Simultaneous determination of oxalate, thiosulfate, and thiocyanate in urine by ion-exclusion chromatography with electrochemical detection

被引:11
作者
Xu, JM
Wang, YP
Xian, YZ
Li, H
Jin, LT [1 ]
Tanaka, K
Haraguchi, H
Itoh, A
机构
[1] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
[2] Natl Ind Res Inst Nagoya, Kita Ku, Nagoya, Aichi 4628510, Japan
[3] Nagoya Univ, Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 4648603, Japan
关键词
column liquid chromatography; ion-exclusion chromatography; amperometric detection; oxalate; thiosulfate; and thiocyanate in urine;
D O I
10.1007/BF02492008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive ion-exclusion chromatographic method has been developed for determination of oxalate, thiosulfate, and thiocyanate. The method is based on separation of these anions on a polymethacrylate-based, weakly acidic cation-exchange resin (TSKgel OApak-A) and detection by means of a glassy carbon (GC) electrode electrochemically modified with polyvinylpyridine (PVP), palladium, and iridium oxide (PVP/Pd/IrO2). The electrochemical behavior of oxalate, thiosulfate, and thiocyanate at this chemically modified electrode (CME) have been investigated by cyclic voltammetry The results indicated that electrocatalytic oxidation of these anions by the electrode was efficient and that the sensitivity stability, and lifetime of the electrode were relatively high. Combined with ion-exclusion chromatography the PVP/Pd/IrO2 electrode was used as the working electrode for amperometric detection of these anions. All linear ranges were over two orders of magnitude and detection limits, defined as S/N = 3, were 9.0 x 10(-7) mol L-1 for oxalate, 6.7 x 10-7 mol L-1 for thiosulfate, and 5.6 x 10(-7) mol L-1 for thiocyanate. Correlation coefficients were all > 0998. Coupled with microdialysis sampling the method has been successfully applied to the determination of oxalate, thiosulfate, and thiocyanate in urine.
引用
收藏
页码:449 / 453
页数:5
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