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Repair of Cranial Bone Defects Using rhBMP2 and Submicron Particle of Biphasic Calcium Phosphate Ceramics with Through-Hole

Recently a submicron particle of biphasic calcium phosphate ceramic (BCP) with through-hole (donut-shaped BCP (d-BCP)) was developed for improving the osteoconductivity. This study was performed to examine the usefulness of d-BCP for the delivery of osteoinductive rhBMP2 and the effectiveness on cra...

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Autores principales: Jeong, Byung-Chul, Choi, Hyuck, Hur, Sung-Woong, Kim, Jung-Woo, Oh, Sin-Hye, Kim, Hyun-Seung, Song, Soo-Chang, Lee, Keun-Bae, Park, Kwang-Bum, Koh, Jeong-Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600556/
https://www.ncbi.nlm.nih.gov/pubmed/26491693
http://dx.doi.org/10.1155/2015/926291
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author Jeong, Byung-Chul
Choi, Hyuck
Hur, Sung-Woong
Kim, Jung-Woo
Oh, Sin-Hye
Kim, Hyun-Seung
Song, Soo-Chang
Lee, Keun-Bae
Park, Kwang-Bum
Koh, Jeong-Tae
author_facet Jeong, Byung-Chul
Choi, Hyuck
Hur, Sung-Woong
Kim, Jung-Woo
Oh, Sin-Hye
Kim, Hyun-Seung
Song, Soo-Chang
Lee, Keun-Bae
Park, Kwang-Bum
Koh, Jeong-Tae
author_sort Jeong, Byung-Chul
collection PubMed
description Recently a submicron particle of biphasic calcium phosphate ceramic (BCP) with through-hole (donut-shaped BCP (d-BCP)) was developed for improving the osteoconductivity. This study was performed to examine the usefulness of d-BCP for the delivery of osteoinductive rhBMP2 and the effectiveness on cranial bone regeneration. The d-BCP was soaked in rhBMP2 solution and then freeze-dried. Scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), and Raman spectroscopy analyses confirmed that rhBMP2 was well delivered onto the d-BCP surface and the through-hole. The bioactivity of the rhBMP2/d-BCP composite was validated in MC3T3-E1 cells as an in vitro model and in critical-sized cranial defects in C57BL/6 mice. When freeze-dried d-BCPs with rhBMP2 were placed in transwell inserts and suspended above MC3T3-E1, alkaline phosphatase activity and osteoblast-specific gene expression were increased compared to non-rhBMP2-containing d-BCPs. For evaluating in vivo effectiveness, freeze-dried d-BCPs with or without rhBMP2 were implanted into critical-sized cranial defects. Microcomputed tomography and histologic analysis showed that rhBMP2-containing d-BCPs significantly enhanced cranial bone regeneration compared to non-rhBMP2-containing control. These results suggest that a combination of d-BCP and rhBMP2 can accelerate bone regeneration, and this could be used to develop therapeutic strategies in hard tissue healing.
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spelling pubmed-46005562015-10-21 Repair of Cranial Bone Defects Using rhBMP2 and Submicron Particle of Biphasic Calcium Phosphate Ceramics with Through-Hole Jeong, Byung-Chul Choi, Hyuck Hur, Sung-Woong Kim, Jung-Woo Oh, Sin-Hye Kim, Hyun-Seung Song, Soo-Chang Lee, Keun-Bae Park, Kwang-Bum Koh, Jeong-Tae Biomed Res Int Research Article Recently a submicron particle of biphasic calcium phosphate ceramic (BCP) with through-hole (donut-shaped BCP (d-BCP)) was developed for improving the osteoconductivity. This study was performed to examine the usefulness of d-BCP for the delivery of osteoinductive rhBMP2 and the effectiveness on cranial bone regeneration. The d-BCP was soaked in rhBMP2 solution and then freeze-dried. Scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), and Raman spectroscopy analyses confirmed that rhBMP2 was well delivered onto the d-BCP surface and the through-hole. The bioactivity of the rhBMP2/d-BCP composite was validated in MC3T3-E1 cells as an in vitro model and in critical-sized cranial defects in C57BL/6 mice. When freeze-dried d-BCPs with rhBMP2 were placed in transwell inserts and suspended above MC3T3-E1, alkaline phosphatase activity and osteoblast-specific gene expression were increased compared to non-rhBMP2-containing d-BCPs. For evaluating in vivo effectiveness, freeze-dried d-BCPs with or without rhBMP2 were implanted into critical-sized cranial defects. Microcomputed tomography and histologic analysis showed that rhBMP2-containing d-BCPs significantly enhanced cranial bone regeneration compared to non-rhBMP2-containing control. These results suggest that a combination of d-BCP and rhBMP2 can accelerate bone regeneration, and this could be used to develop therapeutic strategies in hard tissue healing. Hindawi Publishing Corporation 2015 2015-09-27 /pmc/articles/PMC4600556/ /pubmed/26491693 http://dx.doi.org/10.1155/2015/926291 Text en Copyright © 2015 Byung-Chul Jeong et al. https://creativecommons.org/licenses/by/3.0/ 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
Jeong, Byung-Chul
Choi, Hyuck
Hur, Sung-Woong
Kim, Jung-Woo
Oh, Sin-Hye
Kim, Hyun-Seung
Song, Soo-Chang
Lee, Keun-Bae
Park, Kwang-Bum
Koh, Jeong-Tae
Repair of Cranial Bone Defects Using rhBMP2 and Submicron Particle of Biphasic Calcium Phosphate Ceramics with Through-Hole
title Repair of Cranial Bone Defects Using rhBMP2 and Submicron Particle of Biphasic Calcium Phosphate Ceramics with Through-Hole
title_full Repair of Cranial Bone Defects Using rhBMP2 and Submicron Particle of Biphasic Calcium Phosphate Ceramics with Through-Hole
title_fullStr Repair of Cranial Bone Defects Using rhBMP2 and Submicron Particle of Biphasic Calcium Phosphate Ceramics with Through-Hole
title_full_unstemmed Repair of Cranial Bone Defects Using rhBMP2 and Submicron Particle of Biphasic Calcium Phosphate Ceramics with Through-Hole
title_short Repair of Cranial Bone Defects Using rhBMP2 and Submicron Particle of Biphasic Calcium Phosphate Ceramics with Through-Hole
title_sort repair of cranial bone defects using rhbmp2 and submicron particle of biphasic calcium phosphate ceramics with through-hole
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600556/
https://www.ncbi.nlm.nih.gov/pubmed/26491693
http://dx.doi.org/10.1155/2015/926291
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