Voltammetric detection for capillary electrophoresis

被引:25
作者
Park, S
McGrath, MJ
Smyth, MR
Diamond, D
Lunte, CE
机构
[1] UNIV KANSAS,DEPT CHEM,LAWRENCE,KS 66045
[2] UNIV KANSAS,CTR BIOANALYT RES,LAWRENCE,KS 66045
[3] DUBLIN CITY UNIV,SCH CHEM SCI,DUBLIN 9,IRELAND
关键词
D O I
10.1021/ac970156q
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Several approaches to implementing amperometric detection for capillary electrophoresis have been reported. This report describes the development of a voltammetric detector for CE. The detector is designed to minimize distortion of the voltammetry due to ohmic potential drop. This was accomplished by using a cast Nafion detection cell at the end of the separation capillary. The cast Nafion detection cell provided a low-dead-volume, low-resistance cell that minimized ohmic potential drop and peak band broadening. The ability to detect the current due to oxidation of analytes superimposed on a large background current was also improved. A dynamic background subtraction scheme was used in which a second working electrode, positioned in the electrochemical cell but outside of the detection cell, was used to compensate for the background current in realtime. The output of the compensating working electrode was subtracted from the output of the detecting working electrode prior to analog-to-digital conversion. Postexperimental digital background subtraction was also implemented. This approach provided optimal elimination of the background current with maximal detection of the analytical signal. The voltammetric detector developed produced high-quality voltammetric response of analytes with injected concentrations as low as 0.20 mu M. The system was evaluated by obtaining CE voltammograms of a mixture of eight test phenolic acids.
引用
收藏
页码:2994 / 3001
页数:8
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