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机构地区:[1]宁波市药品检验所,浙江宁波315048 [2]浙江医药高等专科学校
出 处:《中国药师》2014年第8期1316-1318,共3页China Pharmacist
摘 要:目的:建立高效液相色谱法测定布洛伪麻缓释片释放量的方法.方法:色谱柱为迪马C18(250 mm×4.6 mm,5μm),流动相为甲醇.三乙胺-0.04 mol·L-1磷酸二氢钠溶液(60:0.02:40),流速为1.0 ml·min-1,检测波长为215 nm,柱温为35℃,进样量为20μl.结果:布洛芬的线性范围为40~2 000 μg·ml-1(r=1.000 0),平均加样回收率为99.2%,RSD=0.8%(n=9),最低定量浓度为0.04μg· ml-1;盐酸伪麻黄碱的线性范围为6~300 μg· ml-1(r=1.000 0),平均加样回收率为98.5%,RSD =0.6% (n =9),最低定量浓度为0.06μg·ml-1.结论:该方法简便快速、准确灵敏,可用于布洛伪麻缓释片释放量的测定.Objective: To establish a method for the dissolution determination of ibuprofen and pseudoephedrine hydrochloride sus- tained-release tablets by HPLC. Methods: HPLC was adopted using a DIKMA C18 (250 mm × 4.6 mm,5 μm)column, the mobile phase consisted of methanol, triethylamine and 0.04 mol · L- 1 sodium dihydrogen phosphate solution (60: 0.02: 40) at the flow rate of 1.0 ml · min-1. The detection wavelength was 215nm. The column temperature was at 35℃ and the injection volume was 20 μl. Re- suits: A good linear correlation of ibuprofen was obtained within the range of 40-2 000 μg · ml - 1 ( r = 1. 000 0), the average recovery was 99.2% with RSD of 0.8% ( n = 9 ), and the limit of quantification was 0.04 μg · ml -1 The linear range of pseudoephedrine hydrochloride was 6-300 μg ·ml-1 ( r = 1. 000 0), the average recovery was 98.5% with RSD of 0.6% ( n = 9), and the limit of quantification was 0.06μg · ml-1. Conclusion: The method is rapid, simple, sensitive and accurate. It can be used to determine the released amount of ibuprofen and pseudoephedrine hydrochloride sustained-release tablets.
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