Enantioseparation of amino alcohol drugs by nonaqueous capillary electrophoresis with a maltobionic acid-based ionic liquid as the chiral selector

The Analyst ◽  
2019 ◽  
Vol 144 (24) ◽  
pp. 7468-7477 ◽  
Author(s):  
Xiaofei Ma ◽  
Zigui Kan ◽  
Yingxiang Du ◽  
Jiangxia Yang ◽  
Zijie Feng ◽  
...  

This study deals with the nonaqueous capillary electrophoretic enantioseparation of twenty-two amino alcohol drugs with a maltobionic acid (MA)-based ionic liquid (tetramethylammonium maltobionic acid, TMA-MA) as the novel chiral selector.

2014 ◽  
Vol 35 (23) ◽  
pp. 3310-3316 ◽  
Author(s):  
Yuanqi Lu ◽  
Dunqing Wang ◽  
Chunyan Kong ◽  
Hao Zhong ◽  
Michael C. Breadmore

2014 ◽  
Vol 35 (19) ◽  
pp. 2759-2764 ◽  
Author(s):  
Margarita V. Lebedeva ◽  
Aleksandra F. Prokhorova ◽  
Elena N. Shapovalova ◽  
Oleg A. Shpigun

Author(s):  
Xiaofei Ma ◽  
Jingtang Li ◽  
Xiaoqi Li ◽  
Zijie Feng ◽  
Xuan Yang ◽  
...  

Abstract Nowadays, ionic liquids (ILs) functionalized cyclodextrins (CDs) have drawn increasing attention in chiral separation. Herein, a novel β-CD derivative functionalized by L-histidinium IL, mono-6-deoxy-6-L-histidinium-β-cyclodextrin chloride (L-HMCDCl), was synthesized for the first time and utilized for enantioseparation of nefopam and chlorphenamine in capillary electrophoresis. The L-HMCDCl exhibited superior enantioselectivity compared with native β-CD. The effect of some key parameters such as chiral selector concentration, buffer pH and applied voltage on the enantioseparation was investigated in detail. In the interest of the chiral discrimination mechanism and the enhanced enantioselectivity of L-HMCDCl, molecular modeling with AutoDock was employed to study the interaction, which was in good agreement with experimental results.


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