G. Boonen et al., CONTRIBUTION TO THE QUANTITATIVE AND ENANTIOSELECTIVE DETERMINATION OF KAVAPYRONES BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY ON CHIRASPHER NT MATERIAL, Journal of chromatography B. Biomedical sciences and applications, 702(1-2), 1997, pp. 240-244
Citations number
8
Journal title
Journal of chromatography B. Biomedical sciences and applications
A simultaneous HPLC separation of the enantiomers of kavain, dihydroka
vain, methysticin and dihydromethysticin, as well as the achiral dieno
lides yangonin and desmethoxyyangonin was carried out on a ChiraSpher
NT column. For quantitative determinations, calibration curves with co
rrelation coefficients between 0.9982 and 0.9996 were established for
the genuine kavapyrones. Detection limits between 0.25 mu g and 0.5 mu
g per injection were measured at 240 nm. The defined scopes of work c
orresponded with the different kavapyrone amounts, depending on growth
factors of distinct plant locations The precision of the method was v
erified by analysing a phytopharmacon with a nominal value of 40 mg ka
vapyrones per tablet. The evaluation revealed 39.62 mg per tablet by t
he sum of single calculated kavapyrones. Relative standard deviations
between 1.06% and 2.39% were found for the compounds under investigati
on. The accuracy of the method was proved by a recovery of 99.7%. To s
implify the determination of the total kavapyrone amount, response fac
tors and correlation factors for (+)-dihydrokavain, (+)-methysticin, (
+)-dihydromethysticin, yangonin and desmethoxyyangonin were calculated
relative to (+)-kavain. (C) 1997 Elsevier Science B.V.