摘要
目的建立HPLC同时定量测定采自西藏、四川阿坝毛果婆婆纳中梓醇、桃叶珊瑚苷、胡黄连苷Ⅱ的方法。方法采用外标法,Gemini C18色谱柱(110,4.60 mm×250 mm,5μm),流动相为乙腈(A)-水(B)梯度洗脱(0-13 min,3%A;13-20 min,3%-15%A;20-50 min,15%A;50-60 min,15%-21%A;60-70 min,21%A;70-110 min,21%-100%A),体积流量1.0 m L/min,柱温25℃,检测波长203 nm。结果梓醇、桃叶珊瑚苷、胡黄连苷Ⅱ的线性范围分别为0.101 5-5.076μg,0.093 2-4.66μg,0.043 6-2.18μg;平均加样回收率分别为98.9%(RSD 1.0%),103.8%(RSD 0.7%),98.8%(RSD 1.9%)。结论 10个产地婆婆纳中梓醇、桃叶珊瑚苷、胡黄连苷Ⅱ的量差异明显,高低差异近10倍之多。
AIM To develop a method for determining catalpol,aucubin and picroside Ⅱ from Veronica eriogyne H. Winkl collected from Tibet and Si'chuan Province by HPLC. METHODS External standard method and the chromatographic Gemini C18 Column( 110 ,4. 60 mm × 250 mm,5 μm) were adopted with mobile phase consisting of acetonitrile( A)-water( B) in a gradient elution manner. The detected wavelength was set up at 203 nm and column temperature was maintained at 25 ℃. RESULTS The linear ranges were 0. 101 5- 5. 076μg for catalpol,0. 093 2- 4. 66 μg for aucubin,and 0. 043 6- 2. 18 μg for picroside Ⅱ,respectively. The average recoveries of catalpol,aucubin and picroside Ⅱ were 98. 9%( RSD 1. 0%),103. 8%( RSD 0. 7%) and98. 8%( RSD 1. 9%),respectively. CONCLUSION The differences of contents of three constituents from V.eriogyne H. Winkl collected from ten growing areas are large,almost tenfold.
出处
《中成药》
CAS
CSCD
北大核心
2015年第4期810-813,共4页
Chinese Traditional Patent Medicine
基金
四川省科技厅基本科研业务专项基金资助项目(A-2014N-10)