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RhBMP-2 loaded 3D-printed mesoporous silica/calcium phosphate cement porous scaffolds with enhanced vascularization and osteogenesis properties

机译:装有RhBMP-2的3D打印的介孔二氧化硅/磷酸钙水泥多孔支架具有增强的血管形成和成骨特性

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摘要

A major limitation in the development of effective scaffolds for bone regeneration has been the limited vascularization of the regenerating tissue. Here, we propose the development of a novel calcium phosphate cement (CPC)-based scaffold combining the properties of mesoporous silica (MS) with recombinant human bone morphogenic protein-2 (rhBMP-2) to facilitate vascularization and osteogenesis. Specifically, the development of a custom MS/CPC paste allowed the three-dimensional (3D) printing of scaffolds with a defined macroporous structure and optimized silicon (Si) ions release profile to promote the ingrowth of vascular tissue at an early stage after implantation in support of tissue viability and osteogenesis. In addition, the scaffold microstructure allowed the prolonged release of rhBMP-2, which in turn significantly stimulated the osteogenesis of human bone marrow stromal cells in vitro and of bone regeneration in vivo as shown in a rabbit femur defect repair model. Thus, the combination MS/CPC/rhBMP-2 scaffolds might provide a solution to issues of tissue necrosis during the regeneration process and therefore might be able to be readily developed into a useful tool for bone repair in the clinic.
机译:开发有效的骨再生支架的主要限制是再生组织的血管生成受限。在这里,我们提出了一种新型的基于磷酸钙水泥(CPC)的支架的开发,该支架结合了介孔二氧化硅(MS)与重组人骨形态发生蛋白2(rhBMP-2)的特性来促进血管生成和成骨。具体而言,定制MS / CPC糊剂的开发可对具有定义的大孔结构和优化的硅(Si)离子释放曲线的支架进行三维(3D)打印,从而在植入后的早期促进血管组织向内生长。支持组织活力和成骨。另外,支架的微结构允许rhBMP-2的延长释放,这反过来显着刺激了体外人骨髓基质细胞的成骨作用和体内股骨再生的刺激,如兔股骨缺损修复模型所示。因此,组合的MS / CPC / rhBMP-2支架可以为再生过程中的组织坏死问题提供解决方案,因此可以很容易地发展成为临床上用于骨修复的有用工具。

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