...
首页> 外文期刊>The international journal of artificial organs >Development of a simvastatin loaded injectable porous scaffold in situ formed by phase inversion method for bone tissue regeneration
【24h】

Development of a simvastatin loaded injectable porous scaffold in situ formed by phase inversion method for bone tissue regeneration

机译:骨组织再生方法骨组织再生方法的原位开发辛伐他汀装载的可注射多孔支架

获取原文
获取原文并翻译 | 示例
           

摘要

Introduction: The use of injectable scaffolds as a minimally invasive method is a good choice in tissue engineering applications. A critical parameter for the tissue engineering scaffolds is a suitable morphology with interconnected pores. We present the development of a simvastatin loaded scaffold that forms in situ and provides the porous structure with interconnected pores. Methods: The formulation of these scaffolds includes a polymeric solution of poly lactic-co-glycolic acid (25 wt%) in N-methyl-2-pyrrolidone containing 6 wt% deionized water and porogen (mannitol, four times the weight of the polymer). We have grafted simvastatin to poly lactic-co-glycolic acid by the esterification reactions. Simvastatin or simvastatin-grafted poly lactic-co-glycolic acid in different levels was added to polymer solution and finally the solution was injected into phosphate buffered saline. The simvastatin-grafted poly lactic-co-glycolic acid was characterized by attenuated total reflection Fourier-transform infra-red and H-1-nuclear magnetic resonance spectroscopy. The morphology, porosity, and biocompatibility of the scaffolds were evaluated. The in vitro simvastatin release from the various formulations was studied. Osteogenic differentiation of the adipose-derived stem cells was investigated using alkaline phosphatase activity assay and cell mineralization was evaluated using Alizarin red staining. Results: The morphology results showed the resultant scaffold was porous with the interconnected pores. The scaffolds presented 91% porosity. Non-toxic doses of simvastatin in the scaffolds were determined by methyl-thiazolyl diphenyl-tetrazolium bromide assay. The released simvastatin from the scaffolds continues over 80 days. Alkaline phosphatase activity and Alizarin red results indicated that cell osteogenic differentiation is promoted. Conclusion: The results demonstrated that release of simvastatin from the injectable scaffolds can have positive effects on osteogenic differentiation of the adipose-derived stem cells.
机译:简介:使用可注射支架作为微创方法是组织工程应用的良好选择。组织工程支架的关键参数是具有相互连接的孔的合适形态。我们展示了一种辛伐他汀装载脚手架的发展,其原位形成并提供具有相互连接的孔的多孔结构。方法:这些支架的配方包括在含有6wt%去离子水和孔胶(甘露醇的甘氨酸的N-甲基-2-吡咯烷酮中的聚乳酸二乙醇酸(25wt%)的聚合物溶液(甘露醇,聚合物重量的四倍)。我们通过酯化反应嫁接辛伐他汀来聚合乳酸 - 共乙醇酸。将辛伐他汀或辛伐他汀接枝的聚乳酸 - 共乙醇酸在不同水平中加入聚合物溶液中,最后将溶液注入磷酸盐缓冲盐水中。通过减弱的全反射傅里叶变换红外线和H-1核磁共振谱来表征辛伐他汀接枝的聚乳酸共甘油酸。评价支架的形态,孔隙率和生物相容性。研究了各种配方中的体外辛伐他汀释放。研究了使用碱性磷酸酶活性测定来研究脂肪衍生的干细胞的成骨分化,并使用茜素红染色评价细胞矿化。结果:形态学结果显示所得支架与互连孔隙多孔。支架呈现出91%的孔隙率。通过甲基 - 噻唑基二苯基 - 四唑溴铵测定法测定支架中的无毒剂量的辛伐他汀。来自支架的释放的辛伐他汀在80天内继续。碱性磷酸酶活性和茜素红色结果表明,促进了细胞骨化分化。结论:结果表明,从可注射支架中释放辛伐他汀可以对脂肪衍生的干细胞的骨质发生分化具有积极影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号