摘要
目的:建立HPLC法测定参芪五味子片中的毛蕊异黄酮葡萄糖苷、五味子酯甲和五味子甲素含量的方法。方法:采用色谱柱:Agilent ZORBAX SBC18(250 mm×4.6 mm,5μm);以乙腈-0.1%磷酸水溶液为流动相进行梯度洗脱;流速:1.0 m L·min-1;检测波长:267 nm;柱温:28℃。结果:毛蕊异黄酮葡萄糖苷的进样量在0.11~2.75μg范围内(r=0.999 1)、五味子酯甲的进样量在1.05~26.25μg范围内(r=0.999 5)、五味子甲素的进样量在1.06~26.50μg范围内(r=0.999 4)线性关系良好,毛蕊异黄酮葡萄糖苷、五味子酯甲和五味子甲素的平均回收率分别为99.79%(RSD=1.43%,n=6)、99.37%(RSD=1.59%,n=6)和100.40%(RSD=2.11%,n=6)。结论:本方法简便快捷,重现性好,结果准确,适用于参芪五味子片的含量测定。
Objective: To establish a method for the determination of calycosin-7-glucoside,schisantherin and deoxyschizandrin in Shenqi Wuweizi Tablets. Methods: The separation was performed on a Agilent ZORBAX SBC18 column( 250 mm × 4. 6 mm,5 μm) with acetonitrile-0. 1% phosphoric acid solution as mobile phase with gradient elution at the flow rate was 1. 0 m L·min-1. The detection wavelength was set at 267 nm and the column temperature was 28 ℃.Results: The linear range of calycosin-7-glucoside,schisantherin and deoxyschizandrin was 0. 11-2. 75 μg( r = 0. 9991),1. 05-26. 25 μg( r = 0. 999 5) and 1. 06-26. 50 μg( r = 0. 999 4). The average recovery rates were 99. 79%( RSD= 1. 43%,n = 6),99. 37%( RSD = 1. 59%,n = 6) and 100. 40%( RSD = 2. 11%,n = 6),respectively. Conclusion: The established HPLC method is proved to be convenient,reproducible,precise and suitable for the content determination of Shenqi Wuweizi Tablets.
出处
《中华中医药学刊》
CAS
北大核心
2016年第8期1871-1873,共3页
Chinese Archives of Traditional Chinese Medicine
基金
中国博士后科学基金面上项目(2015M570257)
辽宁省科技事业公益研究基金项目(2014001021)