Sui Weiping, Huang Liangliang, Wang Jun, Bo Qibing
School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, China.
Colloids Surf B Biointerfaces. 2008 Aug 1;65(1):69-73. doi: 10.1016/j.colsurfb.2008.02.022. Epub 2008 Mar 14.
The chitosan (CHS) chondroitin sulfate (CS) complex microcapsules were prepared by emulsion-chemical crosslink method, with the chitosan and chondroitin sulfate as the wall materials and the low molecular weight heparin (LMWH) as the core materials. The microcapsules were characterized by Fourier transform infrared (IR) spectrometry, scanning electron microscope (SEM), size distribution and thermal analysis. The in vitro drug release behavior of the microcapsules was studied by spectrophotometry. The SEM and size distribution showed that the microcapsules were in the spherical form mostly in the size range of 20-80 microm. The IR spectrum indicated that there were electrostatic interactions between chitosan and chondroitin sulfate, with the sulfate group and free carboxyl group reacted with the amino groups of chitosan. The DSC result showed that the wall materials could protect the core materials of the microcapsules. The results of the release kinetics experiments of the microcapsules showed that the drug released slightly faster in acid media than in alkali ones.
以壳聚糖(CHS)和硫酸软骨素(CS)为壁材、低分子肝素(LMWH)为芯材,采用乳化-化学交联法制备了壳聚糖-硫酸软骨素复合微胶囊。通过傅里叶变换红外(IR)光谱、扫描电子显微镜(SEM)、粒径分布和热分析对微胶囊进行了表征。采用分光光度法研究了微胶囊的体外药物释放行为。SEM和粒径分布表明,微胶囊大多呈球形,粒径范围为20-80微米。IR光谱表明壳聚糖与硫酸软骨素之间存在静电相互作用,硫酸根和游离羧基与壳聚糖的氨基发生了反应。DSC结果表明壁材可以保护微胶囊的芯材。微胶囊释放动力学实验结果表明,药物在酸性介质中的释放速度略快于碱性介质。