A total of ten Evodia alkaloids was separated successfully by micellar
electrokinetic capillary chromatography (MECC) and capillary zone ele
ctrophoresis (CZE). The MECC method based on SDS was applied to analyz
e three indolequinazoline alkaloids (evodiamine, rutaecarpine and carb
oxyevodiamine) and six quinolone alkaloids (1-methyl-2-nonyl-4(1H)-qui
nolone, 1-methyl-2-[(Z)-6- undecenyl] -4(1H)-quinolone, 1-methyl-2-und
ecyl-4(1H)-quinolone, evocarpine, 1-methyl-2-[(6Z,9Z)-6,9-pentadecadie
nyl]-4( 1H)-quinolone and dihydroevodiamine) in 15 min and CZE techniq
ue was used to determine the dehydroevodiamine in 5 min. Linearity ove
r one order of magnitude of concentration was generally obtained and l
imits of detection for the alkaloids were in the range of 35-47 mu g/m
l. The relative standard deviations were less than 4% (n=6). Contents
of Evodiae alkaloids in a methanol-water extract of Evodia fructus sam
ple could easily be determined by this method. The effects of pH, surf
actant concentration and organic modifier concentration of the carrier
on the migration behaviour of the solutes are discussed.