Enantiomeric separation of antimalarial drugs by capillary electrophoresis using neutral and negatively charged cyclodextrins

J Pharm Biomed Anal. 2011 Feb 20;54(3):475-81. doi: 10.1016/j.jpba.2010.09.020. Epub 2010 Sep 19.

Abstract

Capillary electrophoresis (CE) methods for chiral resolution of five antimalarial drugs (primaquine, tafenoquine, mefloquine, chloroquine and quinacrine) were developed by using a wide selection of neutral and anionic cyclodextrin (CD) derivatives. The use of sulfobutyl-β-CD and carboxymethyl-β-CD (CMBCD) resulted in good resolution of quinacrine and tafenoquine, respectively. New results are presented for resolutions of chloroquine and mefloquine. Application of carboxyalkyl- and sulfobutyl-CD derivatives provided improved resolution for primaquine. The impurity in primaquine sample detected by CE was identified as quinocide by MS and NMR. CMBCD provided not only the best separation of primaquine from quinocide but also the simultaneous complete resolution of both compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminoquinolines / analysis*
  • Anions
  • Antimalarials / analysis*
  • Chloroquine / analysis*
  • Cyclodextrins / chemistry
  • Electrophoresis, Capillary
  • Humans
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Mefloquine / analysis*
  • Primaquine / analysis*
  • Stereoisomerism
  • beta-Cyclodextrins / chemistry*

Substances

  • Aminoquinolines
  • Anions
  • Antimalarials
  • Cyclodextrins
  • beta-Cyclodextrins
  • carboxymethyl-beta-cyclodextrin
  • tafenoquine
  • Chloroquine
  • quinocide
  • Primaquine
  • Mefloquine