Determination of rutin and L-ascorbic acid in pharmaceutical preparations and fruit juices by capillary zone electrophoresis with electrochemical detection
G. Chen et al., Determination of rutin and L-ascorbic acid in pharmaceutical preparations and fruit juices by capillary zone electrophoresis with electrochemical detection, CHEM J CH U, 21(9), 2000, pp. 1364-1368
A simultaneous determination of rutin(RT) and L-ascorbic acid(Vc) in pharma
ceutical preparations and fruit juices by capillary zone electrophoresis wi
th electrochemical detection(CE-ED) was reported, The effects of potential
of working electrode, concentration and pH of the running buffer, separatio
n voltage and injection time on the CE-ED determination were investigated a
nd discussed. RT and Vc could be well separated in a 25 mmol/L borax-50 mmo
l/L NaH2PO4 buffer(pH 8.0) within 12 min. A 300 mum diameter carbon disc el
ectrode was used as the working electrode positioned carefully opposite the
outlet of the capillary in a wall-jet configuration at potential of 1.0 V
(vs. SCE), There are excellent linearity between peak current and concentra
tion of analytes in the concentration range of 1.0 x 10(-6)-2.5 x 10(-4) mo
l/L for RT and 5.0 x 10(-6)-2.5 x 10(-3) mol/L for Vc with the detection li
mits (S/N = 3) of 8.0 x 10(-7) and 3.3 x 10(-6) mol/L for RT and Vc, respec
tively. Relative standard deviations (RSD) of the peak currents of RT and V
c were 2.85% (RT) and 1.65% (Vc) based on 9 determinations of the same samp
le containing 5.0 x 10(-5) mol/L RT and 2.5 x 10(-4) mol/L Vc. Recoveries o
f 97.94% for RT and 99.68% for Vc were obtained based on 5 determinations.