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Susceptibility of Enterococcus faecalis and Propionibacterium acnes to antimicrobial photodynamic therapy

dc.contributor.authorde Annunzio, Sarah Raquel [UNESP]
dc.contributor.authorde Freitas, Laura Marise [UNESP]
dc.contributor.authorBlanco, Ana Lígia [UNESP]
dc.contributor.authorda Costa, Mardoqueu Martins
dc.contributor.authorCarmona-Vargas, Christian C.
dc.contributor.authorde Oliveira, Kleber Thiago
dc.contributor.authorFontana, Carla Raquel [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Brasil (UniBrasil)
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.date.accessioned2018-12-11T16:51:04Z
dc.date.available2018-12-11T16:51:04Z
dc.date.issued2018-01-01
dc.description.abstractBacterial resistance to available antibiotics nowadays is a global threat leading researchers around the world to study new treatment modalities for infections. Antimicrobial photodynamic therapy (aPDT) has been considered an effective and promising therapeutic alternative in this scenario. Briefly, this therapy is based on the activation of a non-toxic photosensitizing agent, known as photosensitizer (PS), by light at a specific wavelength generating cytotoxic singlet oxygen and free radicals. Virtually all studies related to aPDT involve a huge screening to identify ideal PS concentration and light dose combinations, a laborious and time-consuming process that is hardly disclosed in the literature. Herein, we describe an antimicrobial Photodynamic Therapy (aPDT) study against Enterococcus faecalis and Propionibacterium acnes employing methylene blue, chlorin-e6 or curcumin as PS. Similarities and discrepancies between the two bacterial species were pointed out in an attempt to speed up and facilitate futures studies against those clinical relevant strains. Susceptibility tests were performed by the broth microdilution method. Our results demonstrate that aPDT mediated by the three above-mentioned PS was effective in eliminating both gram-positive bacteria, although P. acnes showed remarkably higher susceptibility to aPDT when compared to E. faecalis. PS uptake assays revealed that P. acnes is 80 times more efficient than E. faecalis in internalizing all three PS molecules. Our results evidence that the cell wall structure is not a limiting feature when predicting bacterial susceptibility to aPDT treatment.en
dc.description.affiliationUniversidade Estadual Paulista (Unesp) Faculdade de Ciências Farmacêuticas Araraquara, Rodovia Araraquara-Jaú Km1, Campus Ville
dc.description.affiliationUniversidade Brasil (UniBrasil) Departamento de Engenharia Biomédica, Rua Carolina Fonseca, 235, Vila Santana
dc.description.affiliationUniversidade Federal de São Carlos (UFSCar) Departamento de Química Laboratório de Química Bioorgânica, Rodovia Washington Luis, Km 235 - SP-310
dc.description.affiliationUnespUniversidade Estadual Paulista (Unesp) Faculdade de Ciências Farmacêuticas Araraquara, Rodovia Araraquara-Jaú Km1, Campus Ville
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2016/05345-4
dc.format.extent545-550
dc.identifierhttp://dx.doi.org/10.1016/j.jphotobiol.2017.11.035
dc.identifier.citationJournal of Photochemistry and Photobiology B: Biology, v. 178, p. 545-550.
dc.identifier.doi10.1016/j.jphotobiol.2017.11.035
dc.identifier.file2-s2.0-85038883194.pdf
dc.identifier.issn1873-2682
dc.identifier.issn1011-1344
dc.identifier.scopus2-s2.0-85038883194
dc.identifier.urihttp://hdl.handle.net/11449/170499
dc.language.isoeng
dc.relation.ispartofJournal of Photochemistry and Photobiology B: Biology
dc.relation.ispartofsjr0,698
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAntimicrobial photodynamic therapy
dc.subjectChlorin-e6
dc.subjectCurcumin
dc.subjectEnterococcus faecalis
dc.subjectMethylene blue
dc.subjectPropionibacterium acnes
dc.titleSusceptibility of Enterococcus faecalis and Propionibacterium acnes to antimicrobial photodynamic therapyen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes5168319315634298[7]
unesp.author.orcid0000-0002-9722-0709[3]
unesp.author.orcid0000-0002-4395-3069[4]
unesp.author.orcid0000-0002-9135-3690[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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