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dc.rights.licenseopen
hal.structure.identifierUniv Calif Los Angeles, Dept Bioengn
dc.contributor.authorLIAU, Walter T.
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorBONDUELLE, Colin
IDREF: 134527046
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorBROCHET, Marion
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLECOMMANDOUX, Sebastien
hal.structure.identifierUniv Calif Los Angeles, Dept Bioengn
dc.contributor.authorKASKO, Andrea M.
dc.date.accessioned2020
dc.date.available2020
dc.date.created2015
dc.date.issued2015
dc.identifier.issn1525-7797
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20262
dc.description.abstractEnBranched amphiphilic copolymers were synthesized through the reversible additionfragmentation chain transfer (RAFT) chain extension of a poly(methyl acrylate) macro-chain transfer agent using a protected galactose monomer and a polymerizable chain transfer agent branching unit. After galactose deprotection, the copolymers were self-assembled via nanoprecipitation. The resultant nanoparticles were analyzed for their size, shape, and biological interaction with a galactose binding lectin. Using light scattering, the nanoparticles were determined to be solid spheres. Nanoparticles containing branched glycoblocks bound significantly more lectin than those containing comparable linear blocks. By adjusting the molecular weight and branching of the copolymer, the size of the self-assembled nanoparticle and the saccharide density on its surface can be varied.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enPOLYMERS
dc.subject.enRECOGNITION
dc.subject.enPOLYSTYRENE
dc.subject.enLIVING RADICAL POLYMERIZATION
dc.subject.enBLOCK-COPOLYMERS
dc.subject.enDIBLOCK GLYCOPOLYMERS
dc.subject.enRAFT POLYMERIZATION
dc.subject.enBETA-CYCLODEXTRIN
dc.subject.enDRUG-DELIVERY
dc.subject.enMICELLES
dc.title.enSynthesis, Characterization, and Biological Interaction of Glyconanoparticles with Controlled Branching
dc.typeArticle de revue
dc.identifier.doi10.1021/bm501482q
dc.subject.halChimie/Polymères
bordeaux.journalBiomacromolecules
bordeaux.page284-294
bordeaux.volume16
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue1
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01361905
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01361905v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomacromolecules&rft.date=2015&rft.volume=16&rft.issue=1&rft.spage=284-294&rft.epage=284-294&rft.eissn=1525-7797&rft.issn=1525-7797&rft.au=LIAU,%20Walter%20T.&BONDUELLE,%20Colin&BROCHET,%20Marion&LECOMMANDOUX,%20Sebastien&KASKO,%20Andrea%20M.&rft.genre=article


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