The multiparticulate formulation of sodium para aminosalicylate for oral administration was developed by extrusion spheronization technique. Microcrystalline cellulose was used as filler in concentration of 14.4% w/w. Pellets were coated with Eudragit L 30 D-55 using fluidized bed processor. Different weight gains of acrylic polymer were applied onto the pellets and evaluated for in vitro dissolution behavior in 0.1 N HCl for two hours and then media was changed to phosphate buffer pH 6.8. A 60% w/w coating level of Eudragit L30 D 55 has produced the most acceptable results against the gastric attack. 3% Seal coat of HPMC E5 was also applied in order to protect the drug from migration into the Eudragit coat and film coat was applied in order to prevent aggregation of pellets in the dissolution media. Morphological characteristics of developed pellets were also investigated by scanning electron microscopy and found to be smooth and spherical. Developed system was found to be suitable for the delivery of Sod PAS in to intestinal region.
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机译:通过挤出滚圆技术开发了口服对氨基水杨酸钠的多颗粒制剂。使用微晶纤维素作为填充剂,其浓度为14.4%w / w。使用流化床处理器将丸粒用Eudragit L 30 D-55包衣。将不同重量增加的丙烯酸聚合物施加到小球上,并评估其在0.1 N HCl中的体外溶解行为2小时,然后将介质更改为pH 6.8的磷酸盐缓冲液。 Eudragit L30 D 55的60%w / w涂层水平产生了最可接受的抗胃癌作用。为了防止药物迁移到Eudragit涂层中,还施加了3%的HPMC E5密封涂层,并施加了薄膜涂层以防止沉淀物在溶出介质中聚集。还通过扫描电子显微镜研究了所形成的丸粒的形态特征,发现其是光滑的和球形的。发现开发的系统适合将Sod PAS输送到肠道区域。
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