摘要
目的:建立HPLC-DAD测定茵陈蒿汤中儿茶素、绿原酸、西红花苷Ⅰ、西红花苷Ⅱ含量的方法。方法:采用Symmetry C18色谱柱(4.6mm×250mm,5μm),流动相乙腈-0.1%磷酸水梯度洗脱,流速1.0mL·min-1,柱温30℃,儿茶素检测波长202nm,绿原酸检测波长330nm,西红花苷Ⅰ,Ⅱ检测波长440nm。结果:儿茶素、绿原酸、西红花苷Ⅰ,Ⅱ分别在0.18-0.9(r=0.999 8),0.062 4-0.312(r=0.999 9),0.441-2.205(r=0.999 9),0.023 52-0.117 6μg(r=0.999 9)与峰面积呈良好线性关系;加样回收率分别为98.56%(RSD 1.8%),99.07%(RSD 1.8%),97.41%(RSD 1.9%)和98.46%(RSD1.9%)。结论:该法简便、准确、专属性强,可用于茵陈蒿汤中4种成分的含量测定。
Objective: To establish a method for simultaneous determination of catechin,chlorogenic acid,crocin-Ⅰ,and crocin-Ⅱ in Yinchenhao decoction by HPLC-DAD.Method: The Symmetry C18 column(4.6mm × 250mm,5μm) was used,the mobile phase was acetonitrile-0.1% phosphoric acid solution with gradient elution at a flow rate of 1.0 m L·min-1.The column temperature was kept at 30 ℃ and the wavelength was set at 202nm for catechin,330nm for chlorogenic acid,and 440nm for crocin-Ⅰand crocin-Ⅱ,respectively.Result: The linear range of catechin,chlorogenic acid,crocin-Ⅰ,and crocin-Ⅱ were 0.18-0.90(r = 0.999 8),0.020 8-0.374 4(r = 0.999 9),0.147-2.646(r = 0.999 9) and 0.007 84-0.141 12(r = 0.999 9)μg,respectively.The mean recovery of these 4 components were 98.56%(RSD 1.8%),99.07%(RSD 1.8%),97.41%(RSD 1.9%),and 98.46%(RSD 1.9%),respectively.Conclusion: This method is simple,accurate and specific,and can be used for the determination of 4 constituents in Yinchenhao decoction.
出处
《中国实验方剂学杂志》
CAS
CSCD
北大核心
2015年第6期48-51,共4页
Chinese Journal of Experimental Traditional Medical Formulae
基金
江苏省中医药局科技项目(HZ07071)
江苏省高校自然科学基金项目(08KJB360009)