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A Comparative Study of HA/DBM Compounds Derived from Bovine and Porcine for Bone Regeneration

This comparative study investigated the tissue regeneration and inflammatory response induced by xenografts comprised of hydroxyapatite (HA) and demineralized bone matrix (DBM) extracted from porcine (P) and bovine (B) sources. First, extraction of HA and DBM was independently conducted, followed by...

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Autores principales: Roldan, Lina, Isaza, Catalina, Ospina, Juan, Montoya, Carolina, Domínguez, José, Orrego, Santiago, Correa, Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532284/
https://www.ncbi.nlm.nih.gov/pubmed/37754853
http://dx.doi.org/10.3390/jfb14090439
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author Roldan, Lina
Isaza, Catalina
Ospina, Juan
Montoya, Carolina
Domínguez, José
Orrego, Santiago
Correa, Santiago
author_facet Roldan, Lina
Isaza, Catalina
Ospina, Juan
Montoya, Carolina
Domínguez, José
Orrego, Santiago
Correa, Santiago
author_sort Roldan, Lina
collection PubMed
description This comparative study investigated the tissue regeneration and inflammatory response induced by xenografts comprised of hydroxyapatite (HA) and demineralized bone matrix (DBM) extracted from porcine (P) and bovine (B) sources. First, extraction of HA and DBM was independently conducted, followed by chemical and morphological characterization. Second, mixtures of HA/DBM were prepared in 50/50 and 60/40 concentrations, and the chemical, morphological, and mechanical properties were evaluated. A rat calvarial defect model was used to evaluate the tissue regeneration and inflammatory responses at 3 and 6 months. The commercial allograft DBM Puros(®) was used as a clinical reference. Different variables related to tissue regeneration were evaluated, including tissue thickness regeneration (%), amount of regenerated bone area (%), and amount of regenerated collagen area (%). The inflammatory response was evaluated by quantifying the blood vessel area. Overall, tissue regeneration from porcine grafts was superior to bovine. After 3 months of implantation, the tissue thickness regeneration in the 50/50P compound and the commercial DBM was significantly higher (~99%) than in the bovine materials (~23%). The 50/50P and DBM produced higher tissue regeneration than the naturally healed controls. Similar trends were observed for the regenerated bone and collagen areas. The blood vessel area was correlated with tissue regeneration in the first 3 months of evaluation. After 6 months of implantation, HA/DBM compounds showed less regenerated collagen than the DBM-only xenografts. In addition, all animal-derived xenografts improved tissue regeneration compared with the naturally healed defects. No clinical complications associated with any implanted compound were noted.
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spelling pubmed-105322842023-09-28 A Comparative Study of HA/DBM Compounds Derived from Bovine and Porcine for Bone Regeneration Roldan, Lina Isaza, Catalina Ospina, Juan Montoya, Carolina Domínguez, José Orrego, Santiago Correa, Santiago J Funct Biomater Article This comparative study investigated the tissue regeneration and inflammatory response induced by xenografts comprised of hydroxyapatite (HA) and demineralized bone matrix (DBM) extracted from porcine (P) and bovine (B) sources. First, extraction of HA and DBM was independently conducted, followed by chemical and morphological characterization. Second, mixtures of HA/DBM were prepared in 50/50 and 60/40 concentrations, and the chemical, morphological, and mechanical properties were evaluated. A rat calvarial defect model was used to evaluate the tissue regeneration and inflammatory responses at 3 and 6 months. The commercial allograft DBM Puros(®) was used as a clinical reference. Different variables related to tissue regeneration were evaluated, including tissue thickness regeneration (%), amount of regenerated bone area (%), and amount of regenerated collagen area (%). The inflammatory response was evaluated by quantifying the blood vessel area. Overall, tissue regeneration from porcine grafts was superior to bovine. After 3 months of implantation, the tissue thickness regeneration in the 50/50P compound and the commercial DBM was significantly higher (~99%) than in the bovine materials (~23%). The 50/50P and DBM produced higher tissue regeneration than the naturally healed controls. Similar trends were observed for the regenerated bone and collagen areas. The blood vessel area was correlated with tissue regeneration in the first 3 months of evaluation. After 6 months of implantation, HA/DBM compounds showed less regenerated collagen than the DBM-only xenografts. In addition, all animal-derived xenografts improved tissue regeneration compared with the naturally healed defects. No clinical complications associated with any implanted compound were noted. MDPI 2023-08-24 /pmc/articles/PMC10532284/ /pubmed/37754853 http://dx.doi.org/10.3390/jfb14090439 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Roldan, Lina
Isaza, Catalina
Ospina, Juan
Montoya, Carolina
Domínguez, José
Orrego, Santiago
Correa, Santiago
A Comparative Study of HA/DBM Compounds Derived from Bovine and Porcine for Bone Regeneration
title A Comparative Study of HA/DBM Compounds Derived from Bovine and Porcine for Bone Regeneration
title_full A Comparative Study of HA/DBM Compounds Derived from Bovine and Porcine for Bone Regeneration
title_fullStr A Comparative Study of HA/DBM Compounds Derived from Bovine and Porcine for Bone Regeneration
title_full_unstemmed A Comparative Study of HA/DBM Compounds Derived from Bovine and Porcine for Bone Regeneration
title_short A Comparative Study of HA/DBM Compounds Derived from Bovine and Porcine for Bone Regeneration
title_sort comparative study of ha/dbm compounds derived from bovine and porcine for bone regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532284/
https://www.ncbi.nlm.nih.gov/pubmed/37754853
http://dx.doi.org/10.3390/jfb14090439
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