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Sequential dual-drug delivery of BMP-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration
The clinical use of bioactive molecules in bone regeneration has been known to have side effects, which result from uncontrolled and supraphysiological doses. In this study, we demonstrated the synergistic effect of two bioactive molecules, bone morphogenic protein-2 (BMP-2) and alendronate (ALN), b...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804460/ https://www.ncbi.nlm.nih.gov/pubmed/33436904 http://dx.doi.org/10.1038/s41598-020-80608-3 |
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author | Lee, Dongtak Wufuer, Maierdanjiang Kim, Insu Choi, Tae Hyun Kim, Byung Jun Jung, Hyo Gi Jeon, Byoungjun Lee, Gyudo Jeon, Ok Hee Chang, Hak Yoon, Dae Sung |
author_facet | Lee, Dongtak Wufuer, Maierdanjiang Kim, Insu Choi, Tae Hyun Kim, Byung Jun Jung, Hyo Gi Jeon, Byoungjun Lee, Gyudo Jeon, Ok Hee Chang, Hak Yoon, Dae Sung |
author_sort | Lee, Dongtak |
collection | PubMed |
description | The clinical use of bioactive molecules in bone regeneration has been known to have side effects, which result from uncontrolled and supraphysiological doses. In this study, we demonstrated the synergistic effect of two bioactive molecules, bone morphogenic protein-2 (BMP-2) and alendronate (ALN), by releasing them in a sequential manner. Collagen-hydroxyapatite composite scaffolds functionalized using BMP-2 are loaded with biodegradable microspheres where ALN is encapsulated. The results indicate an initial release of BMP-2 for a few days, followed by the sequential release of ALN after two weeks. The composite scaffolds significantly increase osteogenic activity owing to the synergistic effect of BMP-2 and ALN. Enhanced bone regeneration was identified at eight weeks post-implantation in the rat 8-mm critical-sized defect. Our findings suggest that the sequential delivery of BMP-2 and ALN from the scaffolds results in a synergistic effect on bone regeneration, which is unprecedented. Therefore, such a system exhibits potential for the application of cell-free tissue engineering. |
format | Online Article Text |
id | pubmed-7804460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78044602021-01-13 Sequential dual-drug delivery of BMP-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration Lee, Dongtak Wufuer, Maierdanjiang Kim, Insu Choi, Tae Hyun Kim, Byung Jun Jung, Hyo Gi Jeon, Byoungjun Lee, Gyudo Jeon, Ok Hee Chang, Hak Yoon, Dae Sung Sci Rep Article The clinical use of bioactive molecules in bone regeneration has been known to have side effects, which result from uncontrolled and supraphysiological doses. In this study, we demonstrated the synergistic effect of two bioactive molecules, bone morphogenic protein-2 (BMP-2) and alendronate (ALN), by releasing them in a sequential manner. Collagen-hydroxyapatite composite scaffolds functionalized using BMP-2 are loaded with biodegradable microspheres where ALN is encapsulated. The results indicate an initial release of BMP-2 for a few days, followed by the sequential release of ALN after two weeks. The composite scaffolds significantly increase osteogenic activity owing to the synergistic effect of BMP-2 and ALN. Enhanced bone regeneration was identified at eight weeks post-implantation in the rat 8-mm critical-sized defect. Our findings suggest that the sequential delivery of BMP-2 and ALN from the scaffolds results in a synergistic effect on bone regeneration, which is unprecedented. Therefore, such a system exhibits potential for the application of cell-free tissue engineering. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7804460/ /pubmed/33436904 http://dx.doi.org/10.1038/s41598-020-80608-3 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lee, Dongtak Wufuer, Maierdanjiang Kim, Insu Choi, Tae Hyun Kim, Byung Jun Jung, Hyo Gi Jeon, Byoungjun Lee, Gyudo Jeon, Ok Hee Chang, Hak Yoon, Dae Sung Sequential dual-drug delivery of BMP-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration |
title | Sequential dual-drug delivery of BMP-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration |
title_full | Sequential dual-drug delivery of BMP-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration |
title_fullStr | Sequential dual-drug delivery of BMP-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration |
title_full_unstemmed | Sequential dual-drug delivery of BMP-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration |
title_short | Sequential dual-drug delivery of BMP-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration |
title_sort | sequential dual-drug delivery of bmp-2 and alendronate from hydroxyapatite-collagen scaffolds for enhanced bone regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804460/ https://www.ncbi.nlm.nih.gov/pubmed/33436904 http://dx.doi.org/10.1038/s41598-020-80608-3 |
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