以牛血清白蛋白微泡为成孔剂制备可降解支架的新方法

A. Nair, Jian Yang, Liping Tang
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引用次数: 5

摘要

生物可降解支架在当代医学组织替代和再生中发挥着关键作用。许多可降解支架的制造技术已经被开发出来。然而,由于材料的疏水性和/或缺乏生物相容性蛋白涂层,这些支架经常阻碍细胞的生长。为了克服这些普遍存在的问题,本研究提出了利用蛋白质微泡作为多孔介质和药物/蛋白质载体来制备多孔性良好的聚合物支架的概念。在氮气的存在下,牛血清白蛋白超声产生白蛋白气泡。然后采用热诱导相分离法制备PLGA支架,并将蛋白微泡掺入成孔。扫描电镜和冷冻切片显示支架存在开放的相互连接的孔,大小约为100至150妈妈,适合细胞迁移到支架中。这种新技术有两个明显的优点。首先,微泡是由生物材料制成的,它可以在整个支架的孔上提供生物相容的蛋白质涂层。其次,与传统方法相比,我们的新型支架除了具有更大孔隙外,还具有将趋化因子和药物输送到聚合物基质中的输送机制的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel Preparation of Degradable Scaffolds Using BSA Microbubbles as Porogen
Biodegradable scaffolds play a key role in contemporary medicine for tissue replacement as well as regeneration. Many degradable scaffold fabrication techniques have been developed. However, these scaffolds often hamper the growth of cells due to material hydrophobicity and/or lack of biocompatible protein coating. To overcome the common problems, in this study, the use of protein microbubbles as a porogen and drug/protein carrier to produce polymeric scaffolds with good porosity was conceptualized. Albumin bubbles were produced by sonicating bovine serum albumin in the presence of nitrogen gas. PLGA scaffolds were then prepared by thermally induced phase separation with the incorporation of protein microbubbles as porogens. SEM and cryosectioning of scaffold revealed the presence of open interconnected pores measuring around 100 to 150 mum size, which is suitable for cell migration into scaffold. This novel technique provides two distinct advantages. First, microbubbles are made of biological materials which can provide biocompatible protein coating on the pores throughout the scaffold. Second, apart from having produced scaffolds with larger pores compared to conventional methods, our novel scaffold also has the potential to function as a delivery mechanism for delivering chemokines and drugs into the polymeric matrix.
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