Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1007/s10856-021-06604-9 http://hdl.handle.net/11449/229943 |
Resumo: | This study aimed to investigate the antimicrobial and biological properties of Ambroxol associated with glycerin (GLI), propylene glycol (PG), and polyethylene glycol (PEG) as a possible vehicle for an experimental tricalcium silicate sealer, with the intention of developing a new biomaterial. Mouse undifferentiated dental pulp cells (OD-21) were cultured, and the effects of different association on cell proliferation and inflammatory cytokine production were investigated. Antimicrobial adhesion of Enterococcus faecalis to setting sealers at 2 h was evaluated. Polyethylene tubes containing experimental sealers and empty tubes were implanted into dorsal connective tissues of 12 male 3- to 4-months-old Wistar rats (250–280 g). After 7 and 30 days, the tubes were removed and processed for histological and immunohistochemical analyses. ANOVA followed by Bonferroni correction and ANOVA followed by Tukey test was used for parametric data and Kruskal–Wallis followed by Dunn for nonparametric (p < 0.05). Cell proliferation was dose-dependent, since all association were cytotoxic at higher concentrations; however, Ambroxol–PEG showed significantly higher cytotoxicity than other association (p < 0.05). In addition, irrespective of the association, no cytokine production was observed in vitro. Ambroxol–GLI reduced bacterial viability, whereas Ambroxol–PEG increased (p < 0.05). Histological examination showed no significant difference in the inflammatory response (p > 0.05) and mineralization ability in all association. Additionally, IL-1β and TNF-α were upregulated on Ambroxol–PEG in relation to Control at 07 days (p < 0.05). Ambroxol–GLI was the best vehicle for experimental tricalcium silicate sealer, as it promoted an increase in antimicrobial activity without altering the inflammatory response or mineralization ability. [Figure not available: see fulltext.] |
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Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealerThis study aimed to investigate the antimicrobial and biological properties of Ambroxol associated with glycerin (GLI), propylene glycol (PG), and polyethylene glycol (PEG) as a possible vehicle for an experimental tricalcium silicate sealer, with the intention of developing a new biomaterial. Mouse undifferentiated dental pulp cells (OD-21) were cultured, and the effects of different association on cell proliferation and inflammatory cytokine production were investigated. Antimicrobial adhesion of Enterococcus faecalis to setting sealers at 2 h was evaluated. Polyethylene tubes containing experimental sealers and empty tubes were implanted into dorsal connective tissues of 12 male 3- to 4-months-old Wistar rats (250–280 g). After 7 and 30 days, the tubes were removed and processed for histological and immunohistochemical analyses. ANOVA followed by Bonferroni correction and ANOVA followed by Tukey test was used for parametric data and Kruskal–Wallis followed by Dunn for nonparametric (p < 0.05). Cell proliferation was dose-dependent, since all association were cytotoxic at higher concentrations; however, Ambroxol–PEG showed significantly higher cytotoxicity than other association (p < 0.05). In addition, irrespective of the association, no cytokine production was observed in vitro. Ambroxol–GLI reduced bacterial viability, whereas Ambroxol–PEG increased (p < 0.05). Histological examination showed no significant difference in the inflammatory response (p > 0.05) and mineralization ability in all association. Additionally, IL-1β and TNF-α were upregulated on Ambroxol–PEG in relation to Control at 07 days (p < 0.05). Ambroxol–GLI was the best vehicle for experimental tricalcium silicate sealer, as it promoted an increase in antimicrobial activity without altering the inflammatory response or mineralization ability. [Figure not available: see fulltext.]Department of Dentistry Endodontics and Dental Materials University of São Paulo (USP) Bauru School of Dentistry, Alameda Octávio Pinheiro BrisollaDepartment of Oral and Maxillofacial Surgery and Integrated Clinic School of Dentistry Araçatuba São Paulo State University (Unesp)Department of Endodontics School of Dentistry Araçatuba São Paulo State University (Unesp), Rua José BonifácioDepartment of Basic Science School of Dentistry Araçatuba São Paulo State University (Unesp), Rua José BonifácioDepartment of Dentistry School of Dentistry of Sobral Federal University of Ceará (UFC), Rua Coronel Estanislau FrotaDepartment of Oral and Maxillofacial Surgery and Integrated Clinic School of Dentistry Araçatuba São Paulo State University (Unesp)Department of Endodontics School of Dentistry Araçatuba São Paulo State University (Unesp), Rua José BonifácioDepartment of Basic Science School of Dentistry Araçatuba São Paulo State University (Unesp), Rua José BonifácioUniversidade de São Paulo (USP)Universidade Estadual Paulista (UNESP)Federal University of Ceará (UFC)de Azevedo Queiroz, Índia OlintaMachado, Thiago [UNESP]Alves, Camila Carneiro [UNESP]Brito, Victor Gustavo Balera [UNESP]de Vasconcelos, Bruno CarvalhoGomes-Filho, João Eduardo [UNESP]Ervolino, Edilson [UNESP]de Oliveira, Sandra Helena Penha [UNESP]Duarte, Marco Antonio Hungaro2022-04-29T08:36:45Z2022-04-29T08:36:45Z2021-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s10856-021-06604-9Journal of Materials Science: Materials in Medicine, v. 32, n. 12, 2021.1573-48380957-4530http://hdl.handle.net/11449/22994310.1007/s10856-021-06604-92-s2.0-85119855082Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Materials Science: Materials in Medicineinfo:eu-repo/semantics/openAccess2024-09-19T18:31:42Zoai:repositorio.unesp.br:11449/229943Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-19T18:31:42Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer |
title |
Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer |
spellingShingle |
Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer de Azevedo Queiroz, Índia Olinta |
title_short |
Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer |
title_full |
Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer |
title_fullStr |
Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer |
title_full_unstemmed |
Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer |
title_sort |
Biological and antimicrobial properties of the association Ambroxol and a water-soluble viscous liquid as a vehicle for a tricalcium silicate-based sealer |
author |
de Azevedo Queiroz, Índia Olinta |
author_facet |
de Azevedo Queiroz, Índia Olinta Machado, Thiago [UNESP] Alves, Camila Carneiro [UNESP] Brito, Victor Gustavo Balera [UNESP] de Vasconcelos, Bruno Carvalho Gomes-Filho, João Eduardo [UNESP] Ervolino, Edilson [UNESP] de Oliveira, Sandra Helena Penha [UNESP] Duarte, Marco Antonio Hungaro |
author_role |
author |
author2 |
Machado, Thiago [UNESP] Alves, Camila Carneiro [UNESP] Brito, Victor Gustavo Balera [UNESP] de Vasconcelos, Bruno Carvalho Gomes-Filho, João Eduardo [UNESP] Ervolino, Edilson [UNESP] de Oliveira, Sandra Helena Penha [UNESP] Duarte, Marco Antonio Hungaro |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual Paulista (UNESP) Federal University of Ceará (UFC) |
dc.contributor.author.fl_str_mv |
de Azevedo Queiroz, Índia Olinta Machado, Thiago [UNESP] Alves, Camila Carneiro [UNESP] Brito, Victor Gustavo Balera [UNESP] de Vasconcelos, Bruno Carvalho Gomes-Filho, João Eduardo [UNESP] Ervolino, Edilson [UNESP] de Oliveira, Sandra Helena Penha [UNESP] Duarte, Marco Antonio Hungaro |
description |
This study aimed to investigate the antimicrobial and biological properties of Ambroxol associated with glycerin (GLI), propylene glycol (PG), and polyethylene glycol (PEG) as a possible vehicle for an experimental tricalcium silicate sealer, with the intention of developing a new biomaterial. Mouse undifferentiated dental pulp cells (OD-21) were cultured, and the effects of different association on cell proliferation and inflammatory cytokine production were investigated. Antimicrobial adhesion of Enterococcus faecalis to setting sealers at 2 h was evaluated. Polyethylene tubes containing experimental sealers and empty tubes were implanted into dorsal connective tissues of 12 male 3- to 4-months-old Wistar rats (250–280 g). After 7 and 30 days, the tubes were removed and processed for histological and immunohistochemical analyses. ANOVA followed by Bonferroni correction and ANOVA followed by Tukey test was used for parametric data and Kruskal–Wallis followed by Dunn for nonparametric (p < 0.05). Cell proliferation was dose-dependent, since all association were cytotoxic at higher concentrations; however, Ambroxol–PEG showed significantly higher cytotoxicity than other association (p < 0.05). In addition, irrespective of the association, no cytokine production was observed in vitro. Ambroxol–GLI reduced bacterial viability, whereas Ambroxol–PEG increased (p < 0.05). Histological examination showed no significant difference in the inflammatory response (p > 0.05) and mineralization ability in all association. Additionally, IL-1β and TNF-α were upregulated on Ambroxol–PEG in relation to Control at 07 days (p < 0.05). Ambroxol–GLI was the best vehicle for experimental tricalcium silicate sealer, as it promoted an increase in antimicrobial activity without altering the inflammatory response or mineralization ability. [Figure not available: see fulltext.] |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-12-01 2022-04-29T08:36:45Z 2022-04-29T08:36:45Z |
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/10.1007/s10856-021-06604-9 Journal of Materials Science: Materials in Medicine, v. 32, n. 12, 2021. 1573-4838 0957-4530 http://hdl.handle.net/11449/229943 10.1007/s10856-021-06604-9 2-s2.0-85119855082 |
url |
http://dx.doi.org/10.1007/s10856-021-06604-9 http://hdl.handle.net/11449/229943 |
identifier_str_mv |
Journal of Materials Science: Materials in Medicine, v. 32, n. 12, 2021. 1573-4838 0957-4530 10.1007/s10856-021-06604-9 2-s2.0-85119855082 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Materials Science: Materials in Medicine |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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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1813546445840580608 |