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机构地区:[1]广州白云山星群(药业)股份有限公司,广州510288
出 处:《中国实验方剂学杂志》2013年第24期75-77,共3页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家科技部重大新药创制项目(2011ZX09401-404-02)
摘 要:目的: 建立夏桑菊颗粒中迷迭香酸、异迷迭香酸苷2成分含量测定方法。方法: 采用HPLC同时测定夏桑菊颗粒中迷迭香酸、异迷迭香酸含量,Agilent Eclipse XDB-C18色谱柱(4.6 mm×250 mm,5 μm),流动相乙腈-0.1%磷酸梯度洗脱,流速1.0 mL·min-1,检测波长319 nm,柱温30℃。结果: 迷迭香酸、异迷迭香酸苷线性范围分别为0.036 4-0.364 μg(R2=0.999 8),0.004 98-0.049 8 μg(R2=0.999 7);迷迭香酸平均回收率为99.16%,RSD 1.32%,异迷迭香酸苷平均回收率为98.40%,RSD 0.78%(n=6)。结论: 该方法操作简单,可靠,重复性好,可用于控制夏桑菊颗粒质量控制。Objective: To develop a HPLC method for simultaneous determination of rosmarinic acid and salviaflaside in Xiasangju Granules. Method: An Agilent Eclipse XDB-C18 column (4.6 mm×250 mm, 5 μm) was applied with gradient elution using acetonitrile and 0.1% phosphoric acid as mobile phase, and the flow rate was 1.0 mL·min-1. The UV detector was set at 319 nm. Result: The linear range of rosmarinic acid was 0.036 4-0.364 μg, and the average recovery was 99.16%. The linear range of salviaflaside was 0.004 98-0.049 8 μg and the average recovery was 98.40%(n=6). Conclusion: The method is accurate and repeatable. It can be used for quality evaluation of Xiasangju Granules.
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