Peak shape distortions during capillary electrophoretic separations of multicomponent samples in two co-ion buffers

被引:19
作者
Williams, RL
Childs, B
Dose, EV
Guiochon, G
Vigh, G
机构
[1] TEXAS A&M UNIV,DEPT CHEM,COLLEGE STN,TX 77843
[2] TEXAS A&M UNIV,DEPT COMP SCI,COLLEGE STN,TX 77843
[3] UNIV TENNESSEE,DEPT CHEM,KNOXVILLE,TN 37996
关键词
quaternary ammonium compounds; computer simulation; background electrolyte composition; peak shape;
D O I
10.1016/S0021-9673(97)00509-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
During the capillary electrophoretic separation of a five-component quaternary ammonium analyte sample in two co-ion background electrolytes prepared from phosphoric acid, lithium hydroxide and tetrabutylammonium hydroxide, grossly distorted analyte peaks were observed. The electropherograms were successfully simulated using an earlier mathematical model of electrophoresis that was extended to handle up to eight nonproteic sample ions and two nonproteic background electrolyte co-ions. Peak shape distortion closely followed the predictions made during the recently described simulations of single analyte-two co-ion background electrolyte systems. Peak shape distortion was shown to depend on the relative mobilities of the particular analyte, the non-comigrating system peak and the governing co-ion. Severe peak shape distortion could occur in every multiple co-ion background electrolyte, such as in the indirect detection background electrolytes and charged interacting agent-containing background electrolytes, when certain analyte peaks and the non-comigrating system peaks overlap. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:107 / 112
页数:6
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