Separation of monomethyl-benz[a]anthracene isomers using cyclodextrin-modified electrokinetic chromatography

Citation
C. Akbay et al., Separation of monomethyl-benz[a]anthracene isomers using cyclodextrin-modified electrokinetic chromatography, J CHROMAT A, 910(1), 2001, pp. 147-155
Citations number
44
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
Volume
910
Issue
1
Year of publication
2001
Pages
147 - 155
Database
ISI
SICI code
Abstract
Cyclodextrin-modified electrokinetic chromatography (CD-EKC) was investigat ed for the separation of 12 mono-methylbenz[a]anthracene (MBA) isomers. Com bined use of a polymeric surfactant, poly(sodium 10-undecenyl sulfate) (pol y-SUS), with various types of neutral cyclodextrins (CDs) [beta -CD, gamma -CD, dimethyl-beta -CD (DM-beta -CD), trimethyl-beta -CD (TM-beta -CD) and hydroxypropyl-beta -CD (HP-beta -CD)] were successful in CD-EKC separation of the MBA isomers. Baseline resolution of 10 of the 12 isomers, except for 9-MBA and 2-MBA, was achieved with gamma -CD at pH 9.75. The beta -CD, gam ma -CD, and beta -CD derivatives (DM-beta -CD, TM-beta -CD, HP-beta -CD) we re found to have different resolution and selectivity. Additionally, the t( R)/t(O) values of isomers were found to be dependent on the type and concen tration of the CD additives. In general, t(R)/t(O) values of MBA isomers de crease with an increase in the concentration of beta -CD derivatives, where as the reversed was true when the concentrations of native beta -CD and gam ma -CD were varied. The combination of 5 mM gamma -CD, 0.5% (w/v) poly-SUS, 35% (v/v) acetonitrile at a pH of 9.75 provided the best selectivity and r esolution of the MBA isomers with a separation time of 110 min. However, th e use of 30 mM DM-beta -CD under similar EKC conditions resulted in much fa ster separation (ca. 16 min) of 10 MBA isomers. (C) 2001 Elsevier Science B .V. All rights reserved.