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通过从生物功能化皮质同种异体移植物中联合递送 VEGF 和 BMP-2 实现大规模节段性骨缺损愈合。

Large scale segmental bone defect healing through the combined delivery of VEGF and BMP-2 from biofunctionalized cortical allografts.

机构信息

Department of Materials Science and Engineering, University of Connecticut, Storrs, Connecticut.

Institute for Regenerative Engineering, UConn Health, Farmington, Connecticut.

出版信息

J Biomed Mater Res B Appl Biomater. 2019 May;107(4):1002-1010. doi: 10.1002/jbm.b.34193. Epub 2018 Oct 8.

Abstract

Large scale cortical allografts suffer from poor incorporation and healing and often end in graft failure 5-10 years after implantation. To reduce these failures we have developed a growth-factor loaded cortical allograft capable of delivering one or two factors with a degree of temporal control and precision that permits the early release of one growth factor followed by the later and more sustained release of the other. We have loaded vascular endothelial growth factor (VEGF) and bone morphogenetic protein-2 (BMP-2), both critical components of bone formation and repair, onto cortical long bone allografts such that the VEGF is released first and followed shortly by BMP-2. Coated and factor-loaded allografts were placed into a critical sized rat femoral segmental defect and allowed to heal for either 4 or 8 weeks. Healing at each time point was compared to allografts loaded with only BMP-2 and allografts containing no growth factors. Results indicate statistically significant increases in new bone formation from 4 to 8 weeks around allografts loaded with both VEGF and BMP-2 over allografts with no growth factor, suggesting that factor-loaded polymer-coated allografts delivering multiple factors with temporal precision may provide a new off-the-shelf tool to the orthopedic surgeon for management of large-scale orthopedic bone defects. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B: 1002-1010, 2019.

摘要

大规模皮质同种异体移植物的整合和愈合效果较差,在植入后 5-10 年内往往会导致移植物失败。为了减少这些失败,我们开发了一种负载生长因子的皮质同种异体移植物,能够以一定的时间控制和精度递送一种或两种因子,从而允许早期释放一种生长因子,随后释放另一种生长因子。我们已经将血管内皮生长因子(VEGF)和骨形态发生蛋白-2(BMP-2)加载到皮质长骨同种异体移植物上,这两种因子都是骨形成和修复的关键组成部分,使得 VEGF 首先被释放,随后不久 BMP-2 被释放。涂覆有因子的同种异体移植物被放置在大鼠股骨节段性缺损的临界大小部位,并允许其愈合 4 或 8 周。在每个时间点比较了同时加载 VEGF 和 BMP-2 的同种异体移植物与仅加载 BMP-2 的同种异体移植物和不含生长因子的同种异体移植物的愈合情况。结果表明,与不含生长因子的同种异体移植物相比,同时加载 VEGF 和 BMP-2 的同种异体移植物在 4 至 8 周时新骨形成有统计学意义的增加,这表明具有时间精度的负载因子聚合物涂层同种异体移植物递送多种因子可能为骨科医生提供一种新的现成工具,用于管理大规模骨科骨缺损。©2018 年 Wiley 期刊,公司。J 生物医学材料研究部分 B:应用生物材料 107B:1002-1010,2019 年。

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