Some factors affecting separation and detection of amino acids by high-performance anion-exchange chromatography with integrated pulsed amperometric detection

被引:24
|
作者
Yu, H
Ding, YS
Mou, SF
机构
[1] Acad Sinica, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
[2] Harbin Normal Univ, Dept Chem, Harbin 150080, Peoples R China
关键词
mobile phase composition; temperature effects; detection; LC; integrated pulsed amperometric detection; electrochemical detection; amino acids;
D O I
10.1016/S0021-9673(03)00116-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Some factors influencing the separation and detection of amino acids by high-performance anion-exchange chromatography with integrated pulsed amperometric detection were investigated. These factors include eluent concentration, column temperature, and detection waveform. The selectivity changes in weakly retained amino acids are slight with changing sodium hydroxide eluent concentration. When sodium acetate eluent concentration is changed, the selectivity variations between strongly retained amino acids containing two carboxyl groups and containing only one carboxyl group are obviously different. Significant but slight selectivity changes in weakly retained amino acids can be achieved through changing the column temperature. Sodium hydroxide and sodium acetate eluent concentration affect the detection of amino acids. Detection sensitivity of amino acids can be improved by increasing the concentration of sodium hydroxide and sodium acetate in a certain concentration range. The detections of amino acids at two different detection waveforms were compared. The hydroxyl amino acids can be selectively detected by choosing a modified detection waveform. The optimized gradient elution condition and column temperature for analyzing 19 amino acids were obtained. The time for the gradient elution program was 60 min. The column temperature was 35degreesC. Under the optimized conditions, detection limits for 19 amino acids were 0.15-4.52 pmol. The calibration graphs of peak area for all the analytes were linear for about three orders of magnitude. The RSDs (n = 5) of peak area were 0.6-5.6%. The determination of trace amino acid impurities in valine product is shown as an application example. (C) 2003 Elsevier Science B.V. All rights reserved.
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页码:145 / 153
页数:9
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