Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials

Detalhes bibliográficos
Autor(a) principal: Benetti, Francine [UNESP]
Data de Publicação: 2020
Outros Autores: Bueno, Carlos Roberto Emerenciano [UNESP], Dos Reis-Prado, Alexandre Henrique, Souza, Marina Trevelin, Goto, Juliana [UNESP], de Camargo, Jose Maurício Paradella [UNESP], Duarte, Marco Antônio Húngaro, Dezan-Júnior, Elói [UNESP], Zanotto, Edgar Dutra, Cintra, Luciano Tavares Angelo [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/0103-6440202003660
http://hdl.handle.net/11449/208108
Resumo: This study evaluated the biocompatibility, biomineralization, and collagen fiber maturation induced by Resorbable Tissue Replacement (RTR®; β-tricalcium phosphate [TCP]), Bioglass (BIOG; bioactive glass), and DM Bone® (DMB; hydroxyapatite and β-TCP) in vivo. Sixty-four polyethylene tubes with or without (control group; CG) materials (n=8/group/period) were randomly implanted in the subcutaneous tissue of 16 male Wistar rats (four per rat), weighting 250 to 280 g. The rats were killed after 7 and 30 days (n=8), and the specimens were removed for analysis of inflammation using hematoxylin-eosin; biomineralization assay using von Kossa (VK) staining and polarized light (PL); and collagen fiber maturation using picrosirius red (PSR). Nonparametric data were statistically analyzed by Kruskal-Wallis and Dunn tests, and parametric data by one-way ANOVA test (p<0.05). At 7 days, all groups induced moderate inflammation (p>0.05). At 30 days, there was mild inflammation in the BIOG and CG, and moderate inflammation in the RTR and DMB groups, with a significant difference between the CG and RTR (p<0.05). The fibrous capsule was thick at 7 days and predominantly thin at 30 days in all groups. All materials exhibited structures that stained positively for VK and PL. Immature collagen fibers were predominant at 7 and 30 days in all groups (p>0.05), although DMB exhibited more mature fibers than BIOG at 30 days (p<0.05). RTR, BIOG, and DMB were biocompatible, inducing inflammation that reduced over time and biomineralization in the subcutaneous tissue of rats. DMB exhibited more mature collagen fibers than BIOG over a longer period.
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spelling Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materialsBiocompatibilityBioglassBiomineralizationBone regenerationβ-tricalcium phosphateThis study evaluated the biocompatibility, biomineralization, and collagen fiber maturation induced by Resorbable Tissue Replacement (RTR®; β-tricalcium phosphate [TCP]), Bioglass (BIOG; bioactive glass), and DM Bone® (DMB; hydroxyapatite and β-TCP) in vivo. Sixty-four polyethylene tubes with or without (control group; CG) materials (n=8/group/period) were randomly implanted in the subcutaneous tissue of 16 male Wistar rats (four per rat), weighting 250 to 280 g. The rats were killed after 7 and 30 days (n=8), and the specimens were removed for analysis of inflammation using hematoxylin-eosin; biomineralization assay using von Kossa (VK) staining and polarized light (PL); and collagen fiber maturation using picrosirius red (PSR). Nonparametric data were statistically analyzed by Kruskal-Wallis and Dunn tests, and parametric data by one-way ANOVA test (p<0.05). At 7 days, all groups induced moderate inflammation (p>0.05). At 30 days, there was mild inflammation in the BIOG and CG, and moderate inflammation in the RTR and DMB groups, with a significant difference between the CG and RTR (p<0.05). The fibrous capsule was thick at 7 days and predominantly thin at 30 days in all groups. All materials exhibited structures that stained positively for VK and PL. Immature collagen fibers were predominant at 7 and 30 days in all groups (p>0.05), although DMB exhibited more mature fibers than BIOG at 30 days (p<0.05). RTR, BIOG, and DMB were biocompatible, inducing inflammation that reduced over time and biomineralization in the subcutaneous tissue of rats. DMB exhibited more mature collagen fibers than BIOG over a longer period.Universidade Federal de Minas GeraisDepartment of Restorative Dentistry School of Dentistry UFMG-Universidade Federal de Minas GeraisDepartment of Endodontics School of Dentistry UNESP-Universidade Estadual PaulistaDepartment of Materials Engineering Vitreous Materials Laboratory (LaMaV) UFSCar-Universidade Federal de São CarlosDepartment of Dentistry Endodontics and Dental Materials School of Dentistry USP – Universidade de São PauloDepartment of Endodontics School of Dentistry UNESP-Universidade Estadual PaulistaUniversidade Federal de Minas Gerais (UFMG)Universidade Estadual Paulista (Unesp)Universidade Federal de São Carlos (UFSCar)Universidade de São Paulo (USP)Benetti, Francine [UNESP]Bueno, Carlos Roberto Emerenciano [UNESP]Dos Reis-Prado, Alexandre HenriqueSouza, Marina TrevelinGoto, Juliana [UNESP]de Camargo, Jose Maurício Paradella [UNESP]Duarte, Marco Antônio HúngaroDezan-Júnior, Elói [UNESP]Zanotto, Edgar DutraCintra, Luciano Tavares Angelo [UNESP]2021-06-25T11:06:30Z2021-06-25T11:06:30Z2020-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article477-484application/pdfhttp://dx.doi.org/10.1590/0103-6440202003660Brazilian Dental Journal, v. 31, n. 5, p. 477-484, 2020.1806-47600103-6440http://hdl.handle.net/11449/20810810.1590/0103-6440202003660S0103-644020200005004772-s2.0-85095123663S0103-64402020000500477.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBrazilian Dental Journalinfo:eu-repo/semantics/openAccess2024-01-19T06:32:58Zoai:repositorio.unesp.br:11449/208108Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-19T06:32:58Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials
title Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials
spellingShingle Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials
Benetti, Francine [UNESP]
Biocompatibility
Bioglass
Biomineralization
Bone regeneration
β-tricalcium phosphate
title_short Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials
title_full Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials
title_fullStr Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials
title_full_unstemmed Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials
title_sort Biocompatibility, biomineralization, and maturation of collagen by rtr®, bioglass and dm bone® materials
author Benetti, Francine [UNESP]
author_facet Benetti, Francine [UNESP]
Bueno, Carlos Roberto Emerenciano [UNESP]
Dos Reis-Prado, Alexandre Henrique
Souza, Marina Trevelin
Goto, Juliana [UNESP]
de Camargo, Jose Maurício Paradella [UNESP]
Duarte, Marco Antônio Húngaro
Dezan-Júnior, Elói [UNESP]
Zanotto, Edgar Dutra
Cintra, Luciano Tavares Angelo [UNESP]
author_role author
author2 Bueno, Carlos Roberto Emerenciano [UNESP]
Dos Reis-Prado, Alexandre Henrique
Souza, Marina Trevelin
Goto, Juliana [UNESP]
de Camargo, Jose Maurício Paradella [UNESP]
Duarte, Marco Antônio Húngaro
Dezan-Júnior, Elói [UNESP]
Zanotto, Edgar Dutra
Cintra, Luciano Tavares Angelo [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Minas Gerais (UFMG)
Universidade Estadual Paulista (Unesp)
Universidade Federal de São Carlos (UFSCar)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Benetti, Francine [UNESP]
Bueno, Carlos Roberto Emerenciano [UNESP]
Dos Reis-Prado, Alexandre Henrique
Souza, Marina Trevelin
Goto, Juliana [UNESP]
de Camargo, Jose Maurício Paradella [UNESP]
Duarte, Marco Antônio Húngaro
Dezan-Júnior, Elói [UNESP]
Zanotto, Edgar Dutra
Cintra, Luciano Tavares Angelo [UNESP]
dc.subject.por.fl_str_mv Biocompatibility
Bioglass
Biomineralization
Bone regeneration
β-tricalcium phosphate
topic Biocompatibility
Bioglass
Biomineralization
Bone regeneration
β-tricalcium phosphate
description This study evaluated the biocompatibility, biomineralization, and collagen fiber maturation induced by Resorbable Tissue Replacement (RTR®; β-tricalcium phosphate [TCP]), Bioglass (BIOG; bioactive glass), and DM Bone® (DMB; hydroxyapatite and β-TCP) in vivo. Sixty-four polyethylene tubes with or without (control group; CG) materials (n=8/group/period) were randomly implanted in the subcutaneous tissue of 16 male Wistar rats (four per rat), weighting 250 to 280 g. The rats were killed after 7 and 30 days (n=8), and the specimens were removed for analysis of inflammation using hematoxylin-eosin; biomineralization assay using von Kossa (VK) staining and polarized light (PL); and collagen fiber maturation using picrosirius red (PSR). Nonparametric data were statistically analyzed by Kruskal-Wallis and Dunn tests, and parametric data by one-way ANOVA test (p<0.05). At 7 days, all groups induced moderate inflammation (p>0.05). At 30 days, there was mild inflammation in the BIOG and CG, and moderate inflammation in the RTR and DMB groups, with a significant difference between the CG and RTR (p<0.05). The fibrous capsule was thick at 7 days and predominantly thin at 30 days in all groups. All materials exhibited structures that stained positively for VK and PL. Immature collagen fibers were predominant at 7 and 30 days in all groups (p>0.05), although DMB exhibited more mature fibers than BIOG at 30 days (p<0.05). RTR, BIOG, and DMB were biocompatible, inducing inflammation that reduced over time and biomineralization in the subcutaneous tissue of rats. DMB exhibited more mature collagen fibers than BIOG over a longer period.
publishDate 2020
dc.date.none.fl_str_mv 2020-09-01
2021-06-25T11:06:30Z
2021-06-25T11:06:30Z
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/10.1590/0103-6440202003660
Brazilian Dental Journal, v. 31, n. 5, p. 477-484, 2020.
1806-4760
0103-6440
http://hdl.handle.net/11449/208108
10.1590/0103-6440202003660
S0103-64402020000500477
2-s2.0-85095123663
S0103-64402020000500477.pdf
url http://dx.doi.org/10.1590/0103-6440202003660
http://hdl.handle.net/11449/208108
identifier_str_mv Brazilian Dental Journal, v. 31, n. 5, p. 477-484, 2020.
1806-4760
0103-6440
10.1590/0103-6440202003660
S0103-64402020000500477
2-s2.0-85095123663
S0103-64402020000500477.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brazilian Dental Journal
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 477-484
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
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