Me. Laethem et al., CHIRAL HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF OXPRENOLOL IN PLASMA, Journal of chromatography. Biomedical applications, 621(2), 1993, pp. 225-229
A sensitive, stereospecific high-performance liquid chromatographic as
say for oxprenolol enantiomers in rat plasma was developed, using a ch
iral derivatization agent. Racemic oxprenolol and the internal standar
d (racemic propranolol) are extracted with dichloromethane after alkal
inization of the plasma. Quantitation of R(+)- and S(-)-oxprenolol is
based on derivatization with the chiral agent S(-)-1-(1-naphthyl)-ethy
l isocyanate, followed by chromatographic separation on a C-18 reverse
d-phase column, with fluorometric detection (excitation at 226 nm, emi
ssion at 333 nm). The assay is reproducible as judged by a coefficient
of variation of less than 17.5% for bath enantiomers at all concentra
tions used. Preliminary experiments in the rat demonstrate that the me
thod is sufficiently sensitive for pharmacokinetic studies in that spe
cies.