Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects

Bibliographic Details
Main Author: Muñoz, Eladio
Publication Date: 2024
Other Authors: Loyola, Ana Carolina, Pitol-Palin, Leticia [UNESP], Okamoto, Roberta [UNESP], Shibli, Jamil, Messora, Michel, Novaes, Arthur Belém, Scombatti de Souza, Sergio
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1089/ten.tec.2024.0214
https://hdl.handle.net/11449/304126
Summary: This study evaluated the efficacy of synthetic bone blocks, composed of hydroxyapatite (HA) or β-tricalcium phosphate (B-TCP), which were produced by additive manufacturing and used for the repair of critical size bone defects (CSDs) in rat calvaria. Sixty rats were divided into five groups (n = 12): blood clot (CONTROL), 3D-printed HA (HA), 3D-printed β-TCP (B-TCP), 3D-printed HA + autologous micrograft (HA+RIG), and 3D-printed β-TCP + autologous micrograft (B-TCP+RIG). CSDs were surgically created in the parietal bone and treated with the respective biomaterials. The animals were euthanized at 30 and 60 days postsurgery for microcomputed tomography (micro-CT) histomorphometric, and immunohistochemical analysis to assess new bone formation. Micro-CT analysis showed that both biomaterials were incorporated into the animals’ calvaria. The HA+RIG group, especially at 60 days, exhibited a significant increase in bone formation compared with the control. The use of 3D-printed bioceramics resulted in thinner trabeculae but a higher number of trabeculae compared with the control. Histomorphometric analysis showed bone islands in close contact with the B-TCP and HA blocks at 30 days. The HA blocks (HA and HA+RIG groups) showed statistically higher new bone formation values with further improvement when autologous micrografts were included. Immunohistochemical analysis showed the expression of bone repair proteins. At 30 days, the HA+RIG group had moderate Osteopontin (OPN) staining, indicating that the repair process had started, whereas other groups showed no staining. At 60 days, the HA+RIG group showed slight staining, similar to that of the control. Osteocalcin (OCN) staining, indicating osteoblastic activity, showed moderate expression in the HA and HA+RIG groups at 30 days, with slight expression in the B-TCP and B-TCP+RIG groups. The combination of HA blocks with autologous micrografts significantly enhanced bone repair, suggesting that the presence of progenitor cells and growth factors in the micrografts contributed to the improved outcomes. It was concluded that 3D-printed bone substitute blocks, associated with autologous micrografts, are highly effective in promoting bone repair in CSDs in rat calvaria.
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spelling Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects3D-printed scaffoldsadditive manufacturebone regenerationhydroxyapatiteβ-tricalcium phosphateThis study evaluated the efficacy of synthetic bone blocks, composed of hydroxyapatite (HA) or β-tricalcium phosphate (B-TCP), which were produced by additive manufacturing and used for the repair of critical size bone defects (CSDs) in rat calvaria. Sixty rats were divided into five groups (n = 12): blood clot (CONTROL), 3D-printed HA (HA), 3D-printed β-TCP (B-TCP), 3D-printed HA + autologous micrograft (HA+RIG), and 3D-printed β-TCP + autologous micrograft (B-TCP+RIG). CSDs were surgically created in the parietal bone and treated with the respective biomaterials. The animals were euthanized at 30 and 60 days postsurgery for microcomputed tomography (micro-CT) histomorphometric, and immunohistochemical analysis to assess new bone formation. Micro-CT analysis showed that both biomaterials were incorporated into the animals’ calvaria. The HA+RIG group, especially at 60 days, exhibited a significant increase in bone formation compared with the control. The use of 3D-printed bioceramics resulted in thinner trabeculae but a higher number of trabeculae compared with the control. Histomorphometric analysis showed bone islands in close contact with the B-TCP and HA blocks at 30 days. The HA blocks (HA and HA+RIG groups) showed statistically higher new bone formation values with further improvement when autologous micrografts were included. Immunohistochemical analysis showed the expression of bone repair proteins. At 30 days, the HA+RIG group had moderate Osteopontin (OPN) staining, indicating that the repair process had started, whereas other groups showed no staining. At 60 days, the HA+RIG group showed slight staining, similar to that of the control. Osteocalcin (OCN) staining, indicating osteoblastic activity, showed moderate expression in the HA and HA+RIG groups at 30 days, with slight expression in the B-TCP and B-TCP+RIG groups. The combination of HA blocks with autologous micrografts significantly enhanced bone repair, suggesting that the presence of progenitor cells and growth factors in the micrografts contributed to the improved outcomes. It was concluded that 3D-printed bone substitute blocks, associated with autologous micrografts, are highly effective in promoting bone repair in CSDs in rat calvaria.School of Dentistry of Ribeirao Preto University of Sao PauloAraçatuba Dental School São Paulo State University UNESPPlenum Bioengenharia M3 Health Indústria e Comércio de Produtos Médicos Odontológicos e Correlatos S.ADepartment of Periodontology Dental Research Division Guarulhos UniversityAraçatuba Dental School São Paulo State University UNESPUniversidade de São Paulo (USP)Universidade Estadual Paulista (UNESP)Odontológicos e Correlatos S.AGuarulhos UniversityMuñoz, EladioLoyola, Ana CarolinaPitol-Palin, Leticia [UNESP]Okamoto, Roberta [UNESP]Shibli, JamilMessora, MichelNovaes, Arthur BelémScombatti de Souza, Sergio2025-04-29T19:33:55Z2024-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article533-546http://dx.doi.org/10.1089/ten.tec.2024.0214Tissue Engineering - Part C: Methods, v. 30, n. 11, p. 533-546, 2024.1937-33921937-3384https://hdl.handle.net/11449/30412610.1089/ten.tec.2024.02142-s2.0-85207119728Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengTissue Engineering - Part C: Methodsinfo:eu-repo/semantics/openAccess2025-05-01T05:08:43Zoai:repositorio.unesp.br:11449/304126Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-01T05:08:43Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects
title Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects
spellingShingle Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects
Muñoz, Eladio
3D-printed scaffolds
additive manufacture
bone regeneration
hydroxyapatite
β-tricalcium phosphate
title_short Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects
title_full Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects
title_fullStr Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects
title_full_unstemmed Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects
title_sort Synthetic Bone Blocks Produced by Additive Manufacturing in the Repair of Critical Bone Defects
author Muñoz, Eladio
author_facet Muñoz, Eladio
Loyola, Ana Carolina
Pitol-Palin, Leticia [UNESP]
Okamoto, Roberta [UNESP]
Shibli, Jamil
Messora, Michel
Novaes, Arthur Belém
Scombatti de Souza, Sergio
author_role author
author2 Loyola, Ana Carolina
Pitol-Palin, Leticia [UNESP]
Okamoto, Roberta [UNESP]
Shibli, Jamil
Messora, Michel
Novaes, Arthur Belém
Scombatti de Souza, Sergio
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (UNESP)
Odontológicos e Correlatos S.A
Guarulhos University
dc.contributor.author.fl_str_mv Muñoz, Eladio
Loyola, Ana Carolina
Pitol-Palin, Leticia [UNESP]
Okamoto, Roberta [UNESP]
Shibli, Jamil
Messora, Michel
Novaes, Arthur Belém
Scombatti de Souza, Sergio
dc.subject.por.fl_str_mv 3D-printed scaffolds
additive manufacture
bone regeneration
hydroxyapatite
β-tricalcium phosphate
topic 3D-printed scaffolds
additive manufacture
bone regeneration
hydroxyapatite
β-tricalcium phosphate
description This study evaluated the efficacy of synthetic bone blocks, composed of hydroxyapatite (HA) or β-tricalcium phosphate (B-TCP), which were produced by additive manufacturing and used for the repair of critical size bone defects (CSDs) in rat calvaria. Sixty rats were divided into five groups (n = 12): blood clot (CONTROL), 3D-printed HA (HA), 3D-printed β-TCP (B-TCP), 3D-printed HA + autologous micrograft (HA+RIG), and 3D-printed β-TCP + autologous micrograft (B-TCP+RIG). CSDs were surgically created in the parietal bone and treated with the respective biomaterials. The animals were euthanized at 30 and 60 days postsurgery for microcomputed tomography (micro-CT) histomorphometric, and immunohistochemical analysis to assess new bone formation. Micro-CT analysis showed that both biomaterials were incorporated into the animals’ calvaria. The HA+RIG group, especially at 60 days, exhibited a significant increase in bone formation compared with the control. The use of 3D-printed bioceramics resulted in thinner trabeculae but a higher number of trabeculae compared with the control. Histomorphometric analysis showed bone islands in close contact with the B-TCP and HA blocks at 30 days. The HA blocks (HA and HA+RIG groups) showed statistically higher new bone formation values with further improvement when autologous micrografts were included. Immunohistochemical analysis showed the expression of bone repair proteins. At 30 days, the HA+RIG group had moderate Osteopontin (OPN) staining, indicating that the repair process had started, whereas other groups showed no staining. At 60 days, the HA+RIG group showed slight staining, similar to that of the control. Osteocalcin (OCN) staining, indicating osteoblastic activity, showed moderate expression in the HA and HA+RIG groups at 30 days, with slight expression in the B-TCP and B-TCP+RIG groups. The combination of HA blocks with autologous micrografts significantly enhanced bone repair, suggesting that the presence of progenitor cells and growth factors in the micrografts contributed to the improved outcomes. It was concluded that 3D-printed bone substitute blocks, associated with autologous micrografts, are highly effective in promoting bone repair in CSDs in rat calvaria.
publishDate 2024
dc.date.none.fl_str_mv 2024-11-01
2025-04-29T19:33:55Z
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/10.1089/ten.tec.2024.0214
Tissue Engineering - Part C: Methods, v. 30, n. 11, p. 533-546, 2024.
1937-3392
1937-3384
https://hdl.handle.net/11449/304126
10.1089/ten.tec.2024.0214
2-s2.0-85207119728
url http://dx.doi.org/10.1089/ten.tec.2024.0214
https://hdl.handle.net/11449/304126
identifier_str_mv Tissue Engineering - Part C: Methods, v. 30, n. 11, p. 533-546, 2024.
1937-3392
1937-3384
10.1089/ten.tec.2024.0214
2-s2.0-85207119728
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Tissue Engineering - Part C: Methods
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 533-546
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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