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作 者:关皎[1] 朱鹤云[1] 郝乘仪[1] 郭淑英[1] 冯波[1] GUAN Jiao ZHU Heyun HAO Chengyi GUO Shuying FENG Bo(College of Pharmacy, Jilin Medical University, Changchun 132013 Jilin, China)
出 处:《中药新药与临床药理》2017年第1期81-84,共4页Traditional Chinese Drug Research and Clinical Pharmacology
基 金:吉林省卫生厅科研课题(2013Z008)
摘 要:目的采用超快速液相色谱(UFLC)法同时测定龙胆中龙胆苦苷、獐芽菜苦苷和獐芽菜苷的含量。方法采用Shim-Pack XR-ODS柱(75 mm×3.0 mm,2.2μm),流动相为甲醇-0.1%磷酸水溶液(梯度洗脱),检测波长为240 nm,流速为0.5 m L·min^(-1),柱温为40℃。结果龙胆苦苷、獐芽菜苦苷和獐芽菜苷进样量分别在1.0~20μg(r=0.9998)、1.0~20μg(r=0.9995)、0.12~2.4μg(r=0.9996)范围内与峰面积呈良好的线性关系,平均加样回收率分别为97.3%、99.3%和98.3%(n=3),RSD均小于1.0%。结论 UFLC法简便、快速、准确、重现性好,可用于龙胆药材中环烯醚萜苷类成分的质量控制研究。Objective To develop an ultra-fast liquid chromatography(UFLC)method for simultaneous determination of gentiopicroside,swertiamarin and sweroside in Radix Gentianae. Methods Chromatographic separation was carried out on a Shim-Pack XR-ODS column(75 mm×3.0 mm,2.2 μm)with a mobile phase consisting of acetonitrile and water(containing 0.1 % phosphoric acid)by gradient elution at a flow rate of 0.5 m L·min-1. The detecting wavelength was set at 240 nm and the column temperature was maintained at 40 ℃. Results The calibration curves of gentiopicroside,swertiamarin and sweroside showed good linear relationship in the range of 1.0-20 μg(r=0.9998),1.0-20 μg(r=0.9995)and 0.12-2.4 μg(r=0.9996)respectively,and the average recovery(n=9)of three components was 97.3 %, 99.3 % and 98.3 % respectively, and the relative standard deviation(RSD) was less than 1.0 %.Conclusion The developed UFLC method is simple, rapid, accurate and repeatable, which is suitable for the quality control of gentiopicroside,swertiamarin and sweroside in Radix Gentianae.
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