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Micro-Nano Bioactive Glass Particles Incorporated Porous Scaffold for Promoting Osteogenesis and Angiogenesis in vitro

机译:微纳米生物活性玻璃颗粒掺入多孔支架在体外促进成骨和血管生成。

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摘要

Constructing the interconnected porous biomaterials scaffolds with osteogenesis and angiogenesis capacity is extremely important for efficient bone tissue engineering. Herein, we fabricated a bioactive micro-nano composite scaffolds with excellent in vitro osteogenesis and angiogenesis capacity, based on poly (lactic-co-glycolic acid) (PLGA) incorporated with micro-nano bioactive glass (MNBG). The results showed that the addition of MNBG enlarged the pore size, increased the compressive modulus (4 times improvement), enhanced the physiological stability and apatite-forming ability of porous PLGA scaffolds. The in vitro studies indicated that the PLGA-MNBG porous scaffold could enhance the mouse bone mesenchymal stem cells (mBMSCs) attachment, proliferation, and promote the expression of osteogenesis marker (ALP). Additionally, PLGA-MNBG could also support the attachment and proliferation of human umbilical vein endothelial cells (HUVECs), and significantly enhanced the expression of angiogenesis marker (CD31) of HUVECs. The as-prepared bioactive PLGA-MNBG nanocomposites scaffolds with good osteogenesis and angiogenesis probably have a promising application for bone tissue regeneration.
机译:具有骨生成和血管生成能力的互连多孔生物材料支架的构建对于有效的骨组织工程极为重要。在本文中,我们基于结合了微纳米生物活性玻璃(MNBG)的聚乳酸-乙醇酸(PLGA),制造了具有出色的体外成骨和血管生成能力的生物活性微纳米复合支架。结果表明,添加MNBG可以扩大孔径,提高压缩模量(提高4倍),增强多孔PLGA支架的生理稳定性和磷灰石形成能力。体外研究表明,PLGA-MNBG多孔支架可以增强小鼠骨髓间充质干细胞(mBMSCs)的附着,增殖并促进成骨标记(ALP)的表达。此外,PLGA-MNBG还可以支持人脐静脉内皮细胞(HUVEC)的附着和增殖,并显着增强HUVEC的血管生成标记(CD31)的表达。制备的具有良好成骨性和血管生成性的生物活性PLGA-MNBG纳米复合材料支架可能在骨组织再生中具有广阔的应用前景。

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