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dc.rights.licenseopenen_US
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
hal.structure.identifierCentre de Recherche Paul Pascal [CRPP]
dc.contributor.authorFAUQUIGNON, Martin
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorSOLBERG, Amalie
hal.structure.identifierInstitut Laue-Langevin [ILL]
dc.contributor.authorPORCAR, Lionel
hal.structure.identifierCentre de Recherche Paul Pascal [CRPP]
dc.contributor.authorCHAPEL, Jean-Paul
hal.structure.identifierNorwegian University of Science and Technology [NTNU]
dc.contributor.authorCHRISTENSEN, Bjørn E
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorSCHATZ, Christophe
dc.date.accessioned2024-10-06T08:34:30Z
dc.date.available2024-10-06T08:34:30Z
dc.date.issued2024-10-01
dc.identifier.issn1526-4602en_US
dc.identifier.otherhttps://doi.ill.fr/10.5291/ILL-DATA.9-11-2032en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202268
dc.description.abstractEnAlginates are marine polysaccharides known for their ability to selectively bind calcium ions and form hydrogels. They are widely used in biomedical applications but are challenging to produce as nanogels. Here we introduce a self-assembly route to create stable alginate-based nanogels under near-equilibrium conditions. Guluronate (G) blocks, which interact with divalent cations such as Ca, Ba, and Sr, were extracted from alginates and covalently linked through their reducing end to the reducing end of dextran (Dex) chains, forming linear block copolymers that self-assemble into micellar nanogels with a core-corona structure in the presence of these ions. Real-time dynamic light scattering (DLS) and small-angle neutron scattering (SANS) were used to study the self-assembly mechanism of the copolymer during dialysis against divalent ions. For the G--Dex copolymer, we achieved spherical micelles with an 8 nm radius and an aggregation number of around 20. Although the type of divalent cation affected micelle stability, it did not influence their size. Micellar nanogels are dynamic structures, capable of ion exchange, and can disassemble with chelating agents like ethylenediamine tetraacetic acid (EDTA).
dc.description.sponsorshipAuto-Assemblage de bicouches de copolymères amphiphiles induit par une surface - ANR-18-CE06-0016en_US
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.title.enMicellar Nanogels from Alginate-Based Diblock Copolysaccharides
dc.title.alternativeBiomacromoleculesen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acs.biomac.4c00717en_US
dc.subject.halChimie/Polymèresen_US
dc.identifier.pubmed39351822en_US
bordeaux.journalBiomacromoleculesen_US
bordeaux.pageDOI: 10.1021/acs.biomac.4c00717en_US
bordeaux.volume25en_US
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629en_US
bordeaux.hal.laboratoriesCentre de Recherche Paul Pascal (CRPP) - UMR 5031en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04722785
hal.version1
hal.date.transferred2024-10-06T08:34:35Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccCC BY-NC-SAen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomacromolecules&rft.date=2024-10-01&rft.volume=25&rft.spage=DOI:%2010.1021/acs.biomac.4c00717&rft.epage=DOI:%2010.1021/acs.biomac.4c00717&rft.eissn=1526-4602&rft.issn=1526-4602&rft.au=FAUQUIGNON,%20Martin&SOLBERG,%20Amalie&PORCAR,%20Lionel&CHAPEL,%20Jean-Paul&CHRISTENSEN,%20Bj%C3%B8rn%20E&rft.genre=article


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