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出 处:《中国药业》2006年第18期20-21,共2页China Pharmaceuticals
摘 要:目的建立用高效液相色谱法测定复方氨酚烷胺胶囊中对乙酰氨基酚、咖啡因、马来酸氯苯那敏含量的方法。方法采用ODSC18柱(150mm×4.6mm,5μm),以甲醇-0.05mol/L磷酸二氢钾-三乙胺(20∶80∶0.02)为流动相。结果对乙酰氨基酚、咖啡因、马来酸氯苯那敏浓度线性范围分别为101.272~911.448,6.356~57.204,0.804~7.236μg/mL,平均回收率分别为99.21%,100.14%,101.37%,RSD分别为0.25%,0.27%,0.60%(n=5)。结论该方法准确、简便、快速,适于复方氨酚烷胺胶囊的含量测定。Objective To develop a HPLC method for determination of paracetamol,caffeine and chlorphnamine maleate in compound paracetamol and amantadine hydrochloride capsules. Methods ODS C18 column was used and the mobile phase was methanol-0. 05 mol/L potassium dihydrogen phosphate-triacetamide (20:80:0. 02). Results The calibration curves for paracetamol,caffeine and chlorphnamine maleate were linear over the range of 101. 272 - 911. 448,6. 356 - 57. 204,0. 804 - 7. 236 μg/mL, respectively. The average recovery rates were 99.21% , 100. 14% , 101.37% with RSD were 0. 25% ,0. 27% and 0. 60% ( n = 5),respectively. Conclusion The method is accurate, rapid and simple,bing applicable for the assay of compound paracetamol and amantadine hydroehloride capsules.
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