三维间充质干细胞负载淫羊藿苷缓释骨再生支架。

Yanbing Liu, Yan Fang
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引用次数: 1

摘要

背景/目的:采用同轴静电纺丝和生物静电喷涂的方法制备了载ICA的玉米蛋白/PLGA纳米纤维膜。材料与方法:采用扫描电镜(SEM)和透射电镜(TEM)对纤维膜的表面形貌和微观结构进行了表征。紫外分光光度法检测药物释放。采用LIVE/DEAD活力/细胞毒性试剂盒和荧光染色检测细胞形态和活性。采用碱性磷酸酶和钙矿化沉积法评价支架的骨诱导活性。采用动态力学分析确定制备的支架的杨氏模量、最大载荷和最大伸长率。Western blot检测载药支架诱导MSCs中相关蛋白的表达。结果:制备的载药支架具有良好的力学性能和稳定性。扫描电镜显示支架中有相当数量的间充质干细胞分散。MSCs分布均匀,能在纤维间均匀生长,并沿纤维有序排列。ICA的持续释放通过Runx2、OPN和OCN途径使细胞负载支架具有更高的ALP活性和ECM矿物沉积。结论:ICA的各向同性缓释使载细胞支架具有快速的骨再生能力,可为载细胞间充质干细胞提供良好的成骨环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Three-dimensional mesenchymal stem cell laden scaffold of icariin sustained-release for bone regeneration.

Three-dimensional mesenchymal stem cell laden scaffold of icariin sustained-release for bone regeneration.

Three-dimensional mesenchymal stem cell laden scaffold of icariin sustained-release for bone regeneration.

Three-dimensional mesenchymal stem cell laden scaffold of icariin sustained-release for bone regeneration.

Background/aim: Icariin (ICA)-loaded zein/PLGA nanofiber membrane combined with MSCs was prepared by coaxial electrospinning and bioelectrospraying.

Materials and methods: SEM and TEM were used to evaluate the surface morphology and microstructure of the fiber membrane. Ultraviolet spectrophotometry was used to detect drug release. A LIVE/DEAD Viability/Cytotoxicity Kit and fluorescence staining were used to detect cell morphology and activity. Alkaline phosphatase and calcium mineralization deposition were used to evaluate the osteoinductive activity of the scaffold. Dynamic mechanical analysis was used to determine the Young's modulus, maximum load, and maximum elongation of the prepared scaffold. Western blot was used to detect the related protein expression in MSCs induced by drug-loaded scaffolds.

Results: Good mechanical properties and stability were observed in the prepared drug-loaded scaffolds. SEM showed that there were a considerable number of MSCs dispersed in the scaffold. MSCs were evenly distributed, could grow evenly between fibers, and were arranged orderly along the fibers. Sustained release of ICA confers cell laden scaffold higher ALP activity and ECM mineral deposition through Runx2, OPN and OCN pathways.

Conclusion: Isotropic sustained release of ICA grant cell laden scaffolds rapid bone regeneration compacity which can provide a good osteogenic environment for loaded MSCs.

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