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Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study

This in vitro study evaluated the effect of myristyltrimethylammonium bromide (MYTAB) on the physical, chemical, and biological properties of an experimental dental resin. The resin was formulated with dental dimetacrylate monomers and a photoinitiator/co-initiator system. MYTAB was added at 0.5 (G(...

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Autores principales: Mena Silva, Paola Andrea, Garcia, Isadora Martini, Nunes, Julia, Visioli, Fernanda, Castelo Branco Leitune, Vicente, Melo, Mary Anne, Collares, Fabrício Mezzomo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151596/
https://www.ncbi.nlm.nih.gov/pubmed/32075267
http://dx.doi.org/10.3390/jfb11010009
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author Mena Silva, Paola Andrea
Garcia, Isadora Martini
Nunes, Julia
Visioli, Fernanda
Castelo Branco Leitune, Vicente
Melo, Mary Anne
Collares, Fabrício Mezzomo
author_facet Mena Silva, Paola Andrea
Garcia, Isadora Martini
Nunes, Julia
Visioli, Fernanda
Castelo Branco Leitune, Vicente
Melo, Mary Anne
Collares, Fabrício Mezzomo
author_sort Mena Silva, Paola Andrea
collection PubMed
description This in vitro study evaluated the effect of myristyltrimethylammonium bromide (MYTAB) on the physical, chemical, and biological properties of an experimental dental resin. The resin was formulated with dental dimetacrylate monomers and a photoinitiator/co-initiator system. MYTAB was added at 0.5 (G(0.5%)), 1 (G(1%)), and 2 (G(2%)) wt %, and one group remained without MYTAB and was used as the control (G(Ctrl)). The resins were analyzed for the polymerization kinetics, degree of conversion, ultimate tensile strength (UTS), antibacterial activity against Streptococcus mutans, and cytotoxicity against human keratinocytes. Changes in the polymerization kinetics profiling were observed, and the degree of conversion ranged from 57.36% (±2.50%) for G(2%) to 61.88% (±1.91%) for G(0.5%), without a statistically significant difference among groups (p > 0.05). The UTS values ranged from 32.85 (±6.08) MPa for G(0.5%) to 35.12 (±5.74) MPa for G(Ctrl) (p > 0.05). MYTAB groups showed antibacterial activity against biofilm formation from 0.5 wt % (p < 0.05) and against planktonic bacteria from 1 wt % (p < 0.05). The higher the MYTAB concentration, the higher the cytotoxic effect, without differences between G(Ctrl) e G(0.5%) (p > 0.05). In conclusion, the addition of 0.5 wt % of MYTAB did not alter the physical and chemical properties of the dental resin and provided antibacterial activity without cytotoxic effect.
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spelling pubmed-71515962020-04-20 Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study Mena Silva, Paola Andrea Garcia, Isadora Martini Nunes, Julia Visioli, Fernanda Castelo Branco Leitune, Vicente Melo, Mary Anne Collares, Fabrício Mezzomo J Funct Biomater Article This in vitro study evaluated the effect of myristyltrimethylammonium bromide (MYTAB) on the physical, chemical, and biological properties of an experimental dental resin. The resin was formulated with dental dimetacrylate monomers and a photoinitiator/co-initiator system. MYTAB was added at 0.5 (G(0.5%)), 1 (G(1%)), and 2 (G(2%)) wt %, and one group remained without MYTAB and was used as the control (G(Ctrl)). The resins were analyzed for the polymerization kinetics, degree of conversion, ultimate tensile strength (UTS), antibacterial activity against Streptococcus mutans, and cytotoxicity against human keratinocytes. Changes in the polymerization kinetics profiling were observed, and the degree of conversion ranged from 57.36% (±2.50%) for G(2%) to 61.88% (±1.91%) for G(0.5%), without a statistically significant difference among groups (p > 0.05). The UTS values ranged from 32.85 (±6.08) MPa for G(0.5%) to 35.12 (±5.74) MPa for G(Ctrl) (p > 0.05). MYTAB groups showed antibacterial activity against biofilm formation from 0.5 wt % (p < 0.05) and against planktonic bacteria from 1 wt % (p < 0.05). The higher the MYTAB concentration, the higher the cytotoxic effect, without differences between G(Ctrl) e G(0.5%) (p > 0.05). In conclusion, the addition of 0.5 wt % of MYTAB did not alter the physical and chemical properties of the dental resin and provided antibacterial activity without cytotoxic effect. MDPI 2020-02-15 /pmc/articles/PMC7151596/ /pubmed/32075267 http://dx.doi.org/10.3390/jfb11010009 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mena Silva, Paola Andrea
Garcia, Isadora Martini
Nunes, Julia
Visioli, Fernanda
Castelo Branco Leitune, Vicente
Melo, Mary Anne
Collares, Fabrício Mezzomo
Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study
title Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study
title_full Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study
title_fullStr Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study
title_full_unstemmed Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study
title_short Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study
title_sort myristyltrimethylammonium bromide (mytab) as a cationic surface agent to inhibit streptococcus mutans grown over dental resins: an in vitro study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151596/
https://www.ncbi.nlm.nih.gov/pubmed/32075267
http://dx.doi.org/10.3390/jfb11010009
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