摘要
目的:运用安捷伦1260高效液相色谱仪,建立多波长切换技术,同时测定加味小柴胡胶囊中党参炔苷、甘草苷、黄芩苷、黄芩素含量的方法。方法:采用菲罗门ODS C18柱,以乙腈(流动相A)-0.1%磷酸水溶液为流动相体系,梯度洗脱(0~40分钟,乙腈20%~45%),流速1.0 m L/min,一般波长254 nm,检测波长在每个成分出峰的时间段内切换为该成分最大吸收波长。结果:甘草苷、党参炔苷、黄芩苷、黄芩素分别在0.05~0.75、0.042~0.63、0.80~12.0、0.04~0.60μg范围内线性关系良好。相关系数分别为0.9995、0.9992、0.9999和0.9997,平均加样回收率分别为100.31%、98.92%、101.06%、100.17%,RSD%分别为1.90、1.63、2.21、1.19。结论:本研究建立的方法稳定可靠,便于操作,可以解决党参炔苷因含量较低无法检测的问题。
Objective: To establish wavelength switching method for detecting the contents of lobetyolin, liquiritin, baicalin and baicalein contained in modified XiaoChaiHu capsules by using HPLC (Agilent 1260) simultaneously. Methods: HPLC separation was performed on Phenomenex C,8 (4.6 mm×250 mm, 5 μm), acetonitrile-0.1% phosphoric acid (0-40 min, acetonitrile 20%--45% ) as mobile phase, and the flow rate was 1.0 mL/min, the wave- length were maximum absorption wavelength according to every component respectively. Results: Liquiritin, lobetyolin, baicalin and baicalein showed good linear relationship in the range between 0.05-0.75μg, 0.042-0.63 μg, 0.80-12.0 μg and 0.04-0.60 μg respectively. Correlation coefficients were 0.9995, 0.9992, 0.9999 and 0.9997, aver-age recovery rates were 100.31%, 98.92%, 101.06% and 100.17%, RSD% were 1.90, 1.63, 2.21 and 1.19. Conclusion: The method, stable, reliable and easy to operate, could solve the problem that lobetyolin is too low to detect.
出处
《西部中医药》
2017年第1期26-28,共3页
Western Journal of Traditional Chinese Medicine
基金
2013年兰州市第三批科技计划项目(编号2013-3-54)