Synergistic chiral separations using the glycopeptides ristocetin A and vancomycin

被引:17
作者
Ward, TJ [1 ]
Farris, AB [1 ]
Woodling, K [1 ]
机构
[1] Millsaps Coll, Dept Chem, Jackson, MS 39210 USA
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2001年 / 48卷 / 02期
关键词
enantioseparations; capillary electrophoresis; chiral; vancomycin; ristocetin A;
D O I
10.1016/S0165-022X(01)00147-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The effectiveness of using a mixture of the chiral selectors vancomycin and ristocetin A to achieve chiral recognition was examined in this study. The results of using the mixed chiral selector vancomycin and ristocetin A in capillary electrophoresis were compared with the results of using each chiral selector alone. Chiral separations were carried out using a coated capillary column to suppress electroosmotic flow and minimize interactions with the capillary wall. We employed a countercurrent process where the solute reaches the detection cell window after the chiral selector has cleared the window, minimizing the background absorbance from the chiral selector and improving sensitivity. Using a mixture of vancomycin and ristocetin A, separations were achieved which often exceeded the resolving power of tither chiral selector when used alone. The effect of voltage on resolution was also studied, and the optimal voltage was found to be between -5 and - 8 kV. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:163 / 174
页数:12
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