Bhardwaj Peeyush, Chaurasia Himanshu, Chaurasia Deepti, Prajapati Sunil K, Singh Shobhna
Adarsh Vijendra Institute of Pharmaceutical Sciences, Gangoh, Saharanpur (U.P.), India.
Acta Pol Pharm. 2010 May-Jun;67(3):291-8.
Objective of present study involves preparation and evaluation of floating microballoons of indometacin as a model drug, to increase its residence time in the stomach without contact with the mucosa. The microballoons were prepared by the emulsion solvent diffusion technique using different ratio of acrylic polymers (Eudragit RS100 and Eudragit S 100) as carriers. The yield of microballoons was up to 91.02 +/- 1.65%. Microballoons showed passable flow properties. On the basis of optical microscopy, particle size range was found to be ranging from 130.90 +/- 12.10 to 170.58 +/- 17.50 microm. Scanning electron microscopy (SEM) confirmed their spherical size, perforated smooth surface and a hollow cavity in them. Microballoons exhibited floating properties for more than 10 h. In vitro drug studies were performed in 0.1 M HCI with 0.1% SLS and phosphate buffer (pH 6.2). Different drug release kinetics models were applied for selected batches.
本研究的目的是制备并评估作为模型药物的吲哚美辛漂浮微球,以增加其在胃中的停留时间而不与黏膜接触。使用不同比例的丙烯酸聚合物(Eudragit RS100和Eudragit S 100)作为载体,通过乳液溶剂扩散技术制备微球。微球的产率高达91.02 +/- 1.65%。微球表现出良好的流动性。基于光学显微镜,发现粒径范围为130.90 +/- 12.10至170.58 +/- 17.50微米。扫描电子显微镜(SEM)证实了它们的球形尺寸、穿孔的光滑表面以及内部的中空腔。微球表现出超过10小时的漂浮性能。在含有0.1%十二烷基硫酸钠(SLS)的0.1 M盐酸和磷酸盐缓冲液(pH 6.2)中进行体外药物研究。对选定批次应用了不同的药物释放动力学模型。