Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria
Main Author: | |
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Publication Date: | 2018 |
Other Authors: | , , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.1590/1678-7757-2016-0531 http://hdl.handle.net/11449/175776 |
Summary: | Objective: The aim of this study was to evaluate the osteoconductive potential of BoneCeramic™ on bone healing in rat calvaria 5-mm defects. Material and Methods: A 5-mm calvaria bone defect was induced in three groups and the defect was not filled with biomaterial [Clot Group (CG)], autogenous bone (AG), or Bone Ceramic Group (BCG). Animals were euthanized after 14 or 28 days and the bone tissue within the central area of the bone defect was evaluated. Results were compared using ANOVA and Tukey test (p<0.05). Immunohistochemistry was performed using primary antibodies against osteocalcin, RUNX-2, TRAP, VEGF proteins, and 3-dimensional images of the defects in µCT were obtained to calculate bone mineral density (BMD). Results: In BCG, the defect was completely filled with biomaterial and new bone formation, which was statistically superior to that in the GC group, at both time-points (p<0.001 for 14 days; p=0.002 for 28 days). TRAP protein showed weak, RUNX-2 showed a greater immunolabeling when compared with other groups, VEGF showed moderate immunostaining, while osteocalcin was present at all time-points analyzed. The µCT images showed filling defect by BCG (BMD= 1337 HU at 28 days). Conclusion: Therefore, the biomaterial tested was found to be favorable to fill bone defects for the reporting period analyzed. |
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Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvariaBiocompatible materialsBone regenerationImmunohistochemistryObjective: The aim of this study was to evaluate the osteoconductive potential of BoneCeramic™ on bone healing in rat calvaria 5-mm defects. Material and Methods: A 5-mm calvaria bone defect was induced in three groups and the defect was not filled with biomaterial [Clot Group (CG)], autogenous bone (AG), or Bone Ceramic Group (BCG). Animals were euthanized after 14 or 28 days and the bone tissue within the central area of the bone defect was evaluated. Results were compared using ANOVA and Tukey test (p<0.05). Immunohistochemistry was performed using primary antibodies against osteocalcin, RUNX-2, TRAP, VEGF proteins, and 3-dimensional images of the defects in µCT were obtained to calculate bone mineral density (BMD). Results: In BCG, the defect was completely filled with biomaterial and new bone formation, which was statistically superior to that in the GC group, at both time-points (p<0.001 for 14 days; p=0.002 for 28 days). TRAP protein showed weak, RUNX-2 showed a greater immunolabeling when compared with other groups, VEGF showed moderate immunostaining, while osteocalcin was present at all time-points analyzed. The µCT images showed filling defect by BCG (BMD= 1337 HU at 28 days). Conclusion: Therefore, the biomaterial tested was found to be favorable to fill bone defects for the reporting period analyzed.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Univ. Estadual Paulista (UNESP) Faculdade de Odontologia de Araçatuba Departamento de Cirurgia e Clínica IntegradaUniversidade do Sagrado Coração Departamento de Ciências da SaúdeUniv. Estadual Paulista (UNESP) Faculdade de Odontologia de Araçatuba Departamento de Ciências BásicasUniv. Estadual Paulista (UNESP) Faculdade de Odontologia de Araçatuba Departamento de Cirurgia e Clínica IntegradaUniv. Estadual Paulista (UNESP) Faculdade de Odontologia de Araçatuba Departamento de Ciências BásicasFAPESP: #2012/06309-0Universidade Estadual Paulista (Unesp)Universidade do Sagrado CoraçãoFabris, André Luis da Silva [UNESP]Faverani, Leonardo Perez [UNESP]Gomes-Ferreira, Pedro Henrique Silva [UNESP]Polo, Tárik Ocon Braga [UNESP]Santiago-Júnior, Joel FerreiraOkamoto, Roberta [UNESP]2018-12-11T17:17:27Z2018-12-11T17:17:27Z2018-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1590/1678-7757-2016-0531Journal of Applied Oral Science, v. 26.1678-77651678-7757http://hdl.handle.net/11449/17577610.1590/1678-7757-2016-0531S1678-775720180001004012-s2.0-85040979077S1678-77572018000100401.pdf1527011976590326Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Applied Oral Science0,645info:eu-repo/semantics/openAccess2024-09-19T14:02:45Zoai:repositorio.unesp.br:11449/175776Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-19T14:02:45Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria |
title |
Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria |
spellingShingle |
Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria Fabris, André Luis da Silva [UNESP] Biocompatible materials Bone regeneration Immunohistochemistry |
title_short |
Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria |
title_full |
Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria |
title_fullStr |
Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria |
title_full_unstemmed |
Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria |
title_sort |
Bone repair access of boneceramic™ in 5-mm defects: Study on rat calvaria |
author |
Fabris, André Luis da Silva [UNESP] |
author_facet |
Fabris, André Luis da Silva [UNESP] Faverani, Leonardo Perez [UNESP] Gomes-Ferreira, Pedro Henrique Silva [UNESP] Polo, Tárik Ocon Braga [UNESP] Santiago-Júnior, Joel Ferreira Okamoto, Roberta [UNESP] |
author_role |
author |
author2 |
Faverani, Leonardo Perez [UNESP] Gomes-Ferreira, Pedro Henrique Silva [UNESP] Polo, Tárik Ocon Braga [UNESP] Santiago-Júnior, Joel Ferreira Okamoto, Roberta [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade do Sagrado Coração |
dc.contributor.author.fl_str_mv |
Fabris, André Luis da Silva [UNESP] Faverani, Leonardo Perez [UNESP] Gomes-Ferreira, Pedro Henrique Silva [UNESP] Polo, Tárik Ocon Braga [UNESP] Santiago-Júnior, Joel Ferreira Okamoto, Roberta [UNESP] |
dc.subject.por.fl_str_mv |
Biocompatible materials Bone regeneration Immunohistochemistry |
topic |
Biocompatible materials Bone regeneration Immunohistochemistry |
description |
Objective: The aim of this study was to evaluate the osteoconductive potential of BoneCeramic™ on bone healing in rat calvaria 5-mm defects. Material and Methods: A 5-mm calvaria bone defect was induced in three groups and the defect was not filled with biomaterial [Clot Group (CG)], autogenous bone (AG), or Bone Ceramic Group (BCG). Animals were euthanized after 14 or 28 days and the bone tissue within the central area of the bone defect was evaluated. Results were compared using ANOVA and Tukey test (p<0.05). Immunohistochemistry was performed using primary antibodies against osteocalcin, RUNX-2, TRAP, VEGF proteins, and 3-dimensional images of the defects in µCT were obtained to calculate bone mineral density (BMD). Results: In BCG, the defect was completely filled with biomaterial and new bone formation, which was statistically superior to that in the GC group, at both time-points (p<0.001 for 14 days; p=0.002 for 28 days). TRAP protein showed weak, RUNX-2 showed a greater immunolabeling when compared with other groups, VEGF showed moderate immunostaining, while osteocalcin was present at all time-points analyzed. The µCT images showed filling defect by BCG (BMD= 1337 HU at 28 days). Conclusion: Therefore, the biomaterial tested was found to be favorable to fill bone defects for the reporting period analyzed. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:17:27Z 2018-12-11T17:17:27Z 2018-01-01 |
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/10.1590/1678-7757-2016-0531 Journal of Applied Oral Science, v. 26. 1678-7765 1678-7757 http://hdl.handle.net/11449/175776 10.1590/1678-7757-2016-0531 S1678-77572018000100401 2-s2.0-85040979077 S1678-77572018000100401.pdf 1527011976590326 |
url |
http://dx.doi.org/10.1590/1678-7757-2016-0531 http://hdl.handle.net/11449/175776 |
identifier_str_mv |
Journal of Applied Oral Science, v. 26. 1678-7765 1678-7757 10.1590/1678-7757-2016-0531 S1678-77572018000100401 2-s2.0-85040979077 S1678-77572018000100401.pdf 1527011976590326 |
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 |
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) |
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UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
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Repositório Institucional da UNESP |
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Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1834483234173353984 |