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In Vivo Validation of Spray-Dried Mesoporous Bioactive Glass Microspheres Acting as Prolonged Local Release Systems for BMP-2 to Support Bone Regeneration
Bone morphogenetic protein-2 (BMP-2) is a known key mediator of physiological bone regeneration and is clinically approved for selected musculoskeletal interventions. Yet, broad usage of this growth factor is impeded due to side effects that are majorly evoked by high dosages and burst release kinet...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559713/ https://www.ncbi.nlm.nih.gov/pubmed/32872353 http://dx.doi.org/10.3390/pharmaceutics12090823 |
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author | Berkmann, Julia C. Herrera Martin, Aaron X. Pontremoli, Carlotta Zheng, Kai Bucher, Christian H. Ellinghaus, Agnes Boccaccini, Aldo R. Fiorilli, Sonia Vitale Brovarone, Chiara Duda, Georg N. Schmidt-Bleek, Katharina |
author_facet | Berkmann, Julia C. Herrera Martin, Aaron X. Pontremoli, Carlotta Zheng, Kai Bucher, Christian H. Ellinghaus, Agnes Boccaccini, Aldo R. Fiorilli, Sonia Vitale Brovarone, Chiara Duda, Georg N. Schmidt-Bleek, Katharina |
author_sort | Berkmann, Julia C. |
collection | PubMed |
description | Bone morphogenetic protein-2 (BMP-2) is a known key mediator of physiological bone regeneration and is clinically approved for selected musculoskeletal interventions. Yet, broad usage of this growth factor is impeded due to side effects that are majorly evoked by high dosages and burst release kinetics. In this study, mesoporous bioactive glass microspheres (MBGs), produced by an aerosol-assisted spray-drying scalable process, were loaded with BMP-2 resulting in prolonged, low-dose BMP-2 release without affecting the material characteristics. In vitro, MBGs were found to be cytocompatible and to induce a pro-osteogenic response in primary human mesenchymal stromal cells (MSCs). In a pre-clinical rodent model, BMP-2 loaded MBGs significantly enhanced bone formation and influenced the microarchitecture of newly formed bone. The MBG carriers alone performed equal to the untreated (empty) control in most parameters tested, while additionally exerting mild pro-angiogenic effects. Using MBGs as a biocompatible, pro-regenerative carrier for local and sustained low dose BMP-2 release could limit side effects, thus enabling a safer usage of BMP-2 as a potent pro-osteogenic growth factor. |
format | Online Article Text |
id | pubmed-7559713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75597132020-10-29 In Vivo Validation of Spray-Dried Mesoporous Bioactive Glass Microspheres Acting as Prolonged Local Release Systems for BMP-2 to Support Bone Regeneration Berkmann, Julia C. Herrera Martin, Aaron X. Pontremoli, Carlotta Zheng, Kai Bucher, Christian H. Ellinghaus, Agnes Boccaccini, Aldo R. Fiorilli, Sonia Vitale Brovarone, Chiara Duda, Georg N. Schmidt-Bleek, Katharina Pharmaceutics Article Bone morphogenetic protein-2 (BMP-2) is a known key mediator of physiological bone regeneration and is clinically approved for selected musculoskeletal interventions. Yet, broad usage of this growth factor is impeded due to side effects that are majorly evoked by high dosages and burst release kinetics. In this study, mesoporous bioactive glass microspheres (MBGs), produced by an aerosol-assisted spray-drying scalable process, were loaded with BMP-2 resulting in prolonged, low-dose BMP-2 release without affecting the material characteristics. In vitro, MBGs were found to be cytocompatible and to induce a pro-osteogenic response in primary human mesenchymal stromal cells (MSCs). In a pre-clinical rodent model, BMP-2 loaded MBGs significantly enhanced bone formation and influenced the microarchitecture of newly formed bone. The MBG carriers alone performed equal to the untreated (empty) control in most parameters tested, while additionally exerting mild pro-angiogenic effects. Using MBGs as a biocompatible, pro-regenerative carrier for local and sustained low dose BMP-2 release could limit side effects, thus enabling a safer usage of BMP-2 as a potent pro-osteogenic growth factor. MDPI 2020-08-28 /pmc/articles/PMC7559713/ /pubmed/32872353 http://dx.doi.org/10.3390/pharmaceutics12090823 Text en © 2020 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 Berkmann, Julia C. Herrera Martin, Aaron X. Pontremoli, Carlotta Zheng, Kai Bucher, Christian H. Ellinghaus, Agnes Boccaccini, Aldo R. Fiorilli, Sonia Vitale Brovarone, Chiara Duda, Georg N. Schmidt-Bleek, Katharina In Vivo Validation of Spray-Dried Mesoporous Bioactive Glass Microspheres Acting as Prolonged Local Release Systems for BMP-2 to Support Bone Regeneration |
title | In Vivo Validation of Spray-Dried Mesoporous Bioactive Glass Microspheres Acting as Prolonged Local Release Systems for BMP-2 to Support Bone Regeneration |
title_full | In Vivo Validation of Spray-Dried Mesoporous Bioactive Glass Microspheres Acting as Prolonged Local Release Systems for BMP-2 to Support Bone Regeneration |
title_fullStr | In Vivo Validation of Spray-Dried Mesoporous Bioactive Glass Microspheres Acting as Prolonged Local Release Systems for BMP-2 to Support Bone Regeneration |
title_full_unstemmed | In Vivo Validation of Spray-Dried Mesoporous Bioactive Glass Microspheres Acting as Prolonged Local Release Systems for BMP-2 to Support Bone Regeneration |
title_short | In Vivo Validation of Spray-Dried Mesoporous Bioactive Glass Microspheres Acting as Prolonged Local Release Systems for BMP-2 to Support Bone Regeneration |
title_sort | in vivo validation of spray-dried mesoporous bioactive glass microspheres acting as prolonged local release systems for bmp-2 to support bone regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559713/ https://www.ncbi.nlm.nih.gov/pubmed/32872353 http://dx.doi.org/10.3390/pharmaceutics12090823 |
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