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

Citation
T. Watanabe et al., Chiral separation and quantitation of pentazocine enantiomers in pharmaceuticals by capillary zone electrophoresis using maltodextrins, J PHARM B, 21(1), 1999, pp. 75-81
Citations number
23
Categorie Soggetti
Chemistry & Analysis
Journal title
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
ISSN journal
07317085 → ACNP
Volume
21
Issue
1
Year of publication
1999
Pages
75 - 81
Database
ISI
SICI code
0731-7085(199910)21:1<75:CSAQOP>2.0.ZU;2-I
Abstract
The chiral separation of pentazocine was achieved by capillary electrophore sis using oligosaccharides. Enantiomers were separated on 100 mM Tris/H3PO4 buffer (pH 2.5) with 5% maltodextrin as a chiral selector, and migration b ehavior was monitored at 200 nm. Under these conditions, (-)- and (+)-penta zocine and dextromethorphan (internal standard) migrated within 9 min, and the resolution of pentazocine enantiomers was 2.54. Linear calibration curv es were obtained in the range 5-50 mu g ml(-1) for each enantiomer. The det ection 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%) wit h 10 mu g ml(-1), respectively. (C) 1999 Elsevier Science B.V. All rights r eserved.