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Chiral separation of benzothiazole derivatives of amino acids using capillary zone electrophoresis
被引:14
|作者:
Novakova, Zuzana
[1
]
Pejchal, Vladimir
[2
]
Fischer, Jan
[1
]
Cesla, Petr
[1
]
机构:
[1] Univ Pardubice, Fac Chem Technol, Dept Analyt Chem, Studentska 573, CZ-53210 Pardubice, Czech Republic
[2] Univ Pardubice, Fac Chem Technol, Inst Organ Chem & Technol, Pardubice, Czech Republic
关键词:
amino acids;
benzothiazole derivatives;
capillary zone electrophoresis;
dual cyclodextrin systems;
polydimethylacrylamide-coated capillaries;
STRUCTURAL-CHARACTERIZATION;
BETA-CYCLODEXTRIN;
ENANTIOSEPARATION;
INHIBITORS;
SELECTORS;
D O I:
10.1002/jssc.201600689
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
A method for the separation of enantiomers of leucine and phenylalanine benzothiazole derivatives as potential antimicrobial agents was developed using capillary zone electrophoresis with a dual cyclodextrin (CD) system. The best resolution of enantiomers was achieved in 100 mmol/L phosphate background electrolyte (pH 3.5) with the dual CD system consisting of 10 mmol/L of beta-CD with 10 mmol/L of 2-hydroxypropyl-beta-cyclodextrin for leucine derivative and 10 mmol/L of 2-hydroxypropyl-gamma-cyclodextrin for phenylalanine derivative, respectively. Under the optimal conditions, the highest enantioresolution of 1.25 was achieved in a noncoated-fused silica capillary at 17 degrees C and 24 kV applied voltage.
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页码:798 / 803
页数:6
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