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Viability and oxidative stress of dental pulp cells after indirect application of chemomechanical agents: An in vitro study

dc.contributor.authorLins-Candeiro, Caio Luiz
dc.contributor.authorParanhos, Luiz Renato
dc.contributor.authorde Oliveira Neto, Nilson Ferreira
dc.contributor.authorRibeiro, Rafael Antônio Oliveira [UNESP]
dc.contributor.authorde-Souza-Costa, Carlos Alberto [UNESP]
dc.contributor.authorGuedes, Fernanda Rodrigues
dc.contributor.authorda Silva, Washington Henrique Themoteo
dc.contributor.authorTurrioni, Ana Paula
dc.contributor.authorSantos Filho, Paulo César de Freitas
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T20:02:10Z
dc.date.issued2024-03-01
dc.description.abstractAim: This study evaluated the transdentinal cytotoxic effects of enzymatic agents (EA) for chemomechanical carious tissue removal on human dental pulp cells. Methodology: The groups were based on the performed dentine treatments (n = 8): G1: Positive Control (PC - no treatment); G2: Negative Control (NC - 35% H2O2 for 2 min); G3: Brix 3000™ (BX) for 30 s; G4: BX for 2 min; G5: Papacarie Duo™ (PD) for 30 s; G6: PD for 2 min. The cells were evaluated for viability (VB; MTT assay) and production of reactive oxygen species (ROS; DCFH-DA assay) and nitric oxide (NO; Griess reagent). A scanning electron microscope provided morphological chemical analyses and energy-dispersive X-ray spectroscopy. The data were submitted to the one-way anova statistical test complemented by Tukey (p <.05). Results: Cell viability decreased by 21.1% and 58.4% in G5 and G6, respectively. ROS production in G3 and G4 maintained basal levels but increased by 171.2% and 75.1% in G5 and G6, respectively. Conclusions: The Brix3000™ enzymatic agent did not cause indirect cytotoxic effects on pulp cells, regardless of the application time. Conversely, Papacarie Duo™ reduced viability and increased ROS production by pulp cells.en
dc.description.affiliationPost-graduation Program in Dentistry School of Dentistry Federal University of Uberlândia, Minas Gerais
dc.description.affiliationDivision of Preventive and Community Dentistry School of Dentistry Federal University of Uberlândia, Minas Gerais
dc.description.affiliationDepartment of Dental Materials and Prosthesis School of Dentistry São Paulo State University Júlio de Mesquita Filho, São Paulo
dc.description.affiliationDepartment of Physiology and Pathology School of Dentistry São Paulo State University Júlio de Mesquita Filho, São Paulo
dc.description.affiliationDivision of Pediatric Dentistry and Orthodontics School of Dentistry Federal University of Uberlândia, Minas Gerais
dc.description.affiliationDivision of Restorative Dentistry and Dental Materials School of Dentistry Federal University of Uberlândia, Minas Gerais
dc.description.affiliationUnespDepartment of Dental Materials and Prosthesis School of Dentistry São Paulo State University Júlio de Mesquita Filho, São Paulo
dc.description.affiliationUnespDepartment of Physiology and Pathology School of Dentistry São Paulo State University Júlio de Mesquita Filho, São Paulo
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.format.extent315-327
dc.identifierhttp://dx.doi.org/10.1111/iej.14013
dc.identifier.citationInternational Endodontic Journal, v. 57, n. 3, p. 315-327, 2024.
dc.identifier.doi10.1111/iej.14013
dc.identifier.issn1365-2591
dc.identifier.issn0143-2885
dc.identifier.scopus2-s2.0-85180000114
dc.identifier.urihttps://hdl.handle.net/11449/305153
dc.language.isoeng
dc.relation.ispartofInternational Endodontic Journal
dc.sourceScopus
dc.subjectcell survival
dc.subjectdental caries
dc.subjectdental materials
dc.subjectdental pulp
dc.subjectfree radicals
dc.titleViability and oxidative stress of dental pulp cells after indirect application of chemomechanical agents: An in vitro studyen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-7455-6867[5]
unesp.author.orcid0000-0002-6387-7411[8]

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