Capillary electrophoresis with constant potential amperometric detection using a nickel microelectrode for detection of carbohydrates
被引:0
|
作者:
Fermier, AM
论文数: 0引用数: 0
h-index: 0
机构:
SUNY BUFFALO,NAT SCI & MATH COMPLEX,DEPT CHEM,BUFFALO,NY 14260SUNY BUFFALO,NAT SCI & MATH COMPLEX,DEPT CHEM,BUFFALO,NY 14260
Fermier, AM
[1
]
Colon, LA
论文数: 0引用数: 0
h-index: 0
机构:
SUNY BUFFALO,NAT SCI & MATH COMPLEX,DEPT CHEM,BUFFALO,NY 14260SUNY BUFFALO,NAT SCI & MATH COMPLEX,DEPT CHEM,BUFFALO,NY 14260
Colon, LA
[1
]
机构:
[1] SUNY BUFFALO,NAT SCI & MATH COMPLEX,DEPT CHEM,BUFFALO,NY 14260
来源:
HRC-JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY
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1996年
/
19卷
/
11期
关键词:
capillary electrophoresis;
electrochemical detection;
end column detection;
nickel electrode;
carbohydrates;
D O I:
暂无
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Carbohydrates were separated by capillary electrophoresis (CE) and detected electrochemically using a nickel microelectrode which was operated at a constant applied potential (similar to 0.6 V vs. Ag/AgCl). A simple capillary electrode holder design facilitated alignment between the separation capillary and the working microelectrode without the use of micro-positioning equipment. The separations were performed under alkaline conditions (pH > 11), matching the high pH requirements for amperometric detection at the nickel electrode. The analytical procedure developed showed detection limits for the carbohydrates studied in the micromolar range, showing a linear response in the range tested (micromolar to millimolar). The procedure was used to identify sugars in two real samples (i.e., urine and in a common beverage). The potential use of the system for the determination of amino acids was also demonstrated.