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Research articles
Research articles
6-O-(2-hydroxybutyl)-β-CD as a chiral selector
for nonaqueous capillary electrophoretic separation of chiral drugs
- Wenguo XING1,Yunhe WEI1,Ping YU1,Changqiao ZHANG1,Jian LI2,
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1.School ofChemistry and
Chemical Engineering, Shandong University, Jinan 250100, China; 2.Shandong Analyses and
Test Center, Jinan 250014, China;
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History
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Published |
05 Dec 2009 |
Issue Date |
05 Dec 2009 |
Abstract
6-O-(2-hydroxybutyl)-β-CD, as a new β-cyclodextrin (β-CD) derivative, was successfully synthesized. It was used as a chiral selector to separate six chiral drugs, including propranolol, anisodamine, promethazine, ketoconazole, benzhexol, and fenfluramine in nonaqueous capillary electrophoresis (NACE). The effects of the organic solvent, the electrolytes, the concentrations of cyclodextrin derivatives, and the pH of the buffer on the chiral resolution (Rs) were investigated. The baseline separation of enantiomers, including propranolol (Rs=2.26), anisodamine (Rs=2.31), promethazine (Rs=2.42), ketoconazole (Rs=2.56), benzhexol (Rs=3.38), and fenfluramine (Rs=3.04), could be achieved using a buffer of 100 mmol·L−1 citric acid and 50 mmol·L−1 Tris (hydroxymethyl) aminomethane (Tris) at pH 4.6 containing 100 mmol·L−1 6-O-(2-hydroxybutyl)-β-CD in formamide (FA).
Keywords
nonaqueous capillary electrophoresis /
enantiomer separation /
β-cyclodextrin derivatives /
chiral drugs
Cite this article
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Wenguo XING, Yunhe WEI, Ping YU, Changqiao ZHANG, Jian LI,.
6-O-(2-hydroxybutyl)-β-CD as a chiral selector
for nonaqueous capillary electrophoretic separation of chiral drugs. Front. Chem. China, 2009, 4(4): 396‒401 https://doi.org/10.1007/s11458-009-0038-3
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