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dc.contributor.authorElsabahy, Mahmoud
dc.contributor.authorZhang, Shiyi
dc.contributor.authorZhang, Fuwu
dc.contributor.authorDeng, Zhou J.
dc.contributor.authorLim, Young H.
dc.contributor.authorParsamian, Perouza
dc.contributor.authorWooley, Karen L.
dc.contributor.authorWang, Hai, Ph. D. Massachusetts Institute of Technology
dc.contributor.authorHammond, Paula T
dc.date.accessioned2014-02-19T15:36:47Z
dc.date.available2014-02-19T15:36:47Z
dc.date.issued2013-11
dc.date.submitted2013-09
dc.identifier.issn2045-2322
dc.identifier.urihttp://hdl.handle.net/1721.1/85001
dc.description.abstractThe construction of nanostructures from biodegradable precursors and shell/core crosslinking have been pursued as strategies to solve the problems of toxicity and limited stability, respectively. Polyphosphoester (PPE)-based micelles and crosslinked nanoparticles with non-ionic, anionic, cationic, and zwitterionic surface characteristics for potential packaging and delivery of therapeutic and diagnostic agents, were constructed using a quick and efficient synthetic strategy, and importantly, demonstrated remarkable differences in terms of cytotoxicity, immunotoxicity, and biofouling properties, as a function of their surface characteristics and also with dependence on crosslinking throughout the shell layers. For instance, crosslinking of zwitterionic micelles significantly reduced the immunotoxicity, as evidenced from the absence of secretions of any of the 23 measured cytokines from RAW 264.7 mouse macrophages treated with the nanoparticles. The micelles and their crosslinked analogs demonstrated lower cytotoxicity than several commercially-available vehicles, and their degradation products were not cytotoxic to cells at the range of the tested concentrations. PPE-nanoparticles are expected to have broad implications in clinical nanomedicine as alternative vehicles to those involved in several of the currently available medications.en_US
dc.description.sponsorshipNational Heart, Lung, and Blood Institute (Program of Excellence in Nanotechnology HHSN268201000046C)en_US
dc.description.sponsorshipNational Institute of Diabetes and Digestive and Kidney Diseases (U.S.) (R01-DK082546)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant DMR-0906815)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant DMR-1105304)en_US
dc.description.sponsorshipRobert A. Welch Foundation (W. T. Doherty-Welch Chair in Chemistry, Grant A-0001)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH P30 DC004665)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/srep03313en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/en_US
dc.sourceNature Publishing Groupen_US
dc.titleSurface Charges and Shell Crosslinks Each Play Significant Roles in Mediating Degradation, Biofouling, Cytotoxicity and Immunotoxicity for Polyphosphoester-based Nanoparticlesen_US
dc.typeArticleen_US
dc.identifier.citationElsabahy, Mahmoud, Shiyi Zhang, Fuwu Zhang, Zhou J. Deng, Young H. Lim, Hai Wang, Perouza Parsamian, Paula T. Hammond, and Karen L. Wooley. “Surface Charges and Shell Crosslinks Each Play Significant Roles in Mediating Degradation, Biofouling, Cytotoxicity and Immunotoxicity for Polyphosphoester-based Nanoparticles.” Scientific Reports 3 (November 22, 2013).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorZhang, Shiyien_US
dc.contributor.mitauthorDeng, Zhou J.en_US
dc.contributor.mitauthorHammond, Paula T.en_US
dc.relation.journalScientific Reportsen_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.orderedauthorsElsabahy, Mahmoud; Zhang, Shiyi; Zhang, Fuwu; Deng, Zhou J.; Lim, Young H.; Wang, Hai; Parsamian, Perouza; Hammond, Paula T.; Wooley, Karen L.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9688-2818
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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