A sensitive (10.0 ng/ml) and stereoselective HPLC method for analysis
of S(-)- and R(+)-dipraferone in human plasma has been developed. The
assay is based on derivatization with homochiral R(-)-1-(1-naphthyl)et
hyl isocyanate to give the diastereomeric derivates and their separati
on and quantitation using HPLC with UV-detection (220 nm). Details of
this stereoselective assay procedure which has already been applied to
the multisample analyses from a human pharmacokinetic study are descr
ibed. The data obtained indicated that the stereoselective disposition
of diprafenone enantiomers is quite different from their structural a
nd pharmacological analog propafenone.