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 |
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Hauptverfasser: | , , , |
Format: | Artikel |
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. |
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ISSN: | 0731-7085 1873-264X |
DOI: | 10.1016/S0731-7085(01)00400-9 |