Chinese Journal of Applied Chemistry ›› 2011, Vol. 28 ›› Issue (11): 1340-1342.DOI: 10.3724/SP.J.1095.2011.00023

• Communications • Previous Articles    

Chiral Separation of Enantiomers of Four Amino Acids and Two Chial Drugs Through Capillary Electrophoresis

ZHANG Chunyu, LI Yingjie*, HAO Xiuju, GAO Qing   

  1. (College of Chemistry and Chemical Engineering,Qiqihar University,Qiqihar 161006)
  • Received:2011-01-13 Revised:2011-04-11 Published:2011-11-10 Online:2011-11-10
  • Contact: chunyu Zhang

Abstract:

Enantiomers of amino acids and chiral drugs were separated by capillary zone electrophoresis using double (6-O-β-carboxy-methyl-1,4-maleic acid ester)-β-cyclodextrin(DOCB-β-CD) as chiral selector. The buffer solution used was 20 mmol/L phosphate. The influences of DOCB-β-CD concentration, background buffer pH value, temperature and applied voltage were investigated. Under the respective optimum condition, enantiomers separation of four kinds of DL-amino acids(Phenylalanine, Tryptophan, Tyrosine and Histidine) and two kinds of chiral drugs(rofecoxib and rosiglitazone) were attained with a clear separation from the baseline.

Key words: Capillary electrophoresis, β-cyclodextrin derivative, DL-amino acid, chiral drugs

CLC Number: