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Toxicity of chlorhexidine on odontoblast-like cells

dc.contributor.authorLessa, Fernanda Campos Rosetti [UNESP]
dc.contributor.authorAranha, Andreza Maria Fabio [UNESP]
dc.contributor.authorNogueira, Indri [UNESP]
dc.contributor.authorGiro, Elisa Maria Aparecida [UNESP]
dc.contributor.authorHebling, Josimeri [UNESP]
dc.contributor.authorCosta, Carlos Alberto de Souza [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-04-28T21:00:55Z
dc.date.available2022-04-28T21:00:55Z
dc.date.issued2010-01-01
dc.description.abstractChlorhexidine gluconate (CHX) is recommended for a number of clinical procedures and it has been pointed out as a potential cavity cleanser to be applied before adhesive restoration of dental cavities. Objective: As CHX may diffuse through the dentinal tubules to reach a monolayer of odontoblasts that underlies the dentin substrate, this study evaluated the cytotoxic effects of different concentrations of CHX on cultured odontoblast-like cells (MDPC- 23). Material and Methods: Cells were cultured and exposed to CHX solutions at concentrations of 0.06%, 0.12%, 0.2%, 1% and 2%. Pure culture medium (α-MEM) and 3% hydrogen peroxide were used as negative and positive control, respectively. After exposing the cultured cells to the controls and CHX solutions for 60 s, 2 h or 60 s with a 24- h recovery period, cell metabolism (MTT assay) and total protein concentration were evaluated. Cell morphology was assessed under scanning electron microscopy. CHX had a dose-dependent toxic effect on the MDPC-23 cells. Results: Statistically significant difference was observed when the cells were exposed to CHX in all periods (p<0.05). Significant difference was also determined for all CHX concentrations (p<0.05). The 60-s exposure time was the least cytotoxic (p<0.05), while exposure to CHX for 60 s with a 24-h recovery period was the most toxic to the cells (p<0.05). Conclusion: Regardless of the exposure time, all CHX concentrations had a high direct cytotoxic effect to cultured MDPC-23 cells.en
dc.description.affiliationDiscipline of Pediatric Dentistry Department of Orthodontics and Pediatric Dentistry São Paulo State University Araraquara Dental School, Araraquara, SP
dc.description.affiliationDiscipline of Pathology Department of Physiology and Pathology São Paulo State University Araraquara Dental School, Araraquara, SP
dc.description.affiliationUnespDiscipline of Pediatric Dentistry Department of Orthodontics and Pediatric Dentistry São Paulo State University Araraquara Dental School, Araraquara, SP
dc.description.affiliationUnespDiscipline of Pathology Department of Physiology and Pathology São Paulo State University Araraquara Dental School, Araraquara, SP
dc.format.extent50-58
dc.identifierhttp://dx.doi.org/10.1590/S1678-77572010000100010
dc.identifier.citationJournal of Applied Oral Science, v. 18, n. 1, p. 50-58, 2010.
dc.identifier.doi10.1590/S1678-77572010000100010
dc.identifier.issn1678-7765
dc.identifier.issn1678-7757
dc.identifier.scopus2-s2.0-77950893606
dc.identifier.urihttp://hdl.handle.net/11449/225829
dc.language.isoeng
dc.relation.ispartofJournal of Applied Oral Science
dc.sourceScopus
dc.subjectCell viability
dc.subjectChlorhexidine
dc.subjectCytotoxicity
dc.subjectOdontoblasts
dc.subjectProtein synthesis
dc.titleToxicity of chlorhexidine on odontoblast-like cellsen
dc.typeArtigopt
dspace.entity.typePublication
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relation.isDepartmentOfPublication.latestForDiscoveryb3ba3d9c-022e-4521-8805-0bcceea7372e
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unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentClínica Infantil - FOARpt
unesp.departmentFisiologia e Patologia - FOARpt

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