F. Kusu et al., DIRECT SEPARATION AND DETERMINATION OF SYNEPHRINE ENANTIOMERS BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH ELECTROCHEMICAL DETECTION, Chemical and Pharmaceutical Bulletin, 43(7), 1995, pp. 1158-1161
High-performance Liquid chromatography (HPLC) with electrochemical det
ection using a chiral ligand-exchange column (Sumichiral OA-5000) and
a mobile aqueous phase containing 1 mM copper(II) acetate and 20 mM am
monium acetate (pH 6.4) was applied to the direct separation and deter
mination of synephrine enantiomers, The calibration curve for each ena
ntiomer showed good linearity (r=0.999) over a concentration range of
0.2-100 mu M with a detection limit of 0.2 mu M (signal-to-noise ratio
(SIN)=3). As far as reproducibility was concerned, the relative stand
ard deviation (R.S.D.) was 2.6% at 20 mu M d-synephrine and 2.4% at 20
mu M I-synephrine. The degradation and optical isomerization of I-syn
ephrine in Citrus unshiu were caused by ultraviolet (UV) light or heat
, The synephrine enantiomers in citrus plants, crude drugs and Chinese
medicines were determined by the present method.