盐酸昂丹司琼分散片的研制及质量控制  

Preparation and Quality Control of Ondansetron Hydrochloride Dispersible Tablets

作　　者：刘祖雄[1] 王志朝[1] 王芳芳[1] 杜蓉[1] 汤韧[1] 龚志刚[1] 

机构地区：[1]广州军区武汉总医院,武汉市430070

出　　处：《中国药房》2002年第6期337-338,共2页China Pharmacy

摘　　要：目的 :研究盐酸昂丹司琼分散片的制备方法和质量控制。方法 :采用紫外分光光度法测定主药昂丹司琼的含量。结果 :线性范围为4 0～16 5μg/ml,平均回收率为99 97 % ,RSD为0 35 %。结论 :该制剂制备工艺简单 ,质量可控。OBJECTIVE:To study the preparation process and quality standard of ondansetron hydrochloride dispersible tablets METHODS:The content of ondansetron in the dispersible tablets was determined by UV-spectrophotometry RESULTS:The linear range was 4 0～16 5μg/ml,the average recovery was 99 97% with RSD of 0 35% CONCLUSION:The preparation process of ondansetron hydrochloride dispersible tablets is simple and the quality of dispersible tablets is controllable

关 键 词：盐酸昂丹司琼 分散片 制备 质量控制 

分 类 号：R975.4[医药卫生—药品]