Separation and Determination of Salidroside, Caffeic Acid and Gallic Acid in Rhodiola L. by Large-Volume Sample Stacking-Sweeping-Micellar Electrokinetic Chromatography

被引:0
作者
Huang, Wen-Yi [1 ]
Li, Li-Jun [1 ]
Hu, Da-Chun [1 ]
Wu, Mei-Yan [1 ]
Gao, Wen-Yan [2 ]
Lai, Ying-Biao [1 ]
Li, Yan-Qing [1 ]
机构
[1] Guangxi Univ Technol, Dept Biol & Chem Engn, Liuzhou 545006, Guangxi, Peoples R China
[2] Guangxi Univ, Coll Chem & Chem Engn, Nanning 530004, Guangxi, Peoples R China
关键词
Micellar electrokinetic chromatography; Electrostacking; Large volume sample stacking; Sweeping; Salidroside; Caffeic acid; Gallic acid; CAPILLARY-ELECTROPHORESIS; PRECONCENTRATION;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, a new method for simultaneous determination of salidroside, caffeic acid and gallic acid in Rhodiola L. by large volume sample stacking-Sweeping micellar electrokinetic chromatography (LVSS-sweeping-MEKC) has been proposed. The determination conditions containing pH in background solution, concentrations of Na2B4O7, sodium dodecyl sulfate (SDS) and acetonitrile, injection time, negative voltage and separation voltage were optimized. The operating buffer was composed of 20 mmol/L Na2B4O7, 80 mmol/L sodium dodecyl sulfate and 10 % (by volume) acetonitrile at pH 9.7 with a constant temperature of 25 degrees C. The UV detection wavelength was 213 nm, the reverse voltage was -8 kV, separation voltage was 20 kV and injection time was 120 s. The linear ranges of the method were 13.1-49.6 mu g/L for salidroside, 1.0-15.7 mu g/L for caffeic acid and 1.1-18.2 mu g/L for gallic acid. The recoveries were 95-106, 98-112 and 91-108 %, respectively. The RSDs of peak area were less than 4 % and detection limits (S/N = 3) were 194, 28 and 29 mu g/L for salidroside, caffeic acid and gallic acid respectively.
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收藏
页码:2155 / 2158
页数:4
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