Chiral separation and quantitation of pentazocine enantiomers in pharmaceuticals by capillary zone electrophoresis using maltodextrins

J Pharm Biomed Anal. 1999 Oct;21(1):75-81. doi: 10.1016/s0731-7085(99)00114-4.

Abstract

The chiral separation of pentazocine was achieved by capillary electrophoresis using oligosaccharides. Enantiomers were separated on 100 mM Tris/H3PO4 buffer (pH 2.5) with 5% maltodextrin as a chiral selector, and migration behavior was monitored at 200 nm. Under these conditions, (-)- and (+)-pentazocine and dextromethorphan (internal standard) migrated within 9 min, and the resolution of pentazocine enantiomers was 2.54. Linear calibration curves were obtained in the range 5-50 microg/ml(-1) for each enantiomer. The detection limit of pentazocine enantiomers was 29 pg, and the recoveries of(-)- and (+)-pentazocine were 98.9 (R.S.D., 3.4%) and 101.4% (R.S.D., 4.3%) with 10 microg/ml(-1), respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics, Opioid / isolation & purification*
  • Electrophoresis, Capillary / methods*
  • Pentazocine / isolation & purification*
  • Pharmaceutical Preparations / chemistry
  • Polysaccharides / chemistry
  • Stereoisomerism

Substances

  • Analgesics, Opioid
  • Pharmaceutical Preparations
  • Polysaccharides
  • maltodextrin
  • Pentazocine