DSpace

King Saud University Repository >
King Saud University >
COLLEGES >
Health Colleges >
College of Pharmacy >
College of Pharmacy >

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/17240

Title: Resolution of Nomifensine Enantiomers on Selected Achiral and Chiral Stationary Phases Using High Performance Liquid Chromatography
Authors: Mohamed M Hefnawy
James T Stewart
Issue Date: 1999
Publisher: LANL
Abstract: The separation of the enantiomers of nomifensine maleate, a psychotropic drug, were investigated using achiral and chiral stationary phases Three stationary phases were studied for their ability to separate the enantiomers: reversed phase cyanopropyl with a chiral mobile phase additive; inclusion (cellulose tris 3,5-dimethylphenyl carbonate (chiracel OD); and brush/pirkle type (S-tert-leucine, (R)-1-(α-naphthyl) ethylamine (Sumichiral OA-4700). Changes in mobile phase composition were studied to determine the effect of solvents on the separation of the enantiomers. Baseline separations were achieved for nomifensine enantiomers under isocratic conditions on the cyanopropyl column with 90:10 v/v 0.1% triethylamine-acetonitrile pH 4.0 (adjusted by trifluoroacetic acid) containing 10 mM β-cyclodextrin, on a Chiracel OD column using hexane-absolute methanol (96:4 v/v), and on a Sumichiral OA-4700.column using hexane-dichloroethane-absolute ethanol-trifluoroacetic acid (100:12.5:8.5:0.1v/v/v/v). The flow rates were 0.8 mL/min with detection at 292 nm. DOI: 10.1080/00032719908542605
URI: http://hdl.handle.net/123456789/17240
Appears in Collections:College of Pharmacy

Files in This Item:

File Description SizeFormat
14.doc55 kBMicrosoft WordView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

DSpace Software Copyright © 2002-2007 MIT and Hewlett-Packard - Feedback