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Photodynamic Inactivation of Cariogenic Pathogens Using Curcumin as Photosensitizer

dc.contributor.authorAraújo, Natália Costa
dc.contributor.authorDe Menezes, Rebeca Ferraz
dc.contributor.authorCarneiro, Vanda Sanderana Macêdo
dc.contributor.authorDos Santos-Neto, Alexandrino Pereira
dc.contributor.authorFontana, Carla Raquel [UNESP]
dc.contributor.authorBagnato, Vanderlei Salvador
dc.contributor.authorHarvey, Catherine Malinda
dc.contributor.authorGerbi, Marleny Elizabeth Martinez
dc.contributor.institutionUniversity of Pernambuco (UPE)
dc.contributor.institutionDavis (UCDavis)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversity Center Tabosa de Almeida ASCES-UNITA
dc.date.accessioned2018-12-11T17:11:43Z
dc.date.available2018-12-11T17:11:43Z
dc.date.issued2017-05-01
dc.description.abstractObjective: This investigation assessed the susceptibility of Streptococcus mutans and Lactobacillus acidophilus to Photodynamic Therapy (PDT) when grown simultaneously in dentine carious lesions. Background data: PDT is a technique that utilizes light to activate photosensitizers in the presence of oxygen to produce reactive radicals. Materials and methods: A culture medium of 1% glucose, 2% sucrose, 1% young primary culture of L. acidophilus 108 CFU/mL, and S. mutans 108 CFU/mL was utilized to inoculate the bacterial induced caries on human dentine slabs. Different concentrations of the photosensitizer (0.75, 1.5, 3.0, 4.0, and 5.0 g/L) were activated through exposure to the light-emitting diode source with a central wavelength of 450 nm and a fluency of 5.7 J/cm2. Two light intensities (19 and 47.5 mW/cm2) were tested. Four different groups were analyzed: L-D- (control group), L-D+ (drug group), L+D+1 (PDT group 1, light intensity of 19 mW/cm2), and L+D+2 (PDT group 2, light intensity of 47.5 mW/cm2). ANOVA/Tukey tests were utilized to compare groups (α = 5%). Results: Both light intensities required 5.0 g/L of curcumin for significant bacterial reduction (p < 0.05). No significant effect was found for L-D+, thus proving the absence of a potential inherent toxicity. Conclusions: Curcumin has a toxic effect on microorganisms at appreciable concentrations upon photoactivation. However, it was required to use the maximum concentration of the drug for a successful procedure.en
dc.description.affiliationDepartment of Restorative Dentistry Dental School of Pernambuco University of Pernambuco (UPE), 1650 Gal Newton Cavalcanti Avenue
dc.description.affiliationDepartment of Endodontics University of Pernambuco (UPE)
dc.description.affiliationCenter for Biophotonics University of California Davis (UCDavis)
dc.description.affiliationDepartment of Clinical Analysis School of Pharmaceutical Sciences Universidade Estadual Paulista (UNESP)
dc.description.affiliationOptics Group Physics Institute of São Carlos (IFSC) University of São Paulo (USP)
dc.description.affiliationLaser Center University of Pernambuco (UPE)
dc.description.affiliationFaculty of Dentistry University Center Tabosa de Almeida ASCES-UNITA
dc.description.affiliationUnespDepartment of Clinical Analysis School of Pharmaceutical Sciences Universidade Estadual Paulista (UNESP)
dc.format.extent259-263
dc.identifierhttp://dx.doi.org/10.1089/pho.2016.4156
dc.identifier.citationPhotomedicine and Laser Surgery, v. 35, n. 5, p. 259-263, 2017.
dc.identifier.doi10.1089/pho.2016.4156
dc.identifier.file2-s2.0-85019061624.pdf
dc.identifier.issn1549-5418
dc.identifier.scopus2-s2.0-85019061624
dc.identifier.urihttp://hdl.handle.net/11449/174558
dc.language.isoeng
dc.relation.ispartofPhotomedicine and Laser Surgery
dc.relation.ispartofsjr0,443
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectdentin
dc.subjectdentistry
dc.subjectphotodynamic therapy
dc.titlePhotodynamic Inactivation of Cariogenic Pathogens Using Curcumin as Photosensitizeren
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
unesp.author.lattes5168319315634298[5]
unesp.author.orcid0000-0002-9135-3690[5]
unesp.departmentAnálises Clínicas - FCFpt

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