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hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorGIACOMELLI, Cristiano
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorLE MEN, Lucile
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorBORSALI, Redouane
hal.structure.identifierImagerie Moléculaire et Nanobiotechnologies - Institut Européen de Chimie et Biologie [IECB]
dc.contributor.authorLAI-KEE-HIM, Josephine
hal.structure.identifierImagerie Moléculaire et Nanobiotechnologies - Institut Européen de Chimie et Biologie [IECB]
dc.contributor.authorBRISSON, Alain
hal.structure.identifierDepartment of Chemistry [Sheffield]
dc.contributor.authorARMES, Steven P.
hal.structure.identifierBiocompatibles UK Ltd
dc.contributor.authorLEWIS, A. L.
dc.date.accessioned2020
dc.date.available2020
dc.date.created2006
dc.date.issued2006
dc.identifier.issn1525-7797
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20759
dc.description.abstractEnThe micellization behavior of a diblock copolymer comprising a highly hydrophilic and biocompatible poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC corona-forming block and a pH-sensitive poly(2-(diisopropylamino)ethyl methacrylate) (PDPA) core-forming block (PMPC-b-PDPA) has been studied by static and dynamic light scattering (SDLS), transmission electron microscopy (TEM), and potentiometry. Self-assembly of PMPC-b-PDPA copolymers with two different DPA volume fractions (Phi DPA) leads to narrowly distributed and structurally distinct spherical micelles, as evidenced by their molecular weight (M-w,M-mic), aggregation number (N,(agg),,), hydrodynamic radius (RH), corona width (M, and core radius (R-c). The excellent potential of these pH-responsive micelles as nanosized drug delivery vehicles was illustrated by the encapsulation of dipyridamole (DIP), a model hydrophobic drug that dissolves in acid solutions and becomes insoluble above pH 5.8, which is comparable to the pK(a),, of the PDPA block. The influence of micelle structure (namely M-w,(mic), N (agg), RH, W, and R,) on drug loading content, drug loading efficiency, partition coefficient, and release kinetics was investigated and confirmed by fluorescence spectroscopy studies. The maximum dipyridamole loadings within PMPC30-b-PDPA(30) (RH = 14.0 nm; W = 4.8 nm; R-c = 9.2 nm) and PMPC30-b-PDPA(60) (RH = 27.1 nm; W = 11.0 nm; R, = 16.1 nm) tr:ticelles were 7 and 12% w/w(p), respectively. This preferential solubilization of DIP into micelles formed by copolymer chains having longer core-forming blocks (i.e., possessing larger core volumes) reflects the larger partition coefficient (K-v) of DIP between the aqueous phase and PMPC(30)b-PDPA(60) inicelles (Kv = 5.7 x 101) compared to PMPC30-b-PDPA(30) micelles (Kv = 1.1 x 10(4)). This enhanced ability Of PMPC30-b-PDPA(60) aggregates to entrap/stabilize small hydrophobic molecules also produces slower release kinetics. Rapid release can be triggered by lowering the pH to induce micellar dissociation.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enVESICLES
dc.subject.enMIXTURES
dc.subject.enMICELLIZATION
dc.subject.enPOLYMERS
dc.subject.enPOLYELECTROLYTES
dc.subject.enTRANSFER RADICAL POLYMERIZATION
dc.subject.enBIOCOMPATIBLE BLOCK-COPOLYMERS
dc.subject.enSOLUBILIZATION
dc.subject.enRELEASE
dc.subject.enPROBES
dc.title.enPhosphorylcholine-based pH-responsive diblock copolymer micelles as drug delivery vehicles: Light scattering, electron microscopy, and fluorescence experiments
dc.typeArticle de revue
dc.identifier.doi10.1021/bm0508921
dc.subject.halChimie/Polymères
bordeaux.journalBiomacromolecules
bordeaux.page817-828
bordeaux.volume7
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue3
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00342105
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00342105v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomacromolecules&rft.date=2006&rft.volume=7&rft.issue=3&rft.spage=817-828&rft.epage=817-828&rft.eissn=1525-7797&rft.issn=1525-7797&rft.au=GIACOMELLI,%20Cristiano&LE%20MEN,%20Lucile&BORSALI,%20Redouane&LAI-KEE-HIM,%20Josephine&BRISSON,%20Alain&rft.genre=article


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