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机构地区:[1]广州市药品检验所,广州510160 [2]广州白云山光华制药股份有限公司,广州510285
出 处:《中国药品标准》2008年第5期354-356,共3页Drug Standards of China
摘 要:目的:建立HPLC法测定茶碱麻黄碱片中茶碱与盐酸麻黄碱的含量。方法:采用Diamonsil C18色谱柱,以甲醇-0.005mol·L^-1磷酸二氢钾溶液(含0.3%三乙胺,用磷酸调节pH值至3.0)(20:80)为流动相,流速为1.3mL·min^-1,检测波长210nm。结果:所选流动相适用范围较广,耐用性好,样品中两种成分分离度大。盐酸麻黄碱与茶碱分别在进样量在0.30—0.90μg(r=0.9997)和1.42~4.24μg(r=0.9993)范围线性关系良好,回收率分别为99.8%和100.0%(RSD分别为1.0%和0.8%)。结论:本法简便、准确、精密度高,可有效地控制茶碱麻黄碱片中双组分的含量。Objective:To develop an HPLC method to determine two components Theophylline and Ephedrine Hydrochloride in Chajian Mahuangjian Tablets. Method: Diamonsil C18 column was used. The mobile phase was consisted of methanol -0. 005 mol·L^-1 potassium dihydrogen phosphate solution(consisting 0. 3% triethylamine, adjust the pH value to 3.0 with phosphoric acid) (20: 80), at a flow rate of 1.3 mL · min^-1. The column temperature was 40% and the UV wavelength was 210 nm. Results: The mobile phase was widely applied and suitable to separate two components. A better linearity and good correlation coefficient were obtained: Ephedrine Hydrochloride was 0.30 - 0.90 μg ( r = 0. 999 7 ) ; Theophylline was 1.42- 4.24 μg ( r = 0. 999 3 ). The recovery were 99. 8% (RSD = 1.0% ) and 100.0% (RSD = 0. 8% ), respectively. Conclusions: The method is convenient, accurate, sensitive and suitable for quality control of the tablets.
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