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Improved enantioselective method for the determination of the enantiomers of reboxetine in plasma by solid-phase extraction, chiral derivatization, and column-switching high-performance liquid chromatography with fluorescence detection


Improved enantioselective method for the determination of the enantiomers of reboxetine in plasma by solid-phase extraction, chiral derivatization, and column-switching high-performance liquid chromatography with fluorescence detection



Journal of Chromatography. a 828(1-2): 167-176



ISSN/ISBN: 0021-9673

PMID: 9916303

DOI: 10.1016/s0021-9673(98)00664-5

A rapid enantioselective method is described for the quantitation of the reboxetine (R,R)- and (S,S)-enantiomers in plasma utilizing solid-phase extraction, derivatization, normal-phase high-performance liquid chromatography, and fluorescence detection. Plasma samples (0.1 ml) with added internal standard were applied to activated solid-phase extraction discs containing a nonpolar/strong cation mixed-phase, washed, eluted, evaporated to dryness, and derivatized for 5 min with (+)-1-(9-fluorenyl)ethyl chloroformate. After termination of the derivatization reaction, the samples were analyzed by isocratic normal-phase HPLC using a silica column and ethanol-heptane (1:124, v/v) as mobile phase. The derivatized reboxetine peak was column-switched onto cyano and Chiralcel OD-H columns in series using ethanol-heptane (1:49, v/v) as mobile phase to resolve the diastereomeric derivatives of the enantiomers and separate interferences. The column effluent was monitored with fluorescence detection at 260/315 nm. The range of quantitation of each enantiomer was 2-2000 ng/ml. One sample was injected every 18 min.

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Accession: 046350502

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