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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Osteogenic effect of controlled released rhBMP-2 in 3D printed porous hydroxyapatite scaffold
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Osteogenic effect of controlled released rhBMP-2 in 3D printed porous hydroxyapatite scaffold

机译:受控释放的rhBMP-2在3D打印的多孔羟基磷灰石支架中的成骨作用

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摘要

Recently, 3D printing as effective technology has been highlighted in the biomedical field. Previously, a porous hydroxyapatite (HA) scaffold with the biocompatibility and osteoconductivity has been developed by this method. However, its osteoinductivity is limited. The main purpose of this study was to improve it by the introduction of recombinant human bone morphogenetic protein-2 (rhBMP-2). This scaffold was developed by coating rhBMP-2-delivery microspheres with collagen. These synthesized scaffolds were characterized by Scanning Electron Microscopy (SEM), a delivery test in vitro, cell culture, and the experiments in vivo by a Micro-computed tomography (mu CT) scan and histological evaluation of VanGieson staining. SEM results indicated the surface of scaffolds were more fit for the adhesion of hMSCs to coat collagen/rhBMP-2 microspheres. Biphasic release of rhBMP-2 could continue for more than 21 days, and keep its osteoinductivity to induce osteogenic differentiation of hMSCs in vitro. In addition, the experiments in vivo showed that the scaffold had a good bone regeneration capacity. These findings demonstrate that the HA/Collagen/Chitosan Microspheres system can simultaneously achieve localized long-term controlled release of rhBMP-2 and bone regeneration, which provides a promising route for improving the treatment of bone defects. (C) 2016 The Authors. Published by Elsevier B.V.
机译:近来,3D打印作为一种有效技术已在生物医学领域得到了强调。以前,已经通过这种方法开发了具有生物相容性和骨传导性的多孔羟基磷灰石(HA)支架。但是,其骨诱导能力是有限的。这项研究的主要目的是通过引入重组人骨形态发生蛋白2(rhBMP-2)对其进行改进。通过用胶原蛋白包被rhBMP-2-递送微球来开发该支架。这些合成的支架通过扫描电子显微镜(SEM),体外递送测试,细胞培养以及体内实验通过微计算机断层扫描(mu CT)扫描和VanGieson染色的组织学评估进行表征。 SEM结果表明支架表面更适合hMSCs粘附胶原/ rhBMP-2微球。 rhBMP-2的双相释放可能会持续21天以上,并保持其骨诱导能力,从而在体外诱导hMSC的成骨分化。另外,体内实验表明该支架具有良好的骨再生能力。这些发现表明,HA /胶原蛋白/壳聚糖微球系统可以同时实现rhBMP-2的局部长期控制释放和骨再生,这为改善骨缺损的治疗提供了有希望的途径。 (C)2016作者。由Elsevier B.V.发布

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