Department of Pharmaceutical Sciences, Mahatma Gandhi University, Cheruvandoor Campus, Ettumanoor-686 631, Kerala, India.
Colloids Surf B Biointerfaces. 2011 Apr 1;83(2):277-83. doi: 10.1016/j.colsurfb.2010.11.033. Epub 2010 Dec 1.
In the present work, chitosan microspheres with a mean diameter between 6.32 μm and 9.44 μm, were produced by emulsion cross-linking of chitosan, and tested for chronotherapy of chronic stable angina. Aiming at developing a suitable colon specific strategy, diltiazem hydrochloride (DTZ) was encapsulated in the microspheres, following Eudragit S-100 coating by solvent evaporation technique, exploiting the advantages of microbiological properties of chitosan and pH dependent solubility of Eudragit S-100. Different microsphere formulations were prepared varying the ratio DTZ:chitosan (1:2 to 1:10), stirring speed (1000-2000 rpm), and the concentration of emulsifier Span 80 (0.5-1.5% (w/v)). The effect of these variables on the particle size and encapsulation parameters (production yield (PY), loading capacity (LC), encapsulation efficiency (EE)) was evaluated to develop an optimized formulation. In vitro release study of non-coated chitosan microspheres in simulated gastrointestinal (GI) fluid exhibited a burst release pattern in the first hour, whereas Eudragit S-100 coating allowed producing systems of controlled release diffusion fitting to the Higuchi model, and thus suitable for colon-specific drug delivery. DSC analysis indicated that DTZ was dispersed within the microspheres matrix. Scanning electron microscopy revealed that the microspheres were spherical and had a smooth surface. Chitosan biodegradability was proven by the enhanced release rate of DTZ in presence of rat caecal contents.
在本工作中,通过壳聚糖的乳化交联制备了平均直径在 6.32μm 和 9.44μm 之间的壳聚糖微球,并对其进行了慢性稳定性心绞痛的时间治疗测试。为了开发合适的结肠特异性策略,将盐酸地尔硫卓(DTZ)包封在微球中,随后通过溶剂蒸发技术用 Eudragit S-100 进行包衣,利用壳聚糖的微生物学性质和 Eudragit S-100 的 pH 依赖性溶解度的优势。通过改变 DTZ:壳聚糖的比例(1:2 至 1:10)、搅拌速度(1000-2000rpm)和乳化剂 Span 80 的浓度(0.5-1.5%(w/v)),制备了不同的微球配方。评估这些变量对粒径和包封参数(产率(PY)、载药量(LC)、包封效率(EE))的影响,以开发优化的配方。在模拟胃肠道(GI)液中的非包衣壳聚糖微球的体外释放研究中,在最初的 1 小时内呈现出爆发释放模式,而 Eudragit S-100 包衣允许产生符合 Higuchi 模型的控释扩散系统,从而适合结肠特异性药物传递。差示扫描量热法(DSC)分析表明,DTZ 分散在微球基质中。扫描电子显微镜显示微球呈球形,表面光滑。壳聚糖的生物降解性通过在大鼠盲肠内容物存在下 DTZ 的释放率提高得到证明。