摘要
目的:建立同时测定泽泻药材中23-乙酰泽泻醇C,泽泻醇A,24-乙酰泽泻醇A,泽泻醇G,泽泻醇B,23-乙酰泽泻醇B的UFLC含量分析方法.方法:采用Ultimate UFLC-AQ C18色谱柱(4.6 mm×100 mm,3μm),流动相乙腈(A)-水(B)进行梯度洗脱,流速0.3 mL· min-1,二极管阵列检测器的检测波长为208,245 nm,柱温30℃.结果:23-乙酰泽泻醇C,泽泻醇A,24-乙酰泽泻醇A,泽泻醇G,泽泻醇B,23-乙酰泽泻醇B6个成分的线性范围分别为0.179 0~17.88(r=0.999 8),0.500 0 ~100.0(r =0.999 7),0.216 0~25.20 (r=0.999 6),0.295 0~12.45 (r=1.000),0.653 0~65.33(r=0.999 6),0.393 0 ~ 78.32(r=0.999 8)mg·L-1;平均加样回收率分别为97.95%,96.70%,97.65%,96.01%,99.73%,100.3%.结论:建立的UFLC方法操作简便、快速、结果准确,适用于泽泻药材的质量控制.
Objective: To establish an ultra fast liquid chromatography (UFLC) method for simuhaneous determination of alisol C 23-acetate, alisol A, alisol A 24-acetate, alisol G, alisol B and alisol B 23- acetate in the Alismatis Rhizoma. Method: The seperation was performed on an Ultimate UFLC-AQ C18 column (2. 1 mm ×100 mm,3μ) using gradient elution with the mobile phase consisting of acetonitrile and water at a flow rate of 0.3 mL·min-1. The column temperature was maintained at 30 ℃ , and the DAD detection wavelengths were set at 208 nm and 245 nm. Result: The linear range of alisol C 23-acetate, alisol A, alisol A 24-acetate, alisol G, alisol B and alisol B 23-acetate were 0. 179 0-17. 88 (r =0. 999 8), 0. 500 0-100. 0 (r =0. 999 7), 0. 216 0- 25.20 (r=0.999 6), 0.295 0-12.45 (r=1.000), 0.653 0-65.33 (r =0.999 6), 0.393 0-78.32 mg·L-1 (r =0. 999 8) , respectively. The average recoveries were 97.95% , 96.70% , 97.65% , 96.01% , 99.73% , 100.30%. Conclusion: The results indicated that the developed method could be considered to be a simple, rapid and accurate method for the quality control of Alismatis Rhizoma.
出处
《中国实验方剂学杂志》
CAS
CSCD
北大核心
2015年第1期64-68,共5页
Chinese Journal of Experimental Traditional Medical Formulae
基金
国家自然科学基金项目(U1205022)
国家"十二五"科技支撑计划项目(2011BAI01B06)
福建省自然科学基金项目(2014J01352)
福建省卫生厅青年科研课题(2013-2-55)
福建中医药大学校管课题(X2012023)