Application of carboxymethyl-beta-cyclodextrin as a chiral selector in capillary electrophoresis for enantiomer separation of selected neurotransmitters
W. Maruszak et al., Application of carboxymethyl-beta-cyclodextrin as a chiral selector in capillary electrophoresis for enantiomer separation of selected neurotransmitters, J CHROMAT A, 926(2), 2001, pp. 327-336
The aim of this work was to optimize conditions for capillary electrophores
is separation of different neurotransmitters (serotonin, phenylalanine, dop
amine, adrenaline, ephedrine, propranolol and DOPA) in a single run, includ
ing separation of existing enantiomers. As chiral selectors added to the bo
rate background, electrolyte unsubstituted alpha-, beta- and gamma -cyclode
xtrins (CDs), methyl-, dimethyl-, and trimethyl-substituted beta -CDs, and
hydroxypropyl-substituted alpha-, beta- and gamma -CDs were examined. Also
carboxymethyl-beta -CD and succinyl-beta -CD were used for this purpose. In
addition to the kind and concentration of chiral selector, some other expe
rimental factors also have been optimized, such as concentration of borate
buffer, content of methanol, pH of electrolyte, method of sample introducti
on into the capillary and washing procedure between consecutive runs. The b
est results were obtained using 20 trild carboxymethyl-beta -CD in borate b
uffer of pH 7.5 as running electrolyte and hydrostatic injection. The obtai
ned sensitivity of response (peak height) varied from 0.4 for adrenalines t
o 2.3 mAU mM(-1) for propranolols. The concentration detection limits (S/N=
3) were in the range from 0.04 mM for propranolols to 0.2 mM for adrenaline
s. The resolution obtained in optimized conditions in a single run was from
0.75 for adrenalins and 1.0 for propranolols up to 2.0 for ephedrines. The
developed method was employed for determination of these analytes in brain
tissue extracts. (C) 2001 Elsevier Science B.V. All rights reserved.