In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1590/1678-7757-2016-0195 http://hdl.handle.net/11449/175384 |
Resumo: | Objectives: Addition of chlorhexidine has enhanced the antimicrobial effect of glass ionomer cement (GIC) indicated to Atraumatic Restorative Treatment (ART); however, the impact of this mixture on the properties of these materials and on the longevity of restorations must be investigated. The aim of this study was to evaluate the effects of incorporating chlorhexidine (CHX) in the in vitro biological and chemical-mechanical properties of GIC and in vivo clinical/ microbiological follow-up of the ART with GIC containing or not CHX. Material and Methods: For in vitro studies, groups were divided into GIC, GIC with 1.25% CHX, and GIC with 2.5% CHX. Antimicrobial activity of GIC was analyzed using agar diffusion and anti-biofilm assays. Cytotoxic effects, compressive tensile strength, microhardness and fluoride (F) release were also evaluated. A randomized controlled trial was conducted on 36 children that received ART either with GIC or GIC with CHX. Saliva and biofilm were collected for mutans streptococci (MS) counts and the survival rate of restorations was checked after 7 days, 3 months and one year after ART. ANOVA/Tukey or Kruskal-Wallis/ Mann-Whitney tests were performed for in vitro tests and in vivo microbiological analysis. The Kaplan-Meier method and Log rank tests were applied to estimate survival percentages of restorations (p<0.05). Results: Incorporation of 1.25% and 2.5% CHX improved the antimicrobial/anti-biofilm activity of GIC, without affecting F release and mechanical characteristics, but 2.5% CHX was cytotoxic. Survival rate of restorations using GIC with 1.25% CHX was similar to GIC. A significant reduction of MS levels was observed for KM+CHX group in children saliva and biofilm 7 days after treatment. Conclusions: The incorporation of 1.25% CHX increased the in vitro antimicrobial activity, without changing chemical-mechanical properties of GIC and odontoblast-like cell viability. This combination improved the in vivo short-term microbiological effect without affecting clinical performance of ART restorations. |
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In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatmentChlorhexidineDental atraumatic restorative treatmentGlass ionomer cementsObjectives: Addition of chlorhexidine has enhanced the antimicrobial effect of glass ionomer cement (GIC) indicated to Atraumatic Restorative Treatment (ART); however, the impact of this mixture on the properties of these materials and on the longevity of restorations must be investigated. The aim of this study was to evaluate the effects of incorporating chlorhexidine (CHX) in the in vitro biological and chemical-mechanical properties of GIC and in vivo clinical/ microbiological follow-up of the ART with GIC containing or not CHX. Material and Methods: For in vitro studies, groups were divided into GIC, GIC with 1.25% CHX, and GIC with 2.5% CHX. Antimicrobial activity of GIC was analyzed using agar diffusion and anti-biofilm assays. Cytotoxic effects, compressive tensile strength, microhardness and fluoride (F) release were also evaluated. A randomized controlled trial was conducted on 36 children that received ART either with GIC or GIC with CHX. Saliva and biofilm were collected for mutans streptococci (MS) counts and the survival rate of restorations was checked after 7 days, 3 months and one year after ART. ANOVA/Tukey or Kruskal-Wallis/ Mann-Whitney tests were performed for in vitro tests and in vivo microbiological analysis. The Kaplan-Meier method and Log rank tests were applied to estimate survival percentages of restorations (p<0.05). Results: Incorporation of 1.25% and 2.5% CHX improved the antimicrobial/anti-biofilm activity of GIC, without affecting F release and mechanical characteristics, but 2.5% CHX was cytotoxic. Survival rate of restorations using GIC with 1.25% CHX was similar to GIC. A significant reduction of MS levels was observed for KM+CHX group in children saliva and biofilm 7 days after treatment. Conclusions: The incorporation of 1.25% CHX increased the in vitro antimicrobial activity, without changing chemical-mechanical properties of GIC and odontoblast-like cell viability. This combination improved the in vivo short-term microbiological effect without affecting clinical performance of ART restorations.Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ)Univ. Estadual Paulista (UNESP) Faculdade de Odontologia de Araçatuba Departamento de Odontologia Infantil e SocialUniversidade Federal Fluminense (UFF) Instituto de Saude de Nova Friburgo Departamento de OdontologiaUniversidade Federal do Rio Grande do Sul (UFRGS) Faculdade de Odontologia Departamento de Odontologia ConservadoraUniversidade Estadual de Campinas (UNICAMP) Faculdade de Odontologia de Piracicaba Departamento de Odontologia InfantilUniv. Estadual Paulista (UNESP) Faculdade de Odontologia de Araraquara Departamento de Fisiologia e PatologiaUniv. Estadual Paulista (UNESP) Faculdade de Odontologia de Araçatuba Departamento de Odontologia Infantil e SocialUniv. Estadual Paulista (UNESP) Faculdade de Odontologia de Araraquara Departamento de Fisiologia e PatologiaFAPERJ: E-26/100.487/2010FAPERJ: E-26/110.205/2011Universidade Estadual Paulista (Unesp)Universidade Federal Fluminense (UFF)Faculdade de OdontologiaUniversidade Estadual de Campinas (UNICAMP)Duque, Cristiane [UNESP]Aida, Kelly Limi [UNESP]Pereira, Jesse Augusto [UNESP]Teixeira, Gláucia SchuindtCaldo-Teixeira, Angela ScarparoPerrone, Luciana RodriguesCaiaffa, Karina Sampaio [UNESP]Negrini, Thais de Cássiade Castilho, Aline Rogéria FreireCosta, Carlos Alberto de Souza [UNESP]2018-12-11T17:15:35Z2018-12-11T17:15:35Z2017-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article541-550application/pdfhttp://dx.doi.org/10.1590/1678-7757-2016-0195Journal of Applied Oral Science, v. 25, n. 5, p. 541-550, 2017.1678-77651678-7757http://hdl.handle.net/11449/17538410.1590/1678-7757-2016-0195S1678-775720170005005412-s2.0-85032212723S1678-77572017000500541.pdf56518745094936170000-0002-2575-279XScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Applied Oral Science0,645info:eu-repo/semantics/openAccess2024-09-27T14:04:28Zoai:repositorio.unesp.br:11449/175384Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:04:28Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment |
title |
In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment |
spellingShingle |
In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment Duque, Cristiane [UNESP] Chlorhexidine Dental atraumatic restorative treatment Glass ionomer cements |
title_short |
In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment |
title_full |
In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment |
title_fullStr |
In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment |
title_full_unstemmed |
In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment |
title_sort |
In vitro and in vivo evaluations of glass-ionomer cement containing chlorhexidine for atraumatic restorative treatment |
author |
Duque, Cristiane [UNESP] |
author_facet |
Duque, Cristiane [UNESP] Aida, Kelly Limi [UNESP] Pereira, Jesse Augusto [UNESP] Teixeira, Gláucia Schuindt Caldo-Teixeira, Angela Scarparo Perrone, Luciana Rodrigues Caiaffa, Karina Sampaio [UNESP] Negrini, Thais de Cássia de Castilho, Aline Rogéria Freire Costa, Carlos Alberto de Souza [UNESP] |
author_role |
author |
author2 |
Aida, Kelly Limi [UNESP] Pereira, Jesse Augusto [UNESP] Teixeira, Gláucia Schuindt Caldo-Teixeira, Angela Scarparo Perrone, Luciana Rodrigues Caiaffa, Karina Sampaio [UNESP] Negrini, Thais de Cássia de Castilho, Aline Rogéria Freire Costa, Carlos Alberto de Souza [UNESP] |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade Federal Fluminense (UFF) Faculdade de Odontologia Universidade Estadual de Campinas (UNICAMP) |
dc.contributor.author.fl_str_mv |
Duque, Cristiane [UNESP] Aida, Kelly Limi [UNESP] Pereira, Jesse Augusto [UNESP] Teixeira, Gláucia Schuindt Caldo-Teixeira, Angela Scarparo Perrone, Luciana Rodrigues Caiaffa, Karina Sampaio [UNESP] Negrini, Thais de Cássia de Castilho, Aline Rogéria Freire Costa, Carlos Alberto de Souza [UNESP] |
dc.subject.por.fl_str_mv |
Chlorhexidine Dental atraumatic restorative treatment Glass ionomer cements |
topic |
Chlorhexidine Dental atraumatic restorative treatment Glass ionomer cements |
description |
Objectives: Addition of chlorhexidine has enhanced the antimicrobial effect of glass ionomer cement (GIC) indicated to Atraumatic Restorative Treatment (ART); however, the impact of this mixture on the properties of these materials and on the longevity of restorations must be investigated. The aim of this study was to evaluate the effects of incorporating chlorhexidine (CHX) in the in vitro biological and chemical-mechanical properties of GIC and in vivo clinical/ microbiological follow-up of the ART with GIC containing or not CHX. Material and Methods: For in vitro studies, groups were divided into GIC, GIC with 1.25% CHX, and GIC with 2.5% CHX. Antimicrobial activity of GIC was analyzed using agar diffusion and anti-biofilm assays. Cytotoxic effects, compressive tensile strength, microhardness and fluoride (F) release were also evaluated. A randomized controlled trial was conducted on 36 children that received ART either with GIC or GIC with CHX. Saliva and biofilm were collected for mutans streptococci (MS) counts and the survival rate of restorations was checked after 7 days, 3 months and one year after ART. ANOVA/Tukey or Kruskal-Wallis/ Mann-Whitney tests were performed for in vitro tests and in vivo microbiological analysis. The Kaplan-Meier method and Log rank tests were applied to estimate survival percentages of restorations (p<0.05). Results: Incorporation of 1.25% and 2.5% CHX improved the antimicrobial/anti-biofilm activity of GIC, without affecting F release and mechanical characteristics, but 2.5% CHX was cytotoxic. Survival rate of restorations using GIC with 1.25% CHX was similar to GIC. A significant reduction of MS levels was observed for KM+CHX group in children saliva and biofilm 7 days after treatment. Conclusions: The incorporation of 1.25% CHX increased the in vitro antimicrobial activity, without changing chemical-mechanical properties of GIC and odontoblast-like cell viability. This combination improved the in vivo short-term microbiological effect without affecting clinical performance of ART restorations. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-09-01 2018-12-11T17:15:35Z 2018-12-11T17:15:35Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/1678-7757-2016-0195 Journal of Applied Oral Science, v. 25, n. 5, p. 541-550, 2017. 1678-7765 1678-7757 http://hdl.handle.net/11449/175384 10.1590/1678-7757-2016-0195 S1678-77572017000500541 2-s2.0-85032212723 S1678-77572017000500541.pdf 5651874509493617 0000-0002-2575-279X |
url |
http://dx.doi.org/10.1590/1678-7757-2016-0195 http://hdl.handle.net/11449/175384 |
identifier_str_mv |
Journal of Applied Oral Science, v. 25, n. 5, p. 541-550, 2017. 1678-7765 1678-7757 10.1590/1678-7757-2016-0195 S1678-77572017000500541 2-s2.0-85032212723 S1678-77572017000500541.pdf 5651874509493617 0000-0002-2575-279X |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Applied Oral Science 0,645 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
541-550 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1813546386347524096 |