Two methods of analysis, micellar electrokinetic capillary chromatography (
MECC) and reversed-phase high-performance liquid chromatography (RP-HPLC),
were developed for the separation and determination of selected phenolic co
mpounds (caffeic acid, catechin, catechol, chlorogenic acid, 3,4-dihydroxyp
henylacetic acid, hydroquinone, 4-methylcatechol and vanillin) of nutrition
al and pharmacological interest. Analytes were detected with UV absorption
at lambda(max) 280 and 320 nm. Although catechin and 3-4,dyhidroxyphenylace
tic acid showed peak distortion when analyzed by MECC, this technique showe
d a faster separation ability when compared to RP-HPLC. Moreover, MECC prov
ed to be a powerful tool for the repeatable and reliable quantification of
phenolic compounds providing better linearity and area calculation, while R
P-HPLC provided the better results in terms of elation time repeatability.
Finally, concentration sensitivity in MECC (101-432 mu M) were 10(3) times
higher than that of RP-HPLC (90-532 nM). However, both methods had similar
minimum detectable mass sensitivity (range: 0.31-2.15 ng) for the selected
phenolic compounds.