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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorHOUGA, Clément
hal.structure.identifierCentre de recherches Paul Pascal [CRPP]
dc.contributor.authorGIERMANSKA, Joanna
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.identifierCentre de Recherches sur les Macromolécules Végétales [CERMAV]
hal.structure.identifierUniversité Joseph Fourier - Grenoble 1 [UJF]
dc.contributor.authorBORSALI, Redouane
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorGNANOU, Yves
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLE MEINS, Jean-Francois
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2009
dc.identifier.issn1525-7797
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20736
dc.description.abstractEnThe self-assembly of dextran-block-polystyrene (dex-b-PS) block copolymers was investigated in solution. The hydrophobic PS weight fraction in these block copolymers ranges from 7 to 92% w/w, whereas the average number molar mass of dextran was kept constant at 6600 gmol(-1). Self-assembly by direct dissolution in water could be performed only for block copolymers with a low hydrophobic content (7% w/w), whereas mixtures of tetrahydrofuran and dimethylsulfoxide were required for higher PS content, before transferring the structures into water. Core-shell micelles, ovoids, and vesicles could be identified upon characterization by light and neutrons scattering, atomic force microscopy, and transmission electron microscopy. Most of the morphologies observed were not expected considering the chemical composition of the block copolymers. Finally, the size and shape of these nanoparticles were fixed upon cross-linking the dextran block through reaction of the hydroxyl groups with divinylsulfone. The role of the dextran conformation on the self-assembly process is discussed.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enblock copolymers
dc.subject.enself-assembly
dc.subject.enmicelles
dc.subject.envesicles
dc.subject.endextran
dc.subject.enpolysaccharide
dc.title.enMicelles and Polymersomes Obtained by Self-Assembly of Dextran and Polystyrene Based Block Copolymers
dc.typeArticle de revue
dc.identifier.doi10.1021/bm800778n
dc.subject.halChimie/Polymères
bordeaux.journalBiomacromolecules
bordeaux.page32-40
bordeaux.volume10
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue1
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00358603
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00358603v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomacromolecules&rft.date=2009&rft.volume=10&rft.issue=1&rft.spage=32-40&rft.epage=32-40&rft.eissn=1525-7797&rft.issn=1525-7797&rft.au=HOUGA,%20Cl%C3%A9ment&GIERMANSKA,%20Joanna&LECOMMANDOUX,%20Sebastien&BORSALI,%20Redouane&TATON,%20Daniel&rft.genre=article


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