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dc.rights.licenseopenen_US
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorIBRAHIMOVA, Vusala
hal.structure.identifierUniversidad Autónoma de Madrid [UAM]
dc.contributor.authorGONZÁLEZ-DELGADO, José A
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLEVÊQUE, Manon
hal.structure.identifierInstituto IMDEA Nanociencia [Madrid]
hal.structure.identifierUniversidad Autónoma de Madrid [UAM]
dc.contributor.authorTORRES, Tomas
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorGARANGER, Elisabeth
IDREF: 089451740
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.accessioned2021-07-12T09:02:18Z
dc.date.available2021-07-12T09:02:18Z
dc.date.issued2021-07-09
dc.identifier.issn1520-4812en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/106520
dc.description.abstractEnStimuli-responsive recombinant elastin-like polypeptides (ELPs) are artificial protein polymers derived from the hydrophobic domain of tropoelastin that have attracted significant interest for drug delivery and tissue engineering applications. In the present study, we have conjugated a photosensitizer (PS) to a hydrophobic methionine-containing ELP scaffold, which upon reaction with singlet oxygen (O) is transformed into a hydrophilic sulfoxide derivative facilitating the disassembly of photosensitizer-delivery particles during the photodynamic therapy (PDT) process. A peripherally substituted carboxy-Zn(II)-phthalocyanine derivative (TT1) bearing a carboxyl group directly linked to the Pc-ring, and presenting an absorption maximum around 680 nm, was selected as PS which simultaneously acted as a photooxidation catalyst. A -ELP[MV-] conjugate was prepared from ELP[MV-] modified with an alkyne group at the -terminal chain end, and from TT1-amide-C3-azide by copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) reaction. This innovative model photooxidation sensitive PS delivery technology offers promising attributes in terms of temperature-controlled particle formation and oxidation-triggered release, narrow molar mass distribution, reproducibility, scalability, non-immunogenicity, biocompatibility, and biodegradability for pharmaceutical applications in an effort to improve the clinical effectiveness of PDT treatments.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.title.enPhotooxidation Responsive Elastin-Like Polypeptide Conjugates for Photodynamic Therapy Application
dc.title.alternativeBioconjug Chemen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acs.bioconjchem.1c00251en_US
dc.subject.halChimie/Polymèresen_US
dc.subject.halSciences du Vivant [q-bio]/Biochimie, Biologie Moléculaireen_US
dc.subject.halPhysique [physics]/Physique [physics]/Optique [physics.optics]en_US
dc.identifier.pubmed34240853en_US
dc.description.sponsorshipEuropeTemperature-responsive polypeptide nanocarriers for abdominal therapiesen_US
bordeaux.journalBioconjugate Chemistryen_US
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03283784
hal.version1
hal.date.transferred2021-07-12T09:02:22Z
hal.exporttrue
workflow.import.sourcepubmed
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