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作 者:朱莹莹[1] 刘鑫[1] 贾艾玲[1] 王琳[1] 邱智东[1] 朱凯[1]
机构地区:[1]长春中医药大学,长春130117
出 处:《中国实验方剂学杂志》2016年第7期96-99,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家科技支撑计划项目(2012BAI29B05);吉林省科技厅项目(20130206025YY)
摘 要:目的:建立一种可以同时测定人参药性菌质中8种人参皂苷(人参皂苷Rg1,人参皂苷Re,人参皂苷Rf,人参皂苷Rh1,人参皂苷Rb1,人参皂苷Ro,人参皂苷Rb2,人参皂苷Rd)含量的HPLC方法。方法:采用高效液相法,Inertsil ODS-SP色谱柱(4.6 mm×250 mm,5μm),流动相乙腈-0.4%磷酸水梯度洗脱,流速1 m L·min-1,检测波长203 nm,柱温30℃,测定人参药性菌质8种皂苷的含量。结果:8种单体皂苷在100 min内可良好分离,线性关系良好(R2>0.999 7),平均加样回收率分别为100.15%,101.54%,101.87%,100.88%,102.10%,102.84%,101.38%,101.23%,RSD分别为1.6%,2.3%,1.9%,2.1%,1.5%,0.8%,2.7%,1.6%。结论:该研究提供了一种能方便、简单、准确、重复性好的HPLC分析人参药性菌质中8种人参皂苷含量的方法,可为人参药性菌质成分转化研究的质量标准制定提供科学依据。Objective: To establish an HPLC method for simultaneous determination of ginsenoside Rg1,ginsenoside Re, ginsenoside Rf, ginsenoside Rh1,ginsenoside Rb1,ginsenoside Ro,ginsenoside Rb2,and ginsenoside Rd in ginseng medicinal fungal substance. Method: High performance liquid chromatography was carried out on Inertsil ODS-SP chromatographic column( 4. 6 mm × 250 mm,5 μm) with acetonitrile-0. 4%phosphate as the mobile phase for gradient elution. The flow rate was 1 m L·min- 1,and detection wavelength was203 nm. The column temperature was at 30 ℃. Result: Eight kinds of monomer saponins could be separated well in 100 min, with good linear relationship( R2 〉0. 999 7). The average recovery rate was 100. 15%( RSD1. 6%),101. 54%( RSD 2. 3%),101. 87%( RSD 1. 9%),100. 88%( RSD 2. 1%),102. 10%( RSD1. 5%),102. 84%( RSD 0. 8%),101. 38%( RSD 2. 7%),and 101. 23%( RSD 1. 6%). Conclusion: The HPLC method is accurate,reliable and reproducible to analyze 8 saponins in ginseng medicinal fungal substance,which can provide the scientific basis for formulating the quality standard of the research on composition transformation of the ginseng medicinal fungal substance.
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