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Susceptibility of Clinical Isolates of Candida to Photodynamic Effects of Curcumin

dc.contributor.authorDovigo, Livia N. [UNESP]
dc.contributor.authorPavarina, Ana C. [UNESP]
dc.contributor.authorCarmello, Juliana C. [UNESP]
dc.contributor.authorMachado, Ana L. [UNESP]
dc.contributor.authorBrunetti, Iguatemy Lourenço [UNESP]
dc.contributor.authorBagnato, Vanderlei S.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T13:47:19Z
dc.date.available2014-05-20T13:47:19Z
dc.date.issued2011-11-01
dc.description.abstractBackground and Objective: The resistance of Candida species to antifungals represents a major challenge for therapeutic and prophylactic strategies. This study evaluated photodynamic therapy (PDT) mediated by Curcumin (CUR) against clinical isolates of C. albicans, C. tropicalis, and C. glabrata, both in planktonic and biofilm forms. Study Design/Materials and Methods: Suspensions of Candida were treated with three CUR concentrations and exposed to four LED fluences. The protocol that showed the best outcomes for inactivation of the planktonic phase was selected to be evaluated against Candida biofilms. In addition, two higher CUR concentrations were tested. The metabolic activity of biofilms was evaluated by means of XTT reduction assay and the biofilm biomass was evaluated using crystal violet (CV) staining assay. Data were analyzed in a mixed model nested ANOVA, Wilcoxon's nonparametric tests, and the Kruskal-Wallis test (alpha = 5%). Results: The use of CUR in association with light was able to promote a significant antifungal effect against the planktonic form of the yeasts. When using 40 mu M of CUR, the metabolic activity of C. albicans, C. glabrata, and C. tropicalis biofilms was reduced by 85%, 85%, and 73%, respectively, at 18 J/cm(2). CUR-mediated PDT also decreased the biofilm biomass of all species evaluated. In addition, CV staining showed that C. albicans isolates were strong biofilm-forming strains, when compared with C. glabrata and C. tropicalis isolates. Conclusion: The results from the present investigation showed that low CUR concentrations can be highly effective for inactivating Candida isolates when associated with light excitation. Lasers Surg. Med. 43: 927-934, 2011. (C) 2011 Wiley Periodicals, Inc.en
dc.description.affiliationUniv Estadual Paulista UNESP, Araraquara Dent Sch, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUniv Estadual Paulista UNESP, Sch Pharmaceut Sci, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUniv São Paulo USP, Phys Inst São Carlos, BR-13566250 São Carlos, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Araraquara Dent Sch, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Sch Pharmaceut Sci, BR-14801902 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 08/03994-9
dc.description.sponsorshipIdFAPESP: 08/00601-6
dc.format.extent927-934
dc.identifierhttp://dx.doi.org/10.1002/lsm.21110
dc.identifier.citationLasers In Surgery and Medicine. Malden: Wiley-blackwell, v. 43, n. 9, p. 927-934, 2011.
dc.identifier.doi10.1002/lsm.21110
dc.identifier.issn0196-8092
dc.identifier.urihttp://hdl.handle.net/11449/16824
dc.identifier.wosWOS:000296460000010
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofLasers In Surgery and Medicine
dc.relation.ispartofjcr2.726
dc.relation.ispartofsjr0,926
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectCandida albicansen
dc.subjectCandida glabrataen
dc.subjectCandida tropicalisen
dc.subjectphotodynamic therapyen
dc.subjectturmericen
dc.titleSusceptibility of Clinical Isolates of Candida to Photodynamic Effects of Curcuminen
dc.typeArtigopt
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-blackwell
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes8867670539105403[2]
unesp.author.lattes8000248781842587[4]
unesp.author.orcid0000-0002-9231-1994[2]
unesp.author.orcid0000-0003-4927-7599[5]
unesp.author.orcid0000-0002-5435-7609[1]
unesp.author.orcid0000-0002-2718-428X[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt

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