An enantioselective assay for (±)-modafinil

Enantiomers of modafinil, (diphenylmethyl)sulphinyl-2-acetamide, were separated by an amylose tris[( S)-1-phenylethylcarbamate] chiral stationary phase, using acetonitrile: water (25:75 v/v) as mobile phase, with excellent selectivity ( α=1.4) and resolution factors ( R s =1.5). The assay involved a...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2001-08, Vol.26 (1), p.123-130
Hauptverfasser: Cass, Quezia B, Kohn, Cristiane K, Calafatti, Silvana A, Aboul-Enein, Hassan Y
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Sprache:eng
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Zusammenfassung:Enantiomers of modafinil, (diphenylmethyl)sulphinyl-2-acetamide, were separated by an amylose tris[( S)-1-phenylethylcarbamate] chiral stationary phase, using acetonitrile: water (25:75 v/v) as mobile phase, with excellent selectivity ( α=1.4) and resolution factors ( R s =1.5). The assay involved a solid-phase extraction of the enantiomers of modafinil from plasma using a C 18 Cartridge. A good linear relationship was obtained in the concentration of 0.15–3 μg ml −1 for each enantiomer. The method developed is sufficiently accurate and precise to be used for clinical samples and has a good selectivity with the two main circulating metabolites: the (diphenylmethyl)sulphinyl-2-acetic acid and (diphenylmethyl)sulphonyl-2-acetamide. The use of a polysaccharide-based column on multimodal elution was explored in developing the method.
ISSN:0731-7085
1873-264X
DOI:10.1016/S0731-7085(01)00400-9