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- W2371895114 abstract "Objective:To separate and determine ginsengnoside Rg_1,ginsengnoside Re and notoginsengnoside R_1 from Radix et Rhizoma Notoginseng.Method:Experiments were performed on Beckman P/ACE MDQ capillary e- lectrophoresis system,the fused-sillica capillary tube was used with 20 mmol·L~(-1) SDS,40 mmol·L~(-1) sodium cholata,60 mmol·L~(-1) Na_2B_4O_7.The dimersion of the capillary columns was 50 μm×40 cm,30 cm from the inlet to the detection window,on-line UV detector was operated at 200 nm.Results:Under optimum condition,the re- coveries of the analytes in the extact of Radix notoginseng in low,medial,high level was 101.5%,100.6%, 100.4% and the RSD was 2.4%,2.2%,1.0% for ginsengnoside Rg_1,in low,medial,high level was 101.3%, 99.23%,99.66%,and the RSD was 2.0%,1.3%,1.1% for ginsengnoside Re,and in low,medial,high level was 100.6%,100.5%,100.7%,and the RSD was 1.1%,1.1%,0.86% for notoginsengnoside R_1 respectively.Con- clusion:The optimum method puts up a good reproducibility,high accuracy and great linear,which meets the re- quest of analysis.The results show that the method can be used to control quality of Radix et Rhizoma Notoginseng." @default.
- W2371895114 created "2016-06-24" @default.
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- W2371895114 date "2007-01-01" @default.
- W2371895114 modified "2023-09-23" @default.
- W2371895114 title "Separation and determination of ginsengnoside Rg_1,ginsengnoside Re and notoginsengnoside R_1 from Radix et Rhizoma Notoginseng by micellar electrokinetic chromatography" @default.
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