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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierInstitute of Nuclear Medicine and Allied Sciences
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorKAKKAR, Dipti
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorMAZZAFERRO, Silvia
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorTHEVENOT, Julie
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorSCHATZ, Christophe
hal.structure.identifierInstitute of Nuclear Medicine and Allied Sciences
dc.contributor.authorBHATT, Anant
hal.structure.identifierInstitute of Nuclear Medicine and Allied Sciences
dc.contributor.authorDWARAKANATH, Bilikere S.
hal.structure.identifierIndian Inst Technol, Ctr Biomed Engn
dc.contributor.authorSINGH, Harpal
hal.structure.identifierInstitute of Nuclear Medicine and Allied Sciences
dc.contributor.authorMISHRA, Anil K.
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLECOMMANDOUX, Sebastien
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2015
dc.identifier.issn1616-5187
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20278
dc.description.abstractEnHuisgen's 1,3-dipolar cycloaddition (Click Chemestry) has been used to prepare amphiphilic PEO-b-PBLG diblock and PBLG-b-PEO-b-PBLG triblock copolymers as potential carriers of anticancer drugs. Spherical and flower shaped micelles (D approximate to 100 nm) were obtained from diblock and triblock copolymers respectively. DOX was effectively encapsulated up to 18 wt.% and 50-60% of it was steadily released from the micelles over a period of 7 d. Flow cytometry and fluorescence microscopy confirmed the effective intracellular uptake as well as the sustained release of DOX from micelles. These results suggest that the diblock as well as triblock copolymers are promising carriers for intra-cellular drug delivery.
dc.language.isoen
dc.publisherWiley-VCH Verlag
dc.subject.enclick chemistry
dc.subject.enANTITUMOR-ACTIVITY
dc.subject.enINTRACELLULAR DELIVERY
dc.subject.enBIOMEDICAL APPLICATIONS
dc.subject.enTHERAPEUTIC APPLICATIONS
dc.subject.enblock-copolymers
dc.subject.enPOLY(ETHYLENE OXIDE)
dc.subject.enROD-COIL
dc.subject.enDRUG-DELIVERY
dc.subject.enPOLYMERIC MICELLES
dc.subject.enPOLY(GAMMA-BENZYL L-GLUTAMATE)
dc.subject.enPBLG
dc.subject.enPEO
dc.subject.enBLOCK-COPOLYMER
dc.subject.ennanoparticles
dc.title.enAmphiphilic PEO-b-PBLG Diblock and PBLG-b-PEO-b-PBLG Triblock Copolymer Based Nanoparticles: Doxorubicin Loading and In Vitro Evaluation
dc.typeArticle de revue
dc.identifier.doi10.1002/mabi.201400451
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecular Bioscience
bordeaux.page124-137
bordeaux.volume15
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue1
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01357683
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01357683v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Macromolecular%20Bioscience&rft.date=2015&rft.volume=15&rft.issue=1&rft.spage=124-137&rft.epage=124-137&rft.eissn=1616-5187&rft.issn=1616-5187&rft.au=KAKKAR,%20Dipti&MAZZAFERRO,%20Silvia&THEVENOT,%20Julie&SCHATZ,%20Christophe&BHATT,%20Anant&rft.genre=article


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