On-column formation of arsenic-glutathione species detected by size-exclusion chromatography in conjunction with arsenic-specific detectors

被引:54
作者
Gailer, J
Lindner, W
机构
[1] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[2] Univ Vienna, Inst Analyt Chem, A-1090 Vienna, Austria
来源
JOURNAL OF CHROMATOGRAPHY B | 1998年 / 716卷 / 1-2期
基金
奥地利科学基金会;
关键词
arsenite; glutathione;
D O I
10.1016/S0378-4347(98)00282-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The 'retention analysis method', which is based on size-exclusion chromatography (SEC) in conjunction with an arsenic-specific detector (graphite furnace atomic absorption spectrometer, GFAAS), was used to study the effect of pH (range 2.0-10.0), temperature (4, 25 and 37 degrees C), and the concentration of glutathione in the mobile phase (0.5-7.5 mM) on the formation of arsenic-glutathione species after injection of sodium arsenite using phosphate-buffered saline solutions as mobile phases. The formation of arsenic-GSH species was facilitated by low temperatures (4 degrees C), pH 6.0-8.0 and high concentrations of glutathione (7.5 mM) in the mobile phase. Simulating the physicochemical parameters found inside human red blood cells (similar to 3.0 mM glutathione, 37 degrees C, pH 7.4) and hepatocytes (similar to 7.5 mM glutathione, 37 degrees C, pH 7.4), SEC-GFAAS provided evidence for the formation of arsenic-glutathione species under these conditions. In addition, the 'chelating agent', sodium DL-2,3-dimercapto-1-propanesulfonate (1.0 and 2.0 mM) was demonstrated to bind arsenous acid stronger in the presence of glutathione (7.5 mM) under these conditions (PBS buffer, pH 7.4, 37 degrees C). (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:83 / 93
页数:11
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