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Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model
Large bone defects pose an unsolved challenge for orthopedic surgeons. Our group has previously reported the construction of a barrier membrane made of ammoniomethacrylate copolymer USP (AMCA), which supports the adhesion, proliferation, and osteoblastic differentiation of human mesenchymal stem cel...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603551/ https://www.ncbi.nlm.nih.gov/pubmed/33150177 http://dx.doi.org/10.1155/2020/5905740 |
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author | Kirmayer, David Grin, Ada Gefter (Shenderovich), Julia Friedman, Michael Rachmilewitz, Jacob Mosheiff, Rami Kenett, Ron Khoury, Amal |
author_facet | Kirmayer, David Grin, Ada Gefter (Shenderovich), Julia Friedman, Michael Rachmilewitz, Jacob Mosheiff, Rami Kenett, Ron Khoury, Amal |
author_sort | Kirmayer, David |
collection | PubMed |
description | Large bone defects pose an unsolved challenge for orthopedic surgeons. Our group has previously reported the construction of a barrier membrane made of ammoniomethacrylate copolymer USP (AMCA), which supports the adhesion, proliferation, and osteoblastic differentiation of human mesenchymal stem cells (hMSCs). In this study, we report the use of AMCA membranes to seclude critical segmental defect (~1.0 cm) created in the middle third of rabbit radius and test the efficiency of bone regeneration. Bone regeneration was assessed by radiography, biweekly for 8 weeks. The results were verified by histology and micro-CT at the end of the follow-up. The AMCA membranes were found superior to no treatment in terms of new bone formation in the defect, bone volume, callus surface area normalized to total volume, and the number of bone trabeculae, after eight weeks. Additional factors were then assessed, and these included the addition of simvastatin to the membrane, coating the membrane with human MSC, and a combination of those. The addition of simvastatin to the membranes demonstrated a stronger effect at a similar radiological follow-up. We conclude that AMCA barrier membranes per se and simvastatin delivered in a controlled manner improve bone regeneration outcome. |
format | Online Article Text |
id | pubmed-7603551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-76035512020-11-03 Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model Kirmayer, David Grin, Ada Gefter (Shenderovich), Julia Friedman, Michael Rachmilewitz, Jacob Mosheiff, Rami Kenett, Ron Khoury, Amal Biomed Res Int Research Article Large bone defects pose an unsolved challenge for orthopedic surgeons. Our group has previously reported the construction of a barrier membrane made of ammoniomethacrylate copolymer USP (AMCA), which supports the adhesion, proliferation, and osteoblastic differentiation of human mesenchymal stem cells (hMSCs). In this study, we report the use of AMCA membranes to seclude critical segmental defect (~1.0 cm) created in the middle third of rabbit radius and test the efficiency of bone regeneration. Bone regeneration was assessed by radiography, biweekly for 8 weeks. The results were verified by histology and micro-CT at the end of the follow-up. The AMCA membranes were found superior to no treatment in terms of new bone formation in the defect, bone volume, callus surface area normalized to total volume, and the number of bone trabeculae, after eight weeks. Additional factors were then assessed, and these included the addition of simvastatin to the membrane, coating the membrane with human MSC, and a combination of those. The addition of simvastatin to the membranes demonstrated a stronger effect at a similar radiological follow-up. We conclude that AMCA barrier membranes per se and simvastatin delivered in a controlled manner improve bone regeneration outcome. Hindawi 2020-10-13 /pmc/articles/PMC7603551/ /pubmed/33150177 http://dx.doi.org/10.1155/2020/5905740 Text en Copyright © 2020 David Kirmayer et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kirmayer, David Grin, Ada Gefter (Shenderovich), Julia Friedman, Michael Rachmilewitz, Jacob Mosheiff, Rami Kenett, Ron Khoury, Amal Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model |
title | Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model |
title_full | Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model |
title_fullStr | Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model |
title_full_unstemmed | Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model |
title_short | Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model |
title_sort | guided bone regeneration with ammoniomethacrylate-based barrier membranes in a radial defect model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603551/ https://www.ncbi.nlm.nih.gov/pubmed/33150177 http://dx.doi.org/10.1155/2020/5905740 |
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