Chinese Journal of Applied Chemistry ›› 2011, Vol. 28 ›› Issue (11): 1340-1342.DOI: 10.3724/SP.J.1095.2011.00023
• Communications • Previous Articles
ZHANG Chunyu, LI Yingjie*, HAO Xiuju, GAO Qing
Received:
Revised:
Published:
Online:
Contact:
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:
O657
ZHANG Chunyu, LI Yingjie*, HAO Xiuju, GAO Qing. Chiral Separation of Enantiomers of Four Amino Acids and Two Chial Drugs Through Capillary Electrophoresis[J]. Chinese Journal of Applied Chemistry, 2011, 28(11): 1340-1342.
0 / / Recommend
Add to citation manager EndNote|Ris|BibTeX
URL: http://yyhx.ciac.jl.cn/EN/10.3724/SP.J.1095.2011.00023
http://yyhx.ciac.jl.cn/EN/Y2011/V28/I11/1340