A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1002/jbm.b.35121 http://hdl.handle.net/11449/241257 |
Resumo: | This study aims to evaluate the potential of a novel biomaterial synthesized from amorphous calcium phosphate (ACP), octacalcium phosphate (OCP), and hydroxyapatite (HA) to repair critical-sized defects (CSD) in rabbit calvaria. In vitro analyses of cell viability, cell proliferation, formation of mineral nodules, and cell differentiation using qPCR were performed for comparing experimental calcium phosphate (ECP), deproteinized bovine bone (DBB), and beta-tricalcium phosphate (β-TCP). Bilateral CSDs were created in 45 rabbit calvaria. Six groups were evaluated: ECP, ECP + fibrin sealant (ECP + S), coagulum, autogenous bone, DBB, and β-TCP. Euthanasia was performed at 2, 4, and 8 weeks, followed by micro-computed tomography and histological and immunohistochemical analyses. Results from in vitro analyses revealed similar biocompatibility for all tested materials and a tendency for higher gene expression of some bone markers in the ECP group than in β-TCP and DBB groups at 7 days. In contrast to that in DBB and β-TCP groups, ECP displayed growing bone volume over total volume percentage (BV/TV%) with time in vivo. Histological analysis revealed a greater number of giant cells and reduced size of grafted particles in ECP during all periods of analysis. RUNX-2 expression was statistically lower in ECP than DBB at 2 and 4 weeks. Despite no statistical significance, ECP presented the highest absolute values for ALP-expression at 2, 4, and 8 weeks compared with other groups. Together, our findings indicate that a combination of the ACP, OCP, and HA phases into ECP is beneficial and promising for bone regeneration. |
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A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysisbiomaterialsbone regenerationcalcium phosphatesrabbit calvarial defectThis study aims to evaluate the potential of a novel biomaterial synthesized from amorphous calcium phosphate (ACP), octacalcium phosphate (OCP), and hydroxyapatite (HA) to repair critical-sized defects (CSD) in rabbit calvaria. In vitro analyses of cell viability, cell proliferation, formation of mineral nodules, and cell differentiation using qPCR were performed for comparing experimental calcium phosphate (ECP), deproteinized bovine bone (DBB), and beta-tricalcium phosphate (β-TCP). Bilateral CSDs were created in 45 rabbit calvaria. Six groups were evaluated: ECP, ECP + fibrin sealant (ECP + S), coagulum, autogenous bone, DBB, and β-TCP. Euthanasia was performed at 2, 4, and 8 weeks, followed by micro-computed tomography and histological and immunohistochemical analyses. Results from in vitro analyses revealed similar biocompatibility for all tested materials and a tendency for higher gene expression of some bone markers in the ECP group than in β-TCP and DBB groups at 7 days. In contrast to that in DBB and β-TCP groups, ECP displayed growing bone volume over total volume percentage (BV/TV%) with time in vivo. Histological analysis revealed a greater number of giant cells and reduced size of grafted particles in ECP during all periods of analysis. RUNX-2 expression was statistically lower in ECP than DBB at 2 and 4 weeks. Despite no statistical significance, ECP presented the highest absolute values for ALP-expression at 2, 4, and 8 weeks compared with other groups. Together, our findings indicate that a combination of the ACP, OCP, and HA phases into ECP is beneficial and promising for bone regeneration.Department of Diagnosis and Surgery São Paulo State University (Unesp) School of Dentistry, São PauloDepartment of Oral and Maxillofacial Surgery Massachusetts General Hospital Harvard School of Dental MedicineDepartment of Health Sciences University Center of Araraquara (UNIARA), São PauloDepartment of Physical Chemistry São Paulo State University (Unesp) Institute of Chemistry, São PauloDepartment of Diagnosis and Surgery São Paulo State University (Unesp) School of Dentistry, São PauloDepartment of Physical Chemistry São Paulo State University (Unesp) Institute of Chemistry, São PauloUniversidade Estadual Paulista (UNESP)Harvard School of Dental MedicineUniversity Center of Araraquara (UNIARA)Guastaldi, Fernando Pozzi Semeghini [UNESP]Matheus, Henrique Rinaldi [UNESP]Faloni, Ana Paula de Souzade Almeida-Filho, Edson [UNESP]Cominotte, Mariana Aline [UNESP]Moretti, Livia Alves Correa [UNESP]Verzola, Mario Henrique Arruda [UNESP]Marcantonio, Elcio [UNESP]de Almeida, Juliano Milanezi [UNESP]Guastaldi, Antonio Carlos [UNESP]Cirelli, Joni Augusto [UNESP]2023-03-01T20:53:52Z2023-03-01T20:53:52Z2022-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1002/jbm.b.35121Journal of Biomedical Materials Research - Part B Applied Biomaterials.1552-49811552-4973http://hdl.handle.net/11449/24125710.1002/jbm.b.351212-s2.0-85133168915Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Biomedical Materials Research - Part B Applied Biomaterialsinfo:eu-repo/semantics/openAccess2023-03-01T20:53:53Zoai:repositorio.unesp.br:11449/241257Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:00:45.191781Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis |
title |
A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis |
spellingShingle |
A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis Guastaldi, Fernando Pozzi Semeghini [UNESP] biomaterials bone regeneration calcium phosphates rabbit calvarial defect |
title_short |
A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis |
title_full |
A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis |
title_fullStr |
A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis |
title_full_unstemmed |
A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis |
title_sort |
A new multiphase calcium phosphate graft material improves bone healing—An in vitro and in vivo analysis |
author |
Guastaldi, Fernando Pozzi Semeghini [UNESP] |
author_facet |
Guastaldi, Fernando Pozzi Semeghini [UNESP] Matheus, Henrique Rinaldi [UNESP] Faloni, Ana Paula de Souza de Almeida-Filho, Edson [UNESP] Cominotte, Mariana Aline [UNESP] Moretti, Livia Alves Correa [UNESP] Verzola, Mario Henrique Arruda [UNESP] Marcantonio, Elcio [UNESP] de Almeida, Juliano Milanezi [UNESP] Guastaldi, Antonio Carlos [UNESP] Cirelli, Joni Augusto [UNESP] |
author_role |
author |
author2 |
Matheus, Henrique Rinaldi [UNESP] Faloni, Ana Paula de Souza de Almeida-Filho, Edson [UNESP] Cominotte, Mariana Aline [UNESP] Moretti, Livia Alves Correa [UNESP] Verzola, Mario Henrique Arruda [UNESP] Marcantonio, Elcio [UNESP] de Almeida, Juliano Milanezi [UNESP] Guastaldi, Antonio Carlos [UNESP] Cirelli, Joni Augusto [UNESP] |
author2_role |
author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Harvard School of Dental Medicine University Center of Araraquara (UNIARA) |
dc.contributor.author.fl_str_mv |
Guastaldi, Fernando Pozzi Semeghini [UNESP] Matheus, Henrique Rinaldi [UNESP] Faloni, Ana Paula de Souza de Almeida-Filho, Edson [UNESP] Cominotte, Mariana Aline [UNESP] Moretti, Livia Alves Correa [UNESP] Verzola, Mario Henrique Arruda [UNESP] Marcantonio, Elcio [UNESP] de Almeida, Juliano Milanezi [UNESP] Guastaldi, Antonio Carlos [UNESP] Cirelli, Joni Augusto [UNESP] |
dc.subject.por.fl_str_mv |
biomaterials bone regeneration calcium phosphates rabbit calvarial defect |
topic |
biomaterials bone regeneration calcium phosphates rabbit calvarial defect |
description |
This study aims to evaluate the potential of a novel biomaterial synthesized from amorphous calcium phosphate (ACP), octacalcium phosphate (OCP), and hydroxyapatite (HA) to repair critical-sized defects (CSD) in rabbit calvaria. In vitro analyses of cell viability, cell proliferation, formation of mineral nodules, and cell differentiation using qPCR were performed for comparing experimental calcium phosphate (ECP), deproteinized bovine bone (DBB), and beta-tricalcium phosphate (β-TCP). Bilateral CSDs were created in 45 rabbit calvaria. Six groups were evaluated: ECP, ECP + fibrin sealant (ECP + S), coagulum, autogenous bone, DBB, and β-TCP. Euthanasia was performed at 2, 4, and 8 weeks, followed by micro-computed tomography and histological and immunohistochemical analyses. Results from in vitro analyses revealed similar biocompatibility for all tested materials and a tendency for higher gene expression of some bone markers in the ECP group than in β-TCP and DBB groups at 7 days. In contrast to that in DBB and β-TCP groups, ECP displayed growing bone volume over total volume percentage (BV/TV%) with time in vivo. Histological analysis revealed a greater number of giant cells and reduced size of grafted particles in ECP during all periods of analysis. RUNX-2 expression was statistically lower in ECP than DBB at 2 and 4 weeks. Despite no statistical significance, ECP presented the highest absolute values for ALP-expression at 2, 4, and 8 weeks compared with other groups. Together, our findings indicate that a combination of the ACP, OCP, and HA phases into ECP is beneficial and promising for bone regeneration. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-01-01 2023-03-01T20:53:52Z 2023-03-01T20:53:52Z |
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/10.1002/jbm.b.35121 Journal of Biomedical Materials Research - Part B Applied Biomaterials. 1552-4981 1552-4973 http://hdl.handle.net/11449/241257 10.1002/jbm.b.35121 2-s2.0-85133168915 |
url |
http://dx.doi.org/10.1002/jbm.b.35121 http://hdl.handle.net/11449/241257 |
identifier_str_mv |
Journal of Biomedical Materials Research - Part B Applied Biomaterials. 1552-4981 1552-4973 10.1002/jbm.b.35121 2-s2.0-85133168915 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Biomedical Materials Research - Part B Applied Biomaterials |
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 |
|
_version_ |
1808128593649205248 |