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Cytotoxicity of Etch-and-Rinse, Self-Etch, and Universal Dental Adhesive Systems in Fibroblast Cell Line 3T3
The aim of this study was to evaluate in fibroblast cultures the direct cytotoxic effects of etch-and-rinse, self-etch, and universal adhesive systems. The sterile glass cover slips (n = 3) were then immersed in culture medium to obtain the eluates for the experimental groups: (1) Adper™ Single Bond...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662068/ https://www.ncbi.nlm.nih.gov/pubmed/29109829 http://dx.doi.org/10.1155/2017/9650420 |
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author | Pupo, Yasmine Mendes Bernardo, Cintia Fernanda de Freitas de Souza, Francielly Fernanda de Freitas A. Michél, Milton Domingos Ribeiro, Camila Nunes de Morais Germano, Sandro Maluf, Daniela Florencio |
author_facet | Pupo, Yasmine Mendes Bernardo, Cintia Fernanda de Freitas de Souza, Francielly Fernanda de Freitas A. Michél, Milton Domingos Ribeiro, Camila Nunes de Morais Germano, Sandro Maluf, Daniela Florencio |
author_sort | Pupo, Yasmine Mendes |
collection | PubMed |
description | The aim of this study was to evaluate in fibroblast cultures the direct cytotoxic effects of etch-and-rinse, self-etch, and universal adhesive systems. The sterile glass cover slips (n = 3) were then immersed in culture medium to obtain the eluates for the experimental groups: (1) Adper™ Single Bond 2; (2) Ambar; (3) Adper™ Scotchbond™ Multi-Purpose; (4) Scotchbond™ Universal; (5) Ambar Universal; and (6) OptiBond All-In-One. As a negative control, sterile glass cover slips were immersed in culture medium only. After 24 h, the eluate obtained was applied on fibroblast culture. Cell viability and cell morphology were evaluated by MTT assay and SEM, respectively. Data were analyzed by Kruskal–Wallis and Mann–Whitney tests (α = 0.05). All adhesive systems except universal reduced cell viability in 3T3 cells to between 26.04% and 56.57%, and Scotchbond Universal and Ambar Universal reduced cell viability to 2.13% and 3.57%, respectively, when compared to the negative control. Cytoplasmic membrane shrinkage and cell-free areas with residual membrane fragments from dead cells were observed. In conclusion, improvements in universal adhesive system formulations and their mechanisms of action are not accompanied by increased toxicity compared with those in other systems, warranting commitment to the use of these dentin-pulp complexes. |
format | Online Article Text |
id | pubmed-5662068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-56620682017-11-06 Cytotoxicity of Etch-and-Rinse, Self-Etch, and Universal Dental Adhesive Systems in Fibroblast Cell Line 3T3 Pupo, Yasmine Mendes Bernardo, Cintia Fernanda de Freitas de Souza, Francielly Fernanda de Freitas A. Michél, Milton Domingos Ribeiro, Camila Nunes de Morais Germano, Sandro Maluf, Daniela Florencio Scanning Research Article The aim of this study was to evaluate in fibroblast cultures the direct cytotoxic effects of etch-and-rinse, self-etch, and universal adhesive systems. The sterile glass cover slips (n = 3) were then immersed in culture medium to obtain the eluates for the experimental groups: (1) Adper™ Single Bond 2; (2) Ambar; (3) Adper™ Scotchbond™ Multi-Purpose; (4) Scotchbond™ Universal; (5) Ambar Universal; and (6) OptiBond All-In-One. As a negative control, sterile glass cover slips were immersed in culture medium only. After 24 h, the eluate obtained was applied on fibroblast culture. Cell viability and cell morphology were evaluated by MTT assay and SEM, respectively. Data were analyzed by Kruskal–Wallis and Mann–Whitney tests (α = 0.05). All adhesive systems except universal reduced cell viability in 3T3 cells to between 26.04% and 56.57%, and Scotchbond Universal and Ambar Universal reduced cell viability to 2.13% and 3.57%, respectively, when compared to the negative control. Cytoplasmic membrane shrinkage and cell-free areas with residual membrane fragments from dead cells were observed. In conclusion, improvements in universal adhesive system formulations and their mechanisms of action are not accompanied by increased toxicity compared with those in other systems, warranting commitment to the use of these dentin-pulp complexes. Hindawi Publishing Corporation 2017-01-10 /pmc/articles/PMC5662068/ /pubmed/29109829 http://dx.doi.org/10.1155/2017/9650420 Text en Copyright © 2017 Yasmine Mendes Pupo et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Pupo, Yasmine Mendes Bernardo, Cintia Fernanda de Freitas de Souza, Francielly Fernanda de Freitas A. Michél, Milton Domingos Ribeiro, Camila Nunes de Morais Germano, Sandro Maluf, Daniela Florencio Cytotoxicity of Etch-and-Rinse, Self-Etch, and Universal Dental Adhesive Systems in Fibroblast Cell Line 3T3 |
title | Cytotoxicity of Etch-and-Rinse, Self-Etch, and Universal Dental Adhesive Systems in Fibroblast Cell Line 3T3 |
title_full | Cytotoxicity of Etch-and-Rinse, Self-Etch, and Universal Dental Adhesive Systems in Fibroblast Cell Line 3T3 |
title_fullStr | Cytotoxicity of Etch-and-Rinse, Self-Etch, and Universal Dental Adhesive Systems in Fibroblast Cell Line 3T3 |
title_full_unstemmed | Cytotoxicity of Etch-and-Rinse, Self-Etch, and Universal Dental Adhesive Systems in Fibroblast Cell Line 3T3 |
title_short | Cytotoxicity of Etch-and-Rinse, Self-Etch, and Universal Dental Adhesive Systems in Fibroblast Cell Line 3T3 |
title_sort | cytotoxicity of etch-and-rinse, self-etch, and universal dental adhesive systems in fibroblast cell line 3t3 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662068/ https://www.ncbi.nlm.nih.gov/pubmed/29109829 http://dx.doi.org/10.1155/2017/9650420 |
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