Publicação:
Curcumin-mediated photodynamic inactivation of Candida albicans in a murine model of oral candidiasis

dc.contributor.authorDovigo, Lívia Nordi
dc.contributor.authorCarmello, Juliana Cabrini
dc.contributor.authorDe Souza Costa, Carlos Alberto
dc.contributor.authorVergani, Carlos Eduardo [UNESP]
dc.contributor.authorBrunetti, Iguatemy Lourenço [UNESP]
dc.contributor.authorBagnato, Vanderlei Salvador
dc.contributor.authorPavarina, Ana Cláudia
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-27T11:28:48Z
dc.date.available2014-05-27T11:28:48Z
dc.date.issued2013-04-01
dc.description.abstractIn vitro investigations of curcumin-mediated photodynamic therapy (PDT) are encouraging, but there is a lack of reliable in vivo evidence of its efficacy. This study describes the photoinactivation of Candida albicans in a murine model of oral candidiasis, using curcumin as a photosensitizer. Forty immunosuppressed mice were orally inoculated with C. albicans and after five days, they received topical curcumin (20, 40 and 80 μM) and illumination with LED light. The use of curcumin or light alone were also investigated. Positive control animals did not receive any treatment and negative control animals were not inoculated with C. albicans. The number of surviving yeast cells was determined and analyzed by ANOVA and Tukey's post-hoc test (α = 0.05). Histological evaluation of the presence of yeast and inflammatory reaction was also conducted. All exposures to curcumin with LED light caused a significant reduction in C. albicans viability after PDT, but the use of 80 μM curcumin associated with light was able to induce the highest log10 reduction in colony counts (4 logs). It was concluded that curcumin-mediated PDT proved to be effective for in vivo inactivation of C. albicans without harming the host tissue of mice. © 2013 ISHAM.en
dc.description.affiliationDepartments of Social Dentistry Araraquara Dental School, Araraquara, São Paulo
dc.description.affiliationDepartments of Dental Materials and Prosthodontics Araraquara Dental School, Araraquara, São Paulo
dc.description.affiliationDepartments of Physiology and Pathology Araraquara Dental School, Araraquara, São Paulo
dc.description.affiliationSchool of Pharmaceutics Sciences UNESP-Univ Estadual Paulista, Araraquara, São Paulo
dc.description.affiliationBiophotonics Lab Group of Optics, Physics Institute of São Carlos University of São Paulo-USP, São Carlos, São Paulo
dc.description.affiliationUnespSchool of Pharmaceutics Sciences UNESP-Univ Estadual Paulista, Araraquara, São Paulo
dc.format.extent243-251
dc.identifierhttp://dx.doi.org/10.3109/13693786.2012.714081
dc.identifier.citationMedical Mycology, v. 51, n. 3, p. 243-251, 2013.
dc.identifier.doi10.3109/13693786.2012.714081
dc.identifier.issn1369-3786
dc.identifier.issn1460-2709
dc.identifier.lattes0127570480681342
dc.identifier.orcid0000-0002-7375-4714
dc.identifier.scopus2-s2.0-84875137461
dc.identifier.urihttp://hdl.handle.net/11449/75027
dc.identifier.wosWOS:000316228100003
dc.language.isoeng
dc.relation.ispartofMedical Mycology
dc.relation.ispartofjcr2.799
dc.relation.ispartofsjr0,973
dc.relation.ispartofsjr0,973
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectCandida infection
dc.subjectCurcumin
dc.subjectLED
dc.subjectPhotodynamic therapy
dc.subjectcurcumin
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectCandida albicans
dc.subjectcontrolled study
dc.subjectfemale
dc.subjecthistopathology
dc.subjectinflammation
dc.subjectmouse
dc.subjectnonhuman
dc.subjectphotodynamic therapy
dc.subjectthrush
dc.subjectyeast cell
dc.titleCurcumin-mediated photodynamic inactivation of Candida albicans in a murine model of oral candidiasisen
dc.typeArtigo
dcterms.licensehttp://informahealthcare.com/userimages/ContentEditor/1255620309227/Copyright_And_Permissions.pdf
dspace.entity.typePublication
unesp.author.lattes0127570480681342
unesp.author.lattes8867670539105403[7]
unesp.author.lattes4517484241515548[3]
unesp.author.lattes3003130522427820[4]
unesp.author.orcid0000-0002-7375-4714[4]
unesp.author.orcid0000-0002-9231-1994[7]
unesp.author.orcid0000-0002-7455-6867[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt

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