以ZnO微球为模板,利用层层自组装的方法制备了壁材为鱼精蛋白(PRM)和硫酸葡聚糖(DXS)的生物可降解聚电解质胶囊.ZnO微球呈良好的单分散性,具有5nm以上的中孔,装载荧光素后生成荧光微球.在ZnO微球外交替吸附鱼精蛋白和硫酸葡聚糖,制得核-壳型ZnO/(DXS/PRM)。复合微球;采用稀HAC溶液去除ZnO模板后,可生成(DXS/PRM)8胶囊.以水溶性多柔米星药物分子作为目标物,研究了该胶囊的载药和释放行为.结果显示,该(DXS/PRM)8胶囊对多柔米星药物分子具有明显的缓释性.
Ultrathin polyelectrolyte capsules were produced by layer-by-layer assembling of biodegradable polyelectrolytes, dextran sulfate (DXS) and protamine (PRM), on ZnO microspheres followed by the cores decomposition with dilute HAC solution. ZnO microspheres were well mono-dispersed and had around 5 nm intermediate size pores, which could be used as fluorescein delivery. PRM and DXS formed regular growing stable multilayers on ZnO microspheres, thus formed ZnO/(DXS/PRM)8 core-shell microspheres. After removal of ZnO template, (DXS/PRM)8 capsules were fabricated. The loaded drug amount and controlled release behavior of hollow capsules were examined in the sample of dexorubicin hydrochloride (DOX). The result shows that (DXS/PRM)8 demonstates obvious controlled release of DOX drug.