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Stimulation of Bone Healing by Sustained Bone Morphogenetic Protein 2 (BMP-2) Delivery
The aim of the study was to investigate the effect of a sustained release of bone morphogenetic protein2 (BMP-2) incorporated in a polymeric implant coating on bone healing. In vitro analysis revealed a sustained, but incomplete BMP-2 release until Day 42. For the in vivo study, the rat tibia osteot...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057747/ https://www.ncbi.nlm.nih.gov/pubmed/24830556 http://dx.doi.org/10.3390/ijms15058539 |
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author | Faßbender, Mirja Minkwitz, Susann Strobel, Catrin Schmidmaier, Gerhard Wildemann, Britt |
author_facet | Faßbender, Mirja Minkwitz, Susann Strobel, Catrin Schmidmaier, Gerhard Wildemann, Britt |
author_sort | Faßbender, Mirja |
collection | PubMed |
description | The aim of the study was to investigate the effect of a sustained release of bone morphogenetic protein2 (BMP-2) incorporated in a polymeric implant coating on bone healing. In vitro analysis revealed a sustained, but incomplete BMP-2 release until Day 42. For the in vivo study, the rat tibia osteotomy was stabilized either with control or BMP-2 coated wires, and the healing progress was followed by micro computed tomography (μCT), biomechanical testing and histology at Days 10, 28, 42 and 84. MicroCT showed an accelerated formation of mineralized callus, as well as remodeling and an increase of mineralized/total callus volume (p = 0.021) at Day 42 in the BMP-2 group compared to the control. Histology revealed an increased callus mineralization at Days 42 and 84 (p = 0.006) with reduced cartilage at Day 84 (p = 0.004) in the BMP-2 group. Biomechanical stiffness was significantly higher in the BMP-2 group (p = 0.045) at Day 42. In summary, bone healing was enhanced after sustained BMP-2 application compared to the control. Using the same drug delivery system, but a burst release of BMP-2, a previous published study showed a similar positive effect on bone healing. Distinct differences in the healing outcome might be explained due to the different BMP release kinetics and dosages. However, further studies are necessary to adapt the optimal release profiles to physiological mechanisms. |
format | Online Article Text |
id | pubmed-4057747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-40577472014-06-16 Stimulation of Bone Healing by Sustained Bone Morphogenetic Protein 2 (BMP-2) Delivery Faßbender, Mirja Minkwitz, Susann Strobel, Catrin Schmidmaier, Gerhard Wildemann, Britt Int J Mol Sci Article The aim of the study was to investigate the effect of a sustained release of bone morphogenetic protein2 (BMP-2) incorporated in a polymeric implant coating on bone healing. In vitro analysis revealed a sustained, but incomplete BMP-2 release until Day 42. For the in vivo study, the rat tibia osteotomy was stabilized either with control or BMP-2 coated wires, and the healing progress was followed by micro computed tomography (μCT), biomechanical testing and histology at Days 10, 28, 42 and 84. MicroCT showed an accelerated formation of mineralized callus, as well as remodeling and an increase of mineralized/total callus volume (p = 0.021) at Day 42 in the BMP-2 group compared to the control. Histology revealed an increased callus mineralization at Days 42 and 84 (p = 0.006) with reduced cartilage at Day 84 (p = 0.004) in the BMP-2 group. Biomechanical stiffness was significantly higher in the BMP-2 group (p = 0.045) at Day 42. In summary, bone healing was enhanced after sustained BMP-2 application compared to the control. Using the same drug delivery system, but a burst release of BMP-2, a previous published study showed a similar positive effect on bone healing. Distinct differences in the healing outcome might be explained due to the different BMP release kinetics and dosages. However, further studies are necessary to adapt the optimal release profiles to physiological mechanisms. Molecular Diversity Preservation International (MDPI) 2014-05-14 /pmc/articles/PMC4057747/ /pubmed/24830556 http://dx.doi.org/10.3390/ijms15058539 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Faßbender, Mirja Minkwitz, Susann Strobel, Catrin Schmidmaier, Gerhard Wildemann, Britt Stimulation of Bone Healing by Sustained Bone Morphogenetic Protein 2 (BMP-2) Delivery |
title | Stimulation of Bone Healing by Sustained Bone Morphogenetic Protein 2 (BMP-2) Delivery |
title_full | Stimulation of Bone Healing by Sustained Bone Morphogenetic Protein 2 (BMP-2) Delivery |
title_fullStr | Stimulation of Bone Healing by Sustained Bone Morphogenetic Protein 2 (BMP-2) Delivery |
title_full_unstemmed | Stimulation of Bone Healing by Sustained Bone Morphogenetic Protein 2 (BMP-2) Delivery |
title_short | Stimulation of Bone Healing by Sustained Bone Morphogenetic Protein 2 (BMP-2) Delivery |
title_sort | stimulation of bone healing by sustained bone morphogenetic protein 2 (bmp-2) delivery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057747/ https://www.ncbi.nlm.nih.gov/pubmed/24830556 http://dx.doi.org/10.3390/ijms15058539 |
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