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hal.structure.identifierCentre de Recherche en Cancérologie Nantes-Angers [CRCNA]
hal.structure.identifierUniversité de Nantes [UN]
dc.contributor.authorGUEUGNON, Fabien
hal.structure.identifierCentre de Recherche en Cancérologie Nantes-Angers [CRCNA]
hal.structure.identifierUniversité de Nantes [UN]
dc.contributor.authorDENIS, Iza
hal.structure.identifierCentre de Recherche en Cancérologie Nantes-Angers [CRCNA]
hal.structure.identifierUniversité de Nantes [UN]
dc.contributor.authorPOULIQUEN, Daniel
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorCOLLETTE, Floraine
hal.structure.identifierInstitut de chimie des milieux et matériaux de Poitiers [UMR 7285] [IC2MP [Poitiers]]
dc.contributor.authorDELATOUCHE, Régis
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorHÉROGUEZ, Valérie
hal.structure.identifierCentre de Recherche en Cancérologie Nantes-Angers [CRCNA]
hal.structure.identifierUniversité de Nantes [UN]
dc.contributor.authorGREGOIRE, Marc
hal.structure.identifierInstitut de chimie des milieux et matériaux de Poitiers [UMR 7285] [IC2MP [Poitiers]]
dc.contributor.authorBERTRAND, Philippe
hal.structure.identifierCentre de Recherche en Cancérologie Nantes-Angers [CRCNA]
hal.structure.identifierUniversité de Nantes [UN]
dc.contributor.authorBLANQUART, Christophe
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2013
dc.identifier.issn1525-7797
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20403
dc.description.abstractEnWe described a norbornenyl-poly(ethylene oxide) nanoparticles ligand-free generic platform, made fluorescent with straightforward preparation by ring-opening metathesis polymerization (ROMP). Our method allowed to easily obtain a drug delivery system (DDS) with facilitated functionalization by means of azide-alkyne click chemistry and with a high selectivity for the tumor in vivo, while cellular internalization is obtained without cell targeting strategy. We demonstrated that our nanoparticles are internalized by endocytosis and colocalized with acidic intracellular compartments in two models of aggressive tumoral cell lines with low prognostic and limited therapeutic treatments. Our nanoparticles could be of real interest to limit the toxicity and to increase the clinical benefit of drugs suffering rapid clearance and side effects and an alternative for cancers with poorly efficient therapeutic solutions by associating the drug delivery in the tumor tissue with an acid-sensitive release system.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enPARTICLES
dc.subject.enIDENTIFICATION
dc.subject.enADENOCARCINOMA
dc.subject.enPOLYMERS
dc.subject.enROMP
dc.subject.enBLOCK-COPOLYMERS
dc.subject.enDRUG-DELIVERY
dc.subject.enCLICK CHEMISTRY
dc.subject.enMALIGNANT PLEURAL MESOTHELIOMA
dc.subject.enCELL
dc.title.enNanoparticles Produced by Ring-Opening Metathesis Polymerization Using Norbornenyl-poly(ethylene oxide) as a Ligand-Free Generic Platform for Highly Selective In Vivo Tumor Targeting
dc.typeArticle de revue
dc.identifier.doi10.1021/bm400516b
dc.subject.halChimie/Polymères
bordeaux.journalBiomacromolecules
bordeaux.page2396-2402
bordeaux.volume14
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue7
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00916100
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00916100v1
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