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Cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts
AIM: The purpose of this study was to investigate the cytotoxicity of nanohybrid mineral trioxide aggregate (MTA) in comparison with calcium-enriched mixture (CEM) cement and MTA-Angelus, using human gingival fibroblasts (HGFs). MATERIALS AND METHODS: Nine disc-shaped specimens of each material (in...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146766/ https://www.ncbi.nlm.nih.gov/pubmed/27994312 http://dx.doi.org/10.4103/0972-0707.194033 |
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author | Torshabi, Maryam Amid, Reza Kadkhodazadeh, Mahdi Shahrbabaki, Sara Eslami Tabatabaei, Fahimeh S. |
author_facet | Torshabi, Maryam Amid, Reza Kadkhodazadeh, Mahdi Shahrbabaki, Sara Eslami Tabatabaei, Fahimeh S. |
author_sort | Torshabi, Maryam |
collection | PubMed |
description | AIM: The purpose of this study was to investigate the cytotoxicity of nanohybrid mineral trioxide aggregate (MTA) in comparison with calcium-enriched mixture (CEM) cement and MTA-Angelus, using human gingival fibroblasts (HGFs). MATERIALS AND METHODS: Nine disc-shaped specimens of each material (in 2 set stat: A, set for 24 h; B, set for 30 min; and C, fresh stat) were prepared. HGFs were exposed to tested materials’ extracts or control media. Cytotoxicity testing was performed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide assay in two time intervals. STATISTICAL ANALYSIS: Results were evaluated by one-way ANOVA and t-test. Statistical significance was set at P < 0.05. RESULTS: CEM cement demonstrated favorable cell viability values when completely set (24 h set MTA = 24 h set CEM) at both time intervals. Interestingly, 24 h after incubation, CEM in Groups B and C demonstrated higher cell viability values than MTA (P < 0.05). However, after 72 h of incubation, these groups of CEM and MTA showed equal cell viability. All samples of nanohybrid MTA had slight cytotoxic effects after 24 h of incubation, and moderate cytotoxic effects after 72 h of incubation. CONCLUSION: Set CEM and set MTA-Angelus exerted similar, favorable effects on cell viability. However, within the limitations of this in vitro study, the results suggest that nanohybrid MTA could not be recommended as a material of choice for cervical root resorption. |
format | Online Article Text |
id | pubmed-5146766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51467662016-12-19 Cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts Torshabi, Maryam Amid, Reza Kadkhodazadeh, Mahdi Shahrbabaki, Sara Eslami Tabatabaei, Fahimeh S. J Conserv Dent Original Article AIM: The purpose of this study was to investigate the cytotoxicity of nanohybrid mineral trioxide aggregate (MTA) in comparison with calcium-enriched mixture (CEM) cement and MTA-Angelus, using human gingival fibroblasts (HGFs). MATERIALS AND METHODS: Nine disc-shaped specimens of each material (in 2 set stat: A, set for 24 h; B, set for 30 min; and C, fresh stat) were prepared. HGFs were exposed to tested materials’ extracts or control media. Cytotoxicity testing was performed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide assay in two time intervals. STATISTICAL ANALYSIS: Results were evaluated by one-way ANOVA and t-test. Statistical significance was set at P < 0.05. RESULTS: CEM cement demonstrated favorable cell viability values when completely set (24 h set MTA = 24 h set CEM) at both time intervals. Interestingly, 24 h after incubation, CEM in Groups B and C demonstrated higher cell viability values than MTA (P < 0.05). However, after 72 h of incubation, these groups of CEM and MTA showed equal cell viability. All samples of nanohybrid MTA had slight cytotoxic effects after 24 h of incubation, and moderate cytotoxic effects after 72 h of incubation. CONCLUSION: Set CEM and set MTA-Angelus exerted similar, favorable effects on cell viability. However, within the limitations of this in vitro study, the results suggest that nanohybrid MTA could not be recommended as a material of choice for cervical root resorption. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5146766/ /pubmed/27994312 http://dx.doi.org/10.4103/0972-0707.194033 Text en Copyright: © Journal of Conservative Dentistry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Torshabi, Maryam Amid, Reza Kadkhodazadeh, Mahdi Shahrbabaki, Sara Eslami Tabatabaei, Fahimeh S. Cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts |
title | Cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts |
title_full | Cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts |
title_fullStr | Cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts |
title_full_unstemmed | Cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts |
title_short | Cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts |
title_sort | cytotoxicity of two available mineral trioxide aggregate cements and a new formulation on human gingival fibroblasts |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146766/ https://www.ncbi.nlm.nih.gov/pubmed/27994312 http://dx.doi.org/10.4103/0972-0707.194033 |
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