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dc.rights.licenseembargoen_US
hal.structure.identifierQingdao University of Science and Technology
dc.contributor.authorWANG, Zhiwei
hal.structure.identifierQingdao University of Science and Technology
dc.contributor.authorLIN, Min
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.identifierQingdao University of Science and Technology
dc.contributor.authorLI, Rongye
hal.structure.identifierQingdao University of Science and Technology
dc.contributor.authorSHI, Zhekun
hal.structure.identifierLawrence Berkeley National Laboratory [Berkeley] [LBNL]
dc.contributor.authorZHU, Chenhui
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.identifierQingdao University of Science and Technology
dc.contributor.authorLI, Zhibo
hal.structure.identifierQingdao University of Science and Technology
dc.contributor.authorSUN, Jing
dc.date.accessioned2020-12-24T10:13:21Z
dc.date.available2020-12-24T10:13:21Z
dc.date.issued2020-07-28
dc.identifier.issn1526-4602en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/23598
dc.description.abstractEnDelicate control over architectures via crystallization-driven self-assembly (CDSA) in aqueous solution, particularly combined with external stimuli, is rare and challenging. Here, we report a stepwise CDSA process thermally initiated from amphiphilic poly(-allylglycine)-poly(-octylglycine) (PNAG--PNOG) conjugated with thiol-terminated triethylene glycol monomethyl ethers ((PNAG--EG)--PNOG) in aqueous solution. The diblock copolymers show a reversible thermoresponsive behavior with nearly identical cloud points in both heating and cooling runs. In contrast, the morphology transition of the assemblies is irreversible upon a heating-cooling cycle because of the presence of a confined domain arising from crystalline PNOG, which allows for the achievement of different nanostructured assemblies by the same polymer. We demonstrated that the thermoresponsive property of PNAG--EG initiates assembly kinetically that is subsequently promoted by crystallization of PNOG thermodynamically. The irreversible morphology transition behavior provides a convenient platform for comparing the cellular uptake efficiency of nanostructured assemblies with various morphologies that are otherwise similar.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subject.enMorphology
dc.subject.enCrystallization
dc.subject.enSolution chemistry
dc.subject.enCopolymers
dc.subject.enTransmission electron microscopy
dc.title.enThermoinduced Crystallization-Driven Self-Assembly of Bioinspired Block Copolymers in Aqueous Solution.
dc.title.alternativeBiomacromoleculesen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acs.biomac.0c00844en_US
dc.identifier.pubmed32786675en_US
bordeaux.journalBiomacromoleculesen_US
bordeaux.page3411-3419en_US
bordeaux.volume21en_US
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629en_US
bordeaux.issue8en_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.exportfalse
workflow.import.sourcepubmed
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomacromolecules&rft.date=2020-07-28&rft.volume=21&rft.issue=8&rft.spage=3411-3419&rft.epage=3411-3419&rft.eissn=1526-4602&rft.issn=1526-4602&rft.au=WANG,%20Zhiwei&LIN,%20Min&BONDUELLE,%20Colin&LI,%20Rongye&SHI,%20Zhekun&rft.genre=article


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