Department of Bioengineering, Faculty of Engineering, National University of Singapore, Singapore 117574, Singapore.
Biomacromolecules. 2012 Jul 9;13(7):2174-80. doi: 10.1021/bm3005879. Epub 2012 Jun 14.
Basic fibroblast growth factor (FGF2) is an important protein for cellular activity and highly vulnerable to environmental conditions. FGF2 protected by heparin and bovine serum albumin was loaded into the microcapsules by a coprecipitation-based layer-by-layer encapsulation method. Low cytotoxic and biodegradable polyelectrolytes dextran sulfate and poly-L-arginine were used for capsule shell assembly. The shell thickness-dependent encapsulation efficiency was measured by enzyme-linked immunosorbent assay. A maximum encapsulation efficiency of 42% could be achieved by microcapsules with a shell thickness of 14 layers. The effects of microcapsule concentration and shell thickness on cytotoxicity, FGF2 release kinetics, and L929 cell proliferation were evaluated in vitro. The advantage of using microcapsules as the carrier for FGF2 controlled release for enhancing L929 cell proliferation was analyzed.
碱性成纤维细胞生长因子(FGF2)是一种对细胞活动非常重要的蛋白质,并且极易受到环境条件的影响。肝素和牛血清白蛋白保护的 FGF2 采用基于共沉淀的层层包封方法载入微胶囊中。低细胞毒性和可生物降解的聚电解质硫酸葡聚糖和聚-L-精氨酸用于胶囊壳的组装。通过酶联免疫吸附试验测量了壳厚度依赖性的包封效率。壳厚度为 14 层的微胶囊可达到 42%的最大包封效率。体外评估了微胶囊浓度和壳厚度对细胞毒性、FGF2 释放动力学和 L929 细胞增殖的影响。分析了使用微胶囊作为 FGF2 控释载体以增强 L929 细胞增殖的优势。