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高效毛细管电泳地测定中草药川乌,草乌中乌头碱的含量
引用本文:孙爱民,陈德华.高效毛细管电泳地测定中草药川乌,草乌中乌头碱的含量[J].色谱,1999,17(1):67-69.
作者姓名:孙爱民  陈德华
作者单位:[1]华西医科大学分析测试中心 [2]香港中文大学化学系
摘    要:建立了测定有毒中草药川乌和草乌中3种乌头碱的高效毛细管电泳方法,系统地考察了电泳条件对分离的影响,并应用于香港市售川乌及草乌中中乌头碱、次乌头碱和乌头碱的测定,检测限为1.67-2.31mg/L,回收率为93.0-104.0%,相对标准差为0.68-1.70%。

关 键 词:HPLC  中乌头碱  次乌头碱  乌头碱  川乌  草乌  测定

Determination of the aconitine alkaloids in traditional Chinese medicine chuanwu and caowu by high performance capillary electrophoresis(HPCE)]
A Sun,D Chen,P Bi.Determination of the aconitine alkaloids in traditional Chinese medicine chuanwu and caowu by high performance capillary electrophoresis(HPCE)][J].Chinese Journal of Chromatography,1999,17(1):67-69.
Authors:A Sun  D Chen  P Bi
Institution:Analytical Test Center, West China University of Medical Sciences, Chengdu, 610041.
Abstract:A simple and rapid method for the simultaneous assay of three aconitine alkaloids (mesaconitine (MA), hypaconitine (HA) and aconitine (A) in the traditional Chinese medicines, Chuanwu and Caowu, by high performance capillary electrophoresis has been established, using tetracaine as an internal standard. The experimental conditions were as follows, the electrophoretic medium was composed of V70 mmol/L Tris-borate (pH 8.49)]: V(methanol) = 60:40, uncoated capillary used was 50 cm x 50 microns i.d. and detection was carried out with a UV monitor at 235 nm. The separation was achieved by optimizing the cartridge temperature, the applied voltage, and the pH as well as the concentration of the buffer, and organic modifier. The calibration curve showed a good linearity in the mass concentration range of 0.0115-0.8330 g/L (r = 0.9996) for MA, 0.0089-0.6440 g/L (r = 0.9997) for HA, and 0.0083-0.6000 g/L(r = 0.9997) for A. The recoveries ranged from 93.0% to 104.0% with relative standard deviations from 0.68% to 1.7%. The total time for separation and determination was within 23 min. By means of this method, three aconitine alkaloids in Chuanwu and Caowu have been determined.
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