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hal.structure.identifierLaboratory of Mammalian Cell Culture [GIGA-R]
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorLEGROS, Camille
hal.structure.identifierLaboratory of Mammalian Cell Culture [GIGA-R]
dc.contributor.authorDE PAUW-GILLET, Marie-Claire
hal.structure.identifierUniversity of Waterloo [Waterloo]
dc.contributor.authorTAM, Kam Chiu
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.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2013
dc.identifier.issn1759-9954
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20332
dc.description.abstractEnHydrogels and nanogels made from partially hydrolyzed poly(2-ethyl-2-oxazoline) (PEtOx) were prepared by two different processes. First, both hydrogels and nanogels were made in dilute media in the presence of 1,6-hexanediol di-glycidyl ether (1) as the cross-linker. Alternatively, the PEtOx precursor was engineered into nanogels by an inverse w/o emulsion process. In the latter case, in addition to cross-linker 1,a cleavable cross-linker homologue (2), namely 1,6-hydroxyethyl disulfide-bis-di-glycidyl ether, was used to produce cleavable nanogels. The pH-responsiveness of all cross-linked PEtOx derivatives was demonstrated in an acidic environment, owing to the protonation of residual ethylene imine groups and/or tertiary amines formed during the cross-linking reaction. Nanogels derived from cross-linker 2 could readily be cleaved under a reducing environment, due to the presence of disulfide linkages at the cross-linking points.
dc.language.isoen
dc.publisherRoyal Society of Chemistry - RSC
dc.subject.enPOLYMER
dc.subject.enPOLYOXAZOLINES
dc.subject.en2-METHYL-2-OXAZOLINE
dc.subject.enBLOCK-COPOLYMER MICELLES
dc.subject.enBIOMEDICAL APPLICATIONS
dc.subject.enNONIONIC HYDROGEL
dc.subject.enDRUG-DELIVERY
dc.subject.enPOLY(ETHYLENE GLYCOL)
dc.subject.enSENSITIVE HYDROGELS
dc.subject.enPOLY(2-OXAZOLINE)S
dc.title.enpH and redox responsive hydrogels and nanogels made from poly(2-ethyl-2-oxazoline)
dc.typeArticle de revue
dc.identifier.doi10.1039/c3py00685a
dc.subject.halChimie/Polymères
bordeaux.journalPolymer Chemistry
bordeaux.page4801-4808
bordeaux.volume4
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue17
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00959609
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00959609v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Polymer%20Chemistry&rft.date=2013&rft.volume=4&rft.issue=17&rft.spage=4801-4808&rft.epage=4801-4808&rft.eissn=1759-9954&rft.issn=1759-9954&rft.au=LEGROS,%20Camille&DE%20PAUW-GILLET,%20Marie-Claire&TAM,%20Kam%20Chiu&LECOMMANDOUX,%20Sebastien&TATON,%20Daniel&rft.genre=article


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