Fabrication of Rosuvastatin-Incorporated Polycaprolactone -Gelatin Scaffold for Bone Repair: A Preliminary In Vitro Study.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Maliheh Gharibshahian, Morteza Alizadeh, Mohammad Kamalabadi Farahani, Majid Salehi
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引用次数: 0

Abstract

Objective: Rosuvastatin (RSV) is a hydrophilic, effective statin with a long half-life that stimulates bone regeneration. The present study aims to develop a new scaffold and controlled release system for RSV with favourable properties for bone tissue engineering (BTE).

Materials and methods: In this experimental study, high porous polycaprolactone (PCL)-gelatin scaffolds that contained different concentrations of RSV (0 mg/10 ml, 0.1 mg/10 ml, 0.5 mg/10 ml, 2.5 mg/10 ml, 12.5 mg/10 ml, and 62.5 mg/10 ml) were fabricated by the thermally-induced phase separation (TIPS) method. Mechanical and biological properties of the scaffolds were evaluated by Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), compressive strength, porosity, MTT, alkaline phosphatase (ALP) activity, water contact angle, degradation rate, pH alteration, blood clotting index (BCI), and hemocompatibility.

Results: SEM analysis confirmed that the porous structure of the scaffolds contained interconnected pores. FTIR results showed that the RSV structure was maintained during the scaffold's fabrication. RSV (up to 62.5 mg/10 ml) increased compressive strength (16.342 ± 1.79 MPa), wettability (70.2), and degradation rate of the scaffolds. Scaffolds that contained 2.5 mg/10 ml RSV had the best effect on the human umbilical cord mesenchymal stem cell (HUC-MSCs) survival, hemocompatibility, and BCI. As a sustained release system, only 31.68 ± 0.1% of RSV was released from the PCL-Gelatin-2.5 mg/10 ml RSV scaffold over 30 days. In addition, the results of ALP activity showed that RSV increased the osteogenic differentiation potential of the scaffolds.

Conclusion: PCL-Gelatin-2.5 mg/10 ml RSV scaffolds have favorable mechanical, physical, and osteogenic properties for bone tissue and provide a favorable release system for RSV. They can mentioned as a a promising strategy for bone regeneration that should be further assessed in animals and clinical studies.

用于骨修复的瑞舒伐他汀掺入聚己内酯-明胶支架的制作:体外初步研究
目的:瑞舒伐他汀(RSV)是一种半衰期长的亲水性高效他汀类药物,可刺激骨再生。本研究旨在为 RSV 开发一种新的支架和控释系统,该系统具有有利于骨组织工程(BTE)的特性:在本实验研究中,采用热诱导相分离(TIPS)方法制备了含有不同浓度 RSV(0 毫克/10 毫升、0.1 毫克/10 毫升、0.5 毫克/10 毫升、2.5 毫克/10 毫升、12.5 毫克/10 毫升和 62.5 毫克/10 毫升)的高孔聚己内酯(PCL)-明胶支架。通过傅立叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、抗压强度、孔隙率、MTT、碱性磷酸酶(ALP)活性、水接触角、降解率、pH值变化、血液凝固指数(BCI)和血液相容性对支架的机械和生物特性进行了评估:扫描电子显微镜分析证实,支架的多孔结构包含相互连接的孔。傅立叶变换红外光谱(FTIR)结果表明,支架制造过程中保持了 RSV 结构。RSV(高达 62.5 毫克/10 毫升)提高了支架的抗压强度(16.342 ± 1.79 兆帕)、润湿性(70.2)和降解率。含有 2.5 毫克/10 毫升 RSV 的支架对人脐带间充质干细胞(HUC-MSCs)的存活、血液相容性和 BCI 效果最好。作为一种缓释系统,30 天内只有 31.68 ± 0.1% 的 RSV 从 PCL-Gelatin-2.5 mg/10 ml RSV 支架中释放出来。此外,ALP活性结果表明,RSV提高了支架的成骨分化潜力:PCL-Gelatin-2.5 mg/10 ml RSV 支架对骨组织具有良好的机械、物理和成骨特性,并为 RSV 提供了良好的释放系统。结论:PCL-明胶-2.5 毫克/10 毫升 RSV 支架对骨组织具有良好的机械、物理和成骨特性,并为 RSV 提供了良好的释放系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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