Bond strength and cytotoxicity of a universal adhesive according to the hybridization strategies to dentin

dc.contributor.authorLeite, Maria Luísa de Alencar e Silva [UNESP]
dc.contributor.authorCosta, Carlos Alberto de Souza [UNESP]
dc.contributor.authorDuarte, Rosângela Marques
dc.contributor.authorde Andrade, Ana Karina Maciel
dc.contributor.authorSoares, Diana Gabriela [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal da Paraíba (UFPB)
dc.date.accessioned2018-12-11T17:35:14Z
dc.date.available2018-12-11T17:35:14Z
dc.date.issued2018-01-01
dc.description.abstractThis study evaluated application protocol (etch-and-rinse/ER and self-etching/SE) and dentin wettability (wet and dry) on microtensile bond strength (µTBS) and transdentinal cytotoxicity of Scotchbond™ Universal (SU) adhesive system. The µTBS values and fracture mode were registered 24 h after adhesive system application and resin composite block build-up (n=5). For analysis of transdentinal cytotoxicity, odontoblast-like MDPC-23 cells were seeded on pulpal surface of dentin discs (0.4 mm thick) adapted to artificial pulp chambers (n=8). The adhesive system was applied to occlusal surface, followed by 24-h incubation time. Cell viability (Alamar Blue) and morphology (SEM) were assessed. Adper Single Bond 2 and Clearfil SE Bond were used as positive controls of the ER and SE application protocols, respectively. No treatment was performed on negative control (NC) group. Data were analyzed by ANOVA and Tukey’s tests (α=5%). Higher mTBS values were found for ER mode in comparison with SE protocol (p<0.05). Dentin wettability had no effect on bond strength of SU in both the ER and SE techniques (p>0.05). Most fractures involved hybrid layer and/or adhesive layer. Neither variable prevented the intense toxic effects of adhesive systems on MDPC-23 cultured cells, since intense reduction in cell viability (±88%) and severe alterations in cell morphology were observed for all groups compared to NC, with no differences among them (p>0.05). Therefore, it was concluded that application of SU following the ER protocol had better adhesive performance. However, this adhesive system featured intense transdentinal cytotoxicity to pulp cells, regardless of application protocol and dentin wettability.en
dc.description.affiliationDepartment of Dental Materials and Prosthodontics UNESP - Universidade Estadual Paulista
dc.description.affiliationDepartment of Physiology and Pathology UNESP - Universidade Estadual Paulista
dc.description.affiliationDepartment of Restorative Dentistry UFPB - Universidade Federal da Paraíba
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics UNESP - Universidade Estadual Paulista
dc.description.affiliationUnespDepartment of Physiology and Pathology UNESP - Universidade Estadual Paulista
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdCNPq: 303599/2014-6
dc.description.sponsorshipIdCNPq: 443153/2014-4
dc.format.extent68-75
dc.identifierhttp://dx.doi.org/10.1590/0103-6440201801698
dc.identifier.citationBrazilian Dental Journal, v. 29, n. 1, p. 68-75, 2018.
dc.identifier.doi10.1590/0103-6440201801698
dc.identifier.fileS0103-64402018000100068.pdf
dc.identifier.issn1806-4760
dc.identifier.issn0103-6440
dc.identifier.scieloS0103-64402018000100068
dc.identifier.scopus2-s2.0-85038423078
dc.identifier.urihttp://hdl.handle.net/11449/179447
dc.language.isoeng
dc.relation.ispartofBrazilian Dental Journal
dc.relation.ispartofsjr0,476
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectAdhesive system
dc.subjectBond strength
dc.subjectCytotoxicity
dc.subjectPulp cell
dc.titleBond strength and cytotoxicity of a universal adhesive according to the hybridization strategies to dentinen
dc.typeArtigo
unesp.author.lattes4517484241515548[2]
unesp.author.orcid0000-0002-7455-6867[2]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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