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Liquid crystal precursor system as a vehicle for curcumin-mediated photodynamic inactivation of oral biofilms

dc.contributor.authorReina, Bárbara Donadon [UNESP]
dc.contributor.authorSantezi, Carolina
dc.contributor.authorMalheiros, Samuel Santana [UNESP]
dc.contributor.authorCalixto, Giovana
dc.contributor.authorRodero, Camila [UNESP]
dc.contributor.authorVictorelli, Francesca Damiani [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorDovigo, Lívia Nordi [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionIndependent Researcher at the Moment of the Submission (Unaffiliated Researcher)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2023-07-29T13:24:42Z
dc.date.available2023-07-29T13:24:42Z
dc.date.issued2023-02-01
dc.description.abstractCurcumin has great potential as a photosensitizer, but it has low solubility in aqueous solutions. This study reports the antimicrobial efficacy of photodynamic inactivation (PDI) mediated by a curcumin-loaded liquid crystal precursor (LCP) on in situ dental biofilms. Thirty volunteers used intraoral devices containing enamel samples for 48 hours for biofilm formation. The samples were then removed from the device and treated either with LCP with 160 μM of curcumin plus illumination at 18 J/cm2 (C + L+ group) or with LCP without curcumin in the dark (C – L − group). Following this, the biofilm from the samples was plated for quantifying the viable colonies at 37°C for 48 hours. Specific and nonspecific media were used for the presumptive isolation of Streptococcus mutans, Lactobacillus species/aciduric microorganisms, Candida species, and total microbiota. The C + L+ group showed a highly significant (P <.001) reduction in the log10 (colony forming units/mL) values as compared to the C − L − group for all culture media. Hierarchical linear regression indicated that there may be predictors at individual volunteer level explaining the difference in the PDI efficacy among different individuals (P =.001). The LCP system retained curcumin and released it slowly and continuously, thus protecting the drug from photodegradation. LCP with curcumin is considered effective for the photoinactivation of dental biofilms, but the PDI efficacy may differ based on the host's individual characteristics.en
dc.description.affiliationDepartment of Social Dentistry School of Dentistry–São Paulo State University (UNESP)
dc.description.affiliationIndependent Researcher at the Moment of the Submission (Unaffiliated Researcher)
dc.description.affiliationDepartment of Biosciences Piracicaba Dental School - University of Campinas (UNICAMP)
dc.description.affiliationDepartment of Drugs and Medicines School of Pharmaceutical Sciences - São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Social Dentistry School of Dentistry–São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Drugs and Medicines School of Pharmaceutical Sciences - São Paulo State University (UNESP)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2015/24112-8
dc.description.sponsorshipIdFAPESP: 2016/24918-5
dc.identifierhttp://dx.doi.org/10.1002/jbio.202200040
dc.identifier.citationJournal of Biophotonics, v. 16, n. 2, 2023.
dc.identifier.doi10.1002/jbio.202200040
dc.identifier.issn1864-0648
dc.identifier.issn1864-063X
dc.identifier.scopus2-s2.0-85139979059
dc.identifier.urihttp://hdl.handle.net/11449/247747
dc.language.isoeng
dc.relation.ispartofJournal of Biophotonics
dc.sourceScopus
dc.subjectcurcumin
dc.subjectdental plaque
dc.subjectliquid crystal
dc.subjectphotochemotherapy
dc.titleLiquid crystal precursor system as a vehicle for curcumin-mediated photodynamic inactivation of oral biofilmsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.author.orcid0000-0003-1041-5835[4]
unesp.author.orcid0000-0002-6698-0545[7]
unesp.author.orcid0000-0002-5435-7609[8]
unesp.departmentFármacos e Medicamentos - FCFpt

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