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Photodynamic therapy of oral Candida infection in a mouse model

dc.contributor.authorFreire, Fernanda [UNESP]
dc.contributor.authorFerraresi, Cleber
dc.contributor.authorJorge, Antonio Olavo C. [UNESP]
dc.contributor.authorHamblin, Michael R.
dc.contributor.institutionMassachusetts General Hospital
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionHarvard Medical School
dc.contributor.institutionHarvard-MIT Division of Health Sciences and Technology
dc.date.accessioned2018-12-11T17:02:26Z
dc.date.available2018-12-11T17:02:26Z
dc.date.issued2016-06-01
dc.description.abstractSpecies of the fungal genus Candida, can cause oral candidiasis especially in immunosuppressed patients. Many studies have investigated the use of photodynamic therapy (PDT) to kill fungi in vitro, but this approach has seldom been reported in animal models of infection. This study investigated the effects of PDT on Candida albicans as biofilms grown in vitro and also in an immunosuppressed mouse model of oral candidiasis infection. We used a luciferase-expressing strain that allowed non-invasive monitoring of the infection by bioluminescence imaging. The phenothiazinium salts, methylene blue (MB) and new methylene blue (NMB) were used as photosensitizers (PS), combined or not with potassium iodide (KI), and red laser (660 nm) at four different light doses (10 J, 20 J, 40 J and 60 J). The best in vitro log reduction of CFU/ml on biofilm grown cells was: MB plus KI with 40 J (2.31 log; p < 0.001); and NMB without KI with 60 J (1.77 log; p < 0.001). These conditions were chosen for treating the in vivo model of oral Candida infection. After 5 days of treatment the disease was practically eradicated, especially using MB plus KI with 40 J. This study suggests that KI can potentiate PDT of fungal infection using MB (but not NMB) and could be a promising new approach for the treatment of oral candidiasis.en
dc.description.affiliationWellman Center for Photomedicine Massachusetts General Hospital
dc.description.affiliationDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology Universidade Estadual Paulista (UNESP) São José Dos Campos
dc.description.affiliationDepartment of Dermatology Harvard Medical School
dc.description.affiliationHarvard-MIT Division of Health Sciences and Technology
dc.description.affiliationUnespDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology Universidade Estadual Paulista (UNESP) São José Dos Campos
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2014/25772-9
dc.format.extent161-168
dc.identifierhttp://dx.doi.org/10.1016/j.jphotobiol.2016.03.049
dc.identifier.citationJournal of Photochemistry and Photobiology B: Biology, v. 159, p. 161-168.
dc.identifier.doi10.1016/j.jphotobiol.2016.03.049
dc.identifier.file2-s2.0-84963997652.pdf
dc.identifier.issn1873-2682
dc.identifier.issn1011-1344
dc.identifier.scopus2-s2.0-84963997652
dc.identifier.urihttp://hdl.handle.net/11449/172854
dc.language.isoeng
dc.relation.ispartofJournal of Photochemistry and Photobiology B: Biology
dc.relation.ispartofsjr0,698
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectAbbreviations PDT photodynamic therapy
dc.subjectKI potassium iodide
dc.subjectMB methylene blue
dc.subjectNMB new methylene blue
dc.subjectPS photosensitizers
dc.titlePhotodynamic therapy of oral Candida infection in a mouse modelen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes0053567153623569[3]
unesp.author.orcid0000-0002-1240-3988[1]
unesp.author.orcid0000-0001-6431-4605[4]
unesp.author.orcid0000-0002-1747-6158[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, São José dos Campospt
unesp.departmentBiociências e Diagnóstico Bucal - ICTpt

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