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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorAGUT, Willy
hal.structure.identifierLaboratoire Léon Brillouin [LLB - UMR 12]
dc.contributor.authorBRÛLET, Annie
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorSCHATZ, Christophe
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorLECOMMANDOUX, Sebastien
dc.date.accessioned2020
dc.date.available2020
dc.date.created2010
dc.date.issued2010
dc.identifier.issn0743-7463
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20559
dc.description.abstractEnThe aqueous solution behavior of novel polypeptide-based double hydrophilic block copolymers (DHBCs), namely, poly[2-(dimethylamino)ethyl methacrylate]-b-poly(glutamic acid) (PDMAEMA-b-PGA), exhibiting pH- and temperature-responsiveness is presented using a combination of scattering techniques (light and neutron) and transmission electron microscopy. Close to the isoelectric point (IEP), direct or inverse electrostatic polymersomes are generated by electrostatic interactions developing between the two charged blocks and driving the formation of the hydrophobic membrane of the polymersomes, with the latter being stabilized in water by uncompensated charges. Under basic conditions, that is, when PDMAEMA is uncharged, the thermosensitivity of the DHBCs relates to the lower critical solution temperature (LCST) behavior of PDMAEMA around 40 degrees C. As a consequence, at pH = 11 and below this LCST, free chains of DHBC unimers are evidenced, while above the LCST the hydrophobicity of PDMAEMA drives the self-assembly of the DHBCs in a reversible manner. In this case, spherical polymeric micelles or polymersomes are obtained, depending on the PGA block length. These possibilities of variation in size and shape of morphologies that can be achieved as a function of temperature and/or pH variations open new routes in the development of multiresponsive nanocarriers for biomedical applications.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enCOACERVATE CORE MICELLES
dc.subject.enPOLYION COMPLEX MICELLES
dc.subject.enNEUTRON-SCATTERING
dc.subject.enAQUEOUS-SOLUTIONS
dc.subject.enGENE DELIVERY
dc.subject.enPOLY(2-VINYLPYRIDINIUM)-BLOCK-POLY(ETHYLENE OXIDE)
dc.subject.enCLICK CHEMISTRY
dc.subject.enDRUG-DELIVERY
dc.subject.enCROSS-LINKING
dc.subject.enPOLYPEPTIDE DIBLOCK COPOLYMERS
dc.title.enpH and Temperature Responsive Polymeric Micelles and Polymersomes by Self-Assembly of Poly[2-(dimethylamino)ethyl methacrylate]-b-Poly(glutamic acid) Double Hydrophilic Block Copolymers
dc.typeArticle de revue
dc.identifier.doi10.1021/la1005693
dc.subject.halChimie/Polymères
bordeaux.journalLangmuir
bordeaux.page10546-10554
bordeaux.volume26
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue13
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00652827
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00652827v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Langmuir&rft.date=2010&rft.volume=26&rft.issue=13&rft.spage=10546-10554&rft.epage=10546-10554&rft.eissn=0743-7463&rft.issn=0743-7463&rft.au=AGUT,%20Willy&BR%C3%9BLET,%20Annie&SCHATZ,%20Christophe&TATON,%20Daniel&LECOMMANDOUX,%20Sebastien&rft.genre=article


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