Enantioseparation of o-phthaldiadehyde derivatized amino acids using beta-CD-modified micellar electrokinetic chromatography in the mixed aqueous-organic media
Ll. Yang et al., Enantioseparation of o-phthaldiadehyde derivatized amino acids using beta-CD-modified micellar electrokinetic chromatography in the mixed aqueous-organic media, ANALYT CHIM, 433(1), 2001, pp. 23-30
A method for the enantioseparation of amino acids derivatized with o-phthal
diadehyde (OPA) and N-acylated cysteine (AC) using beta -cyclodextrin (beta
-CD)-modified micellar electrokinetic chromatography (MEKC) in the presenc
e of organic modifier was developed. The effects of separation parameters,
such as the pH Value of the buffer, the concentration of the buffer, beta -
CD bile salt and organic modifiers, on the migration times and resolutions
of chiral amino acids were investigated and the optimum experimental condit
ions were 40 mmol l(-1) borax (pH 9.0), 60 mmol l(-1) sodium taurocholate (
STC), 30 mmol l(-1) beta -CD and 15% (v/v) of isopropanol (IPA). Using the
proposed method, 11 pairs of OPA/AC-DL-amino acids were separated simultane
ously with the resolution ranging from 1.038 to 3.367 in less than 19 min.
(C) 2001 Elsevier Science B.V. All rights reserved.