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Photodynamic antimicrobial therapy of curcumin in biofilms and carious dentine

dc.contributor.authorAraújo, N. C.
dc.contributor.authorFontana, Carla Raquel [UNESP]
dc.contributor.authorBagnato, V. S.
dc.contributor.authorGerbi, M. E M
dc.contributor.institutionFaculdade de Odontologia da Universidade de Pernambuco (UPE)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionLaser Center, Faculdade de Odontologia da Universidade de Pernambuco (UPE)
dc.date.accessioned2014-05-27T11:29:46Z
dc.date.available2014-05-27T11:29:46Z
dc.date.issued2013-06-24
dc.description.abstractPhotodynamic therapy (PDT) is a technique that involves the activation of photosensitizers by light in the presence of oxygen, resulting in the production of reactive radicals that are capable of inducing cell death. The present study evaluated the susceptibility of Streptococcus mutans and Lactobacillus acidophilus to PDT grown as multi-species in the biofilm phase versus in dentine carious lesions. A brain-heart infusion culture medium supplemented with 1 % glucose, 2 % sucrose, and 1 % young primary culture of L. acidophilus 108 CFU/mL and S. mutans 108 CFU/mL was used to develop multi-species biofilms and to induce caries on human dentine slabs. Five different concentrations of curcumin (0.75, 1.5, 3.0, 4.0, and 5.0 g/L) were used associated with 5.7 J/cm2 light emission diode. Four different groups were analyzed L-D- (control group), L-D+ (drug group), L+D- (light group), and L+D+ (PDT group). ANOVA/Tukey's tests were conducted to compare groups. A significant reduction (p <0.05) in cell viability was observed in the biofilm phase following photosensitization with all curcumin concentrations tested. To achieve significant bacterial reduction (p <0.05) in carious dentine, it was necessary to utilize 5.0 g/L of curcumin in association with blue light. No significant reduction was found for L-D+, supporting the absence of the drug's dark toxicity. S. mutans and L. acidophilus were susceptible to curcumin in the presence of blue light. However, due to light penetration and drug diffusion difficulties, these microorganisms within dentine carious lesions were less affected than they were in the biofilm phase. © 2013 Springer-Verlag London.en
dc.description.affiliationDepartamento de Dentística Faculdade de Odontologia da Universidade de Pernambuco (UPE), Av Gal Newton Cavalcanti 1650, Camaragibe, 54753-020
dc.description.affiliationDepartamento de Analises Clinicas, Faculdade de Ciências Farmacêuticas Univ Estadual Paulista (UNESP), Rua Expedicionários do Brasil 1621, Araraquara, 14801-960
dc.description.affiliationInstituto de Física de São Carlos Universidade de São Paulo (USP), Av Trabalhador São Carlense 400, São Carlos, 15980-900
dc.description.affiliationLaser Center, Faculdade de Odontologia da Universidade de Pernambuco (UPE), Av Gal Newton Cavalcanti 1650, Camaragibe, 54753-020
dc.description.affiliation, 154 Irmã Maria David Street, Recife, 52061-070
dc.description.affiliationUnespDepartamento de Analises Clinicas, Faculdade de Ciências Farmacêuticas Univ Estadual Paulista (UNESP), Rua Expedicionários do Brasil 1621, Araraquara, 14801-960
dc.format.extent1-7
dc.identifierhttp://dx.doi.org/10.1007/s10103-013-1369-3
dc.identifier.citationLasers in Medical Science, p. 1-7.
dc.identifier.doi10.1007/s10103-013-1369-3
dc.identifier.issn0268-8921
dc.identifier.issn1435-604X
dc.identifier.scopus2-s2.0-84879043808
dc.identifier.urihttp://hdl.handle.net/11449/75697
dc.identifier.wosWOS:000333051700030
dc.language.isoeng
dc.relation.ispartofLasers in Medical Science
dc.relation.ispartofjcr1.949
dc.relation.ispartofsjr0,713
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.subjectBiofilms
dc.subjectCariogenic bacteria
dc.subjectCurcumin
dc.subjectDentine
dc.subjectPhotodynamic therapy
dc.subjectStreptococcus mutans
dc.titlePhotodynamic antimicrobial therapy of curcumin in biofilms and carious dentineen
dc.typeArtigopt
dcterms.licensehttp://www.springer.com/open+access/authors+rights
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.lattes5168319315634298[2]
unesp.author.orcid0000-0002-9135-3690[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt

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