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dc.rights.licenseopenen_US
dc.contributor.authorBEN TRAD, Fatma
dc.contributor.authorWIECZNY, Vincent
dc.contributor.authorDELACOTTE, Jerome
dc.contributor.authorMOREL, Mathieu
dc.contributor.authorGUILLE-COLLIGNON, Manon
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorARBAULT, Stephane
dc.contributor.authorLEMAITRE, Frederic
dc.contributor.authorSOJIC, Neso
dc.contributor.authorLABBE, Eric
dc.contributor.authorBURIEZ, Olivier
dc.date.accessioned2024-11-14T12:03:31Z
dc.date.available2024-11-14T12:03:31Z
dc.date.issued2022-01-25
dc.identifier.issn0003-2700en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203263
dc.description.abstractEnIn this work, the characterization of release events from liposomes has been addressed quantitatively by an electrochemiluminescence (ECL) imaging strategy. First, ECL reagents ([Ru(bpy)3]2+ and tripropylamine) were encapsulated in sealed giant asymmetrical liposomes (100 μm in diameter) made of DOPG/DOPC phospholipids. After sedimentation on an indium tin oxide electrode material, the opening of liposomes was triggered by polarization of the surface. Under these conditions, amperometry, epifluorescence imaging, and ECL imaging were combined and synchronized to monitor and image the rupture of giant liposomes during the release and subsequent ECL emission of their redox content. Amperometry allowed the quantification of the content released from single liposomes. The location and status of liposomes (closed or opened) were assessed by epifluorescence imaging. ECL provided the image of the efflux of matter after liposome opening. This original ECL imaging approach favorably compares with strictly photoluminescent or electrochemical techniques and appears to be adapted for the investigation of membrane rupture/permeation events.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.title.enDynamic Electrochemiluminescence Imaging of Single Giant Liposome Opening at Polarized Electrodes
dc.title.alternativeAnal. Chem.en_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acs.analchem.1c04238en_US
dc.subject.halChimie/Matériauxen_US
bordeaux.journalAnalytical Chemistryen_US
bordeaux.page1686-1696en_US
bordeaux.volume94en_US
bordeaux.hal.laboratoriesCBMN : Chimie & de Biologie des Membranes & des Nano-objets - UMR 5248en_US
bordeaux.issue3en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDFondation de l'Ecole Normale Superieureen_US
bordeaux.identifier.funderIDSorbonne Universitéen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
dc.rights.ccCC BY-NC-NDen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Analytical%20Chemistry&rft.date=2022-01-25&rft.volume=94&rft.issue=3&rft.spage=1686-1696&rft.epage=1686-1696&rft.eissn=0003-2700&rft.issn=0003-2700&rft.au=BEN%20TRAD,%20Fatma&WIECZNY,%20Vincent&DELACOTTE,%20Jerome&MOREL,%20Mathieu&GUILLE-COLLIGNON,%20Manon&rft.genre=article


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