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Collagen-Based Matrices for Osteoconduction: A Preclinical In Vivo Study

The aim of this study was to evaluate the influence of additional hydroxyapatite (HA) in collagen-based matrices (CM) and membrane placement on bone formation in calvarial defects. Critical size defects in the calvaria of 16 New Zealand White Rabbits were randomly treated with CM or mineralized coll...

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Autores principales: Katagiri, Hiroki, El Tawil, Yacine, Lang, Niklaus P., Imber, Jean-Claude, Sculean, Anton, Fujioka-Kobayashi, Masako, Saulacic, Nikola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913003/
https://www.ncbi.nlm.nih.gov/pubmed/33540647
http://dx.doi.org/10.3390/biomedicines9020143
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author Katagiri, Hiroki
El Tawil, Yacine
Lang, Niklaus P.
Imber, Jean-Claude
Sculean, Anton
Fujioka-Kobayashi, Masako
Saulacic, Nikola
author_facet Katagiri, Hiroki
El Tawil, Yacine
Lang, Niklaus P.
Imber, Jean-Claude
Sculean, Anton
Fujioka-Kobayashi, Masako
Saulacic, Nikola
author_sort Katagiri, Hiroki
collection PubMed
description The aim of this study was to evaluate the influence of additional hydroxyapatite (HA) in collagen-based matrices (CM) and membrane placement on bone formation in calvarial defects. Critical size defects in the calvaria of 16 New Zealand White Rabbits were randomly treated with CM or mineralized collagen-based matrices (mCM). Half of the sites were covered with a collagen membrane. Animals were euthanized after 12 weeks of healing. The samples were studied by micro-CT and histology. Newly formed lamellar bone was observed in all samples at the periphery of the defect. In the central areas, however, new bone composed of both woven and lamellar bone was embedded in the soft tissue. Samples treated with mCM showed more residual biomaterial and induced more small bony islands in the central areas of the defects than samples with CM. Nevertheless, a complete defect closure was not observed in any of the samples at 12 weeks. Membrane placement resulted in a decrease in bone density and height. Significant differences between the groups were revealed only between CM groups with and without membrane coverage for bone height in the central area of the defect. Neither mineralization of CM nor membrane placement improved the osteogenic capacity in this particular defect. Nevertheless, mineralisation influenced bone density without a membrane placement and bone volume underneath a membrane. CM may be used as a scaffold in bone regeneration procedures, without the need of a membrane coverage. Further preclinical studies are warrant to optimise the potential of mCM.
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spelling pubmed-79130032021-02-28 Collagen-Based Matrices for Osteoconduction: A Preclinical In Vivo Study Katagiri, Hiroki El Tawil, Yacine Lang, Niklaus P. Imber, Jean-Claude Sculean, Anton Fujioka-Kobayashi, Masako Saulacic, Nikola Biomedicines Article The aim of this study was to evaluate the influence of additional hydroxyapatite (HA) in collagen-based matrices (CM) and membrane placement on bone formation in calvarial defects. Critical size defects in the calvaria of 16 New Zealand White Rabbits were randomly treated with CM or mineralized collagen-based matrices (mCM). Half of the sites were covered with a collagen membrane. Animals were euthanized after 12 weeks of healing. The samples were studied by micro-CT and histology. Newly formed lamellar bone was observed in all samples at the periphery of the defect. In the central areas, however, new bone composed of both woven and lamellar bone was embedded in the soft tissue. Samples treated with mCM showed more residual biomaterial and induced more small bony islands in the central areas of the defects than samples with CM. Nevertheless, a complete defect closure was not observed in any of the samples at 12 weeks. Membrane placement resulted in a decrease in bone density and height. Significant differences between the groups were revealed only between CM groups with and without membrane coverage for bone height in the central area of the defect. Neither mineralization of CM nor membrane placement improved the osteogenic capacity in this particular defect. Nevertheless, mineralisation influenced bone density without a membrane placement and bone volume underneath a membrane. CM may be used as a scaffold in bone regeneration procedures, without the need of a membrane coverage. Further preclinical studies are warrant to optimise the potential of mCM. MDPI 2021-02-02 /pmc/articles/PMC7913003/ /pubmed/33540647 http://dx.doi.org/10.3390/biomedicines9020143 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Katagiri, Hiroki
El Tawil, Yacine
Lang, Niklaus P.
Imber, Jean-Claude
Sculean, Anton
Fujioka-Kobayashi, Masako
Saulacic, Nikola
Collagen-Based Matrices for Osteoconduction: A Preclinical In Vivo Study
title Collagen-Based Matrices for Osteoconduction: A Preclinical In Vivo Study
title_full Collagen-Based Matrices for Osteoconduction: A Preclinical In Vivo Study
title_fullStr Collagen-Based Matrices for Osteoconduction: A Preclinical In Vivo Study
title_full_unstemmed Collagen-Based Matrices for Osteoconduction: A Preclinical In Vivo Study
title_short Collagen-Based Matrices for Osteoconduction: A Preclinical In Vivo Study
title_sort collagen-based matrices for osteoconduction: a preclinical in vivo study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913003/
https://www.ncbi.nlm.nih.gov/pubmed/33540647
http://dx.doi.org/10.3390/biomedicines9020143
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