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Loading BMP-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration
INTRODUCTION: Tissue engineering is a promising strategy for bone regeneration in repairing massive bone defects. The surface morphology of implanted materials plays a key role in bone healing; these materials incorporate osteoinductive factors to improve the efficiency of bone regeneration. MATERIA...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047624/ https://www.ncbi.nlm.nih.gov/pubmed/30034234 http://dx.doi.org/10.2147/IJN.S158280 |
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author | Zhou, Panyu Wu, Jianghong Xia, Yan Yuan, Ye Zhang, Hongyue Xu, Shuogui Lin, Kaili |
author_facet | Zhou, Panyu Wu, Jianghong Xia, Yan Yuan, Ye Zhang, Hongyue Xu, Shuogui Lin, Kaili |
author_sort | Zhou, Panyu |
collection | PubMed |
description | INTRODUCTION: Tissue engineering is a promising strategy for bone regeneration in repairing massive bone defects. The surface morphology of implanted materials plays a key role in bone healing; these materials incorporate osteoinductive factors to improve the efficiency of bone regeneration. MATERIALS AND METHODS: In the current study, nanostructured hydroxyapatite (nHAp) micro-spheres were prepared via a hydrothermal transformation method using calcium silicate (CS) microspheres as precursors; the CS microspheres were obtained by a spray-drying method. The nHAp microspheres constructed by the nano-whiskers significantly improved the ability of the microspheres to adsorb the bioactive protein (BMP-2) and reduce its initial burst release. To evaluate the in vivo bone regeneration of microspheres, both conventional hydroxyapatite (HAp) and nHAp microspheres were either loaded with recombinant human bone morphogenetic protein-2 (rhBMP-2) or not loaded with the protein; these microspheres were implanted in rat femoral bone defects for 4 and 8 weeks. RESULTS AND DISCUSSION: The results of our three-dimensional (3D) micro-computed tomography (CT) and histomorphometric observations showed that the combination of the nano-structured surface and rhBMP-2 obviously improved osteogenesis compared to conventional HAp microspheres loaded with rhBMP-2. Our results suggest that the nHAp microspheres with a nanostructured surface adsorb rhBMP-2 for rapid bone formation; they therefore show the potential to act as carriers in bone tissue regeneration. |
format | Online Article Text |
id | pubmed-6047624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60476242018-07-20 Loading BMP-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration Zhou, Panyu Wu, Jianghong Xia, Yan Yuan, Ye Zhang, Hongyue Xu, Shuogui Lin, Kaili Int J Nanomedicine Original Research INTRODUCTION: Tissue engineering is a promising strategy for bone regeneration in repairing massive bone defects. The surface morphology of implanted materials plays a key role in bone healing; these materials incorporate osteoinductive factors to improve the efficiency of bone regeneration. MATERIALS AND METHODS: In the current study, nanostructured hydroxyapatite (nHAp) micro-spheres were prepared via a hydrothermal transformation method using calcium silicate (CS) microspheres as precursors; the CS microspheres were obtained by a spray-drying method. The nHAp microspheres constructed by the nano-whiskers significantly improved the ability of the microspheres to adsorb the bioactive protein (BMP-2) and reduce its initial burst release. To evaluate the in vivo bone regeneration of microspheres, both conventional hydroxyapatite (HAp) and nHAp microspheres were either loaded with recombinant human bone morphogenetic protein-2 (rhBMP-2) or not loaded with the protein; these microspheres were implanted in rat femoral bone defects for 4 and 8 weeks. RESULTS AND DISCUSSION: The results of our three-dimensional (3D) micro-computed tomography (CT) and histomorphometric observations showed that the combination of the nano-structured surface and rhBMP-2 obviously improved osteogenesis compared to conventional HAp microspheres loaded with rhBMP-2. Our results suggest that the nHAp microspheres with a nanostructured surface adsorb rhBMP-2 for rapid bone formation; they therefore show the potential to act as carriers in bone tissue regeneration. Dove Medical Press 2018-07-11 /pmc/articles/PMC6047624/ /pubmed/30034234 http://dx.doi.org/10.2147/IJN.S158280 Text en © 2018 Zhou et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zhou, Panyu Wu, Jianghong Xia, Yan Yuan, Ye Zhang, Hongyue Xu, Shuogui Lin, Kaili Loading BMP-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration |
title | Loading BMP-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration |
title_full | Loading BMP-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration |
title_fullStr | Loading BMP-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration |
title_full_unstemmed | Loading BMP-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration |
title_short | Loading BMP-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration |
title_sort | loading bmp-2 on nanostructured hydroxyapatite microspheres for rapid bone regeneration |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047624/ https://www.ncbi.nlm.nih.gov/pubmed/30034234 http://dx.doi.org/10.2147/IJN.S158280 |
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