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作 者:谭生建 狄海涛 卢嘉琪[1,2] 付秀娟 常良才[1,2]
机构地区:[1]国防科工委药检所 [2]中国人民解放军第二炮兵药检所
出 处:《药物分析杂志》1999年第3期177-178,共2页Chinese Journal of Pharmaceutical Analysis
摘 要:目的:建立反相高效液相色谱测定清眩丸中欧前胡素含量的方法。方法:采用乙醇做溶剂,水浴加热回流提取。LUNA-C18色谱柱分离测定,流动相为乙腈-水(53∶47),流速1mL·min-1,检测波长300nm。结果:欧前胡素与其相邻峰的分离度是15,理论板数按欧前胡素峰计算是16155,欧前胡素对照品线性范围是1462~4875μg·mL-1,加样平均回收率980%。结论:用本文方法测定清眩丸中欧前胡素的含量,操作简便,结果准确。Objective: A reversed phase method was developed for the determination of imperatorin in Qingxuan Wan. Method: Sample was refluxed with ethanol in a water bath . Chromatographic conditions included a LUNA C18. column,mobile phase, acetonitrile-water (5347), flow rate 1 mLmin-1; SPD6AV uv-vis spectrophotometric detector at wavelength of 300 nm . Results: The number of theoretical plates calculated by imperatorin peak was 16155, R=15. The standard curve was linear in the concentration range of 14624875 gmL-1.The average recovery was 980%. Conclusion: The method was sensitive, rapid and accurate.
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