The use of a highly sulfated cyclodextrin for the simultaneous chiral separation of amphetamine-type stimulants by capillary electrophoresis
- 1 May 2002
- journal article
- research article
- Published by Wiley in Electrophoresis
- Vol. 23 (9) , 1328-1334
- https://doi.org/10.1002/1522-2683(200205)23:9<1328::aid-elps1328>3.0.co;2-z
Abstract
We investigated the simultaneous chiral separation of nine amphetamine type stimulants (dl-norephedrine, dl-norpseudoephedrine, dl-ephedrine, dl-pseudoephedrine, dl-amphetamine, dl-methamphetamine, dl-methylenedioxyamphetamine (MDA), dl-methylenedioxymethamphetamine (MDMA), and dl-methylenedioxyethylamphetamine (MDEA)) by capillary electrophoresis using highly sulfated γ-cyclodextrin (SU(XIII)-γ-CD) as a chiral selector. Three different approaches using SU(XIII)-γ-CD with 50 mM phosphate background electrolyte were designed; (I) high CD concentration (10 mM SU(XIII)-γ-CD) at neutral pH (pH 7.0) in the normal polarity mode, (II) low CD concentration (1.0 mM) at low pH (pH 2.6) in the normal polarity mode and (III) high CD concentration at low pH (pH 2.6) in the reversed-polarity mode. In mode (II), the effects of adding three neutral CDs (β-CD, dimethyl-β-CD and hydroxypropyl-β-CD) were also investigated. The best separation was obtained after optimizing mode (III) as follows: run buffer of 10 mM SU(XIII)-γ-CD with 50 mM phosphate background electrolyte at pH 2.6, applied voltage of –12 kV and capillary temperature of 15°C.Keywords
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