutrAvidin-coated nanoparticles were anchored on cells possessing biotinylated plasma membrane. Human bone marrow derived mesenchymal stem cells with nanoparticulate patches retained their inherent tumoritropic properties as shown using a tumor model in a 3D extracellular matrix. Additionally, human umbilical vein endothelial cells with nanoparticulate patches were able to retain their functional properties and form multicellular structures as rapidly as unmodified endothelial cells. These results provide a novel strategy to actively deliver nanostructures and therapeutics to tumors utilizing stem cells as carriers and also suggest that nanoparticulate cellular patches may have applications in tissue regeneration.en_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agency (Grant W911NF-07-1-0210)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant EB000244)en_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agency (Grant 2-P30- CA14051)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/nn901319yen_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.sourcePMCen_US
dc.titleNanoparticulate Cellular Patches for Cell-Mediated Tumoritropic Deliveryen_US
dc.typeArticleen_US
dc.identifier.citationCheng, Hao et al. “Nanoparticulate Cellular Patches for Cell-Mediated Tumoritropic Delivery.” ACS Nano 4.2 (2010): 625–631.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorRamanathan, Renuka
dc.relation.journalACS Nanoen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsCheng, Hao; Kastrup, Christian J.; Ramanathan, Renuka; Siegwart, Daniel J.; Ma, Minglin; Bogatyrev, Said R.; Xu, Qiaobing; Whitehead, Kathryn A.; Langer, Robert; Anderson, Daniel G.en
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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