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作 者:黄彩虹[1] 雷鹏[1] 甘莲莲[1] 黄义[1,2] 李新中[1]
机构地区:[1]中南大学湘雅医院药剂科,长沙410008 [2]中南大学药学院,长沙410013
出 处:《中南药学》2009年第6期408-410,共3页Central South Pharmacy
基 金:湖南省卫生厅中医药科技基金项目(编号:6304-78);长沙市科技局重点项目(编号:K0802115-31)
摘 要:目的建立高效液相色谱法测定地锦草中没食子酸的含量。方法DiamonsilC18色谱柱(4.6mm×250mm,5μm);流动相:甲醇-0.01%磷酸(10:90);检测波长:273nm柱温:30℃;流速:1mL·min^-1,进样量:5μL。结果没食子酸在0.0t82~0.1824μg线性关系良好,回归方程为Y=2969.4X-4.252,r=0.9999。平均加样回收率为98.36%,RSD为2.83%。结论本方法简便、快速、重复性好,可用于测定地锦草中没食子酸的含量。Objective To establish an HPLC method for the determination of gallic acid in Herba Euphorbia humifusac. Methods The chromatographic system consisted of a Diamonsil C18 column (4.6 mm ×250mm, 5 μm) and a mobile phase of MeOH-0.01%H3PO4 (10 : 90). The detection wavelength was 273 nm. The column temperature was 30 ℃ and the flow rate was 1 mL ·min^-1. Results A good linearity of gallic acid was in the range of 0. 018 2-0. 1824μg, the regression equation was Y= 2 969. 4 X--4. 252, and r was 0. 999 9. The average recovery was 98.36% and RSD was 2.83%. Conclusion The HPLC method is simple, rapid and accurate, which can be used for the determination of gallic acid in Herba Euphorbia humifusae.
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