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负载辛伐他汀的聚乳酸-羟基乙酸共聚物微球的多孔壳聚糖/纳米羟基磷灰石复合支架用于骨修复

Porous Chitosan/Nano-Hydroxyapatite Composite Scaffolds Incorporating Simvastatin-Loaded PLGA Microspheres for Bone Repair.

作者信息

Li Yu, Zhang Zhanzhao, Zhang Zhiyong

出版信息

Cells Tissues Organs. 2018;205(1):20-31. doi: 10.1159/000485502. Epub 2018 Feb 1.

DOI:10.1159/000485502
PMID:29393155
Abstract

The combination of bone tissue scaffolds with osteogenic induction factors is an effective strategy to facilitate bone healing processes. Here, chitosan (CS)/nano-hydroxyapatite (HA) scaffolds containing simvastatin (SIM)-loaded PLGA microspheres were fabricated by combining a freeze-drying technique with a modified water-oil-water emulsion method. The CS/HA weight ratio of 1:2 was selected by analyzing the effect of HA content on the micro-architecture, mechanical strength, and biocompatibility of the scaffold. Drug release kinetics showed that the SIM encapsulated in the scaffold was released in a sustained manner for up to 30 days. In vitro bioactivity study in rat bone marrow-derived mesenchymal stem cells showed that the SIM-loaded scaffolds had a strong ability in accelerating cell proliferation and inducing osteogenic differentiation. Moreover, an in vivo experiment using a rat calvarial defect model also documented that the SIM-loaded scaffolds had a remarkable effect on bone-promoting regeneration. The results of this study suggest that the SIM-loaded CS/HA scaffold is feasible and effective in bone repair and thus may provide a promising route for the treatment of critical-sized bone defects.

摘要

骨组织支架与成骨诱导因子相结合是促进骨愈合过程的有效策略。在此,通过将冷冻干燥技术与改进的水包油包水乳液法相结合,制备了含有载辛伐他汀(SIM)的聚乳酸-羟基乙酸共聚物(PLGA)微球的壳聚糖(CS)/纳米羟基磷灰石(HA)支架。通过分析HA含量对支架微观结构、机械强度和生物相容性的影响,选择了CS/HA重量比为1:2。药物释放动力学表明,包裹在支架中的SIM持续释放长达30天。对大鼠骨髓间充质干细胞的体外生物活性研究表明,载SIM的支架具有很强的促进细胞增殖和诱导成骨分化的能力。此外,使用大鼠颅骨缺损模型的体内实验也证明,载SIM的支架对促进骨再生有显著效果。本研究结果表明,载SIM的CS/HA支架在骨修复中是可行且有效的,因此可能为治疗临界尺寸骨缺损提供一条有前景的途径。

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