Artigo Produção Nacional Revisado por pares

The influence of methodology on the comparison of cytotoxicity of total-etch and self-etch adhesive systems

2022; Elsevier BV; Volume: 122; Linguagem: Inglês

10.1016/j.jdent.2022.104158

ISSN

1879-176X

Autores

Isleine Portal Caldas, Eduardo Moreira da Silva, Emanuelle Stellet Lourenço, Jean Carlos Martins do Nascimento, Paulo Emílio Corrêa Leite, Moira Pedroso Leão, Gutemberg Gomes Alves, Míriam Zaccaro Scelza,

Tópico(s)

Dental Research and COVID-19

Resumo

The present study aimed to compare the in vitro cytocompatibility of two etch-and-rinse (Adper Scothbond, Optibond) and two self-etch (Clearfill SE Bond and Single Bond Universal) dental adhesives through a dentin-barrier model with human pulp fibroblasts.Human fibroblasts were placed on a plastic device containing 500μm human dentin discs treated with each adhesive or without treatment (control). Other groups were directly exposed to media conditioned with adhesive samples according to ISO 10993-5:2009. After 24h exposure, cell viability was assessed by XTT, and released inflammatory mediators were detected with a multiparametric immunoassay.The standardized test without barrier indicated both etch-and-rinse adhesives and self-etch as cytotoxic, promoting viabilities under 70% of the control group (p<0.05). The dentin-barrier model identified increased cell viability for self-etch adhesives, with Clearfill SE Bond identified as non-cytotoxic. The immunoassay evidenced high rates of cytokines by cells exposed to the conditioned media of Adper Scotchbond, Optibond S, and Single Bond Universal.The use of a dentin-barrier in vitro model detected a better biocompatibility for self-etching adhesives and, in the case of Clearfill SE Bond, with a reversion from cytotoxic to biocompatible when compared to the indirect standardized test.The use of a dentin-barrier in vitro model was able to detect a better biocompatibility for self-etching adhesives when compared to the indirect standardized test and presents itself as a predictive in vitro method for assessing the cytotoxicity of dental restorative materials that may simulate the clinical condition more accurately.

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