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dc.rights.licenseopenen_US
dc.contributor.authorLE GUERN, Florent
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorOUK, Tan-Sothea
dc.contributor.authorYERZHAN, Issabayev
dc.contributor.authorNURLYKYZ, Yesmurzayeva
dc.contributor.authorARNOUX, Philippe
dc.contributor.authorFROCHOT, Celine
dc.contributor.authorLEROY-LHEZ, Stephanie
dc.contributor.authorSOL, Vincent
dc.date.accessioned2021-07-09T07:19:37Z
dc.date.available2021-07-09T07:19:37Z
dc.date.issued2021
dc.identifier.otherhttps://www.mdpi.com/1420-3049/26/4/1122/s1en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/106480
dc.description.abstractEnDespite advances achieved over the last decade, infections caused by multi-drug-resistant bacterial strains are increasingly becoming important societal issues that need to be addressed. New approaches have already been developed in order to overcome this problem. Photodynamic antimicrobial chemotherapy (PACT) could provide an alternative to fight infectious bacteria. Many studies have highlighted the value of cationic photosensitizers in order to improve this approach. This study reports the synthesis and the characterization of cationic porphyrins derived from methylimidazolium and phenylimidazolium porphyrins, along with a comparison of their photophysical properties with the well-known N-methylpyridyl (pyridinium) porphyrin family. PACT tests conducted with the tetracationic porphyrins of these three families showed that these new photosensitizers may offer a good alternative to the classical pyridinium porphyrins, especially against S.aureus and E.coli. In addition, they pave the way to new cationic photosensitizers by the means of derivatization through amide bond formation.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enphotodynamic
dc.subject.entherapy
dc.subject.enantimicrobial
dc.subject.encationic
dc.subject.enporphyrin
dc.subject.enproperties
dc.subject.enphotophysical
dc.title.enPhotophysical and Bactericidal Properties of Pyridinium and Imidazolium Porphyrins for Photodynamic Antimicrobial Chemotherapy
dc.typeArticle de revueen_US
dc.identifier.doi10.3390/molecules26041122en_US
dc.subject.halChimie/Matériauxen_US
bordeaux.journalMoleculesen_US
bordeaux.page21. pen_US
bordeaux.volume26en_US
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248en_US
bordeaux.issue4en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03244508
hal.version1
hal.date.transferred2021-07-09T07:19:42Z
hal.exporttrue
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