Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis

dc.contributor.authorSakima, Vinicius Tatsuyuji [UNESP]
dc.contributor.authorBarbugli, Paula Aboud [UNESP]
dc.contributor.authorCerri, Paulo Sérgio [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorCarmello, Juliana Cabrini [UNESP]
dc.contributor.authorPavarina, Ana Cláudia [UNESP]
dc.contributor.authorDe Oliveira Mima, Ewerton Garcia [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:38:23Z
dc.date.available2018-12-11T17:38:23Z
dc.date.issued2018-08-19
dc.description.abstractAntimicrobial photodynamic therapy (aPDT) has been proposed as an alternative method for oral candidiasis (OC), while nanocarriers have been used to improve the water solubility of curcumin (CUR). The aim of this study is to encapsulate CUR in polymeric nanoparticles (NPs) and to evaluate its photodynamic effects on a murine model of OC. Anionic and cationic CUR-NP is synthesized using poly-lactic acid and dextran sulfate and then characterized. Female mice are immunosuppressed and inoculated with Candida albicans (Ca) to induce OC. aPDT is performed by applying CUR-NP or free CUR on the dorsum of the tongue, followed by blue light irradiation for five consecutive days. Nystatin is used as positive control. Afterward, Ca are recovered and cultivated. Animals are euthanized for histological, immunohistochemical, and DNA damage evaluation. Encapsulation in NP improves the water solubility of CUR. Nystatin shows the highest reduction of Ca, followed by aPDT mediated by free CUR, which results in immunolabelling of cytokeratins closer to those observed for healthy animals. Anionic CUR-NP does not show antifungal effect, and cationic CUR-NP reduces Ca even in the absence of light. DNA damage is associated with Ca infection. Consecutive aPDT application is a safe treatment for OC.en
dc.description.affiliationSchool of Dentistry São Paulo State University (UNESP)
dc.description.affiliationSchool of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.affiliationUnespSchool of Dentistry São Paulo State University (UNESP)
dc.description.affiliationUnespSchool of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.identifierhttp://dx.doi.org/10.3390/molecules23082075
dc.identifier.citationMolecules, v. 23, n. 8, 2018.
dc.identifier.doi10.3390/molecules23082075
dc.identifier.file2-s2.0-85052784415.pdf
dc.identifier.issn1420-3049
dc.identifier.lattes3278495911207882
dc.identifier.lattes1427125996716282
dc.identifier.orcid0000-0001-5756-5828
dc.identifier.scopus2-s2.0-85052784415
dc.identifier.urihttp://hdl.handle.net/11449/180152
dc.language.isoeng
dc.relation.ispartofMolecules
dc.relation.ispartofsjr0,855
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectCandida albicans
dc.subjectCurcumin
dc.subjectKeratins
dc.subjectMice
dc.subjectNanoparticles
dc.subjectOral candidiasis
dc.subjectPhotochemotherapy
dc.titleAntimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasisen
dc.typeArtigo
unesp.author.lattes3278495911207882[3]
unesp.author.lattes8867670539105403[6]
unesp.author.lattes1427125996716282
unesp.author.orcid0000-0001-5756-5828[3]
unesp.author.orcid0000-0002-9231-1994[6]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Odontologia, Araraquarapt
unesp.departmentFármacos e Medicamentos - FCFpt
unesp.departmentMateriais Odontológicos e Prótese - FOARpt
unesp.departmentMorfologia - FOARpt

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