Uric acid (UA) has been under intensive investigation by electrochemis
ts owing to its important role as a metabolite in biological fluids. O
ne of the major problems in biological determinations of uric acid com
es from electrochemical interferences such as ascorbic acid (AA), whic
h has a similar oxidation potential, E-1/2 approximate to 200 mV versu
s SCE, at graphite electrodes, and is present at high concentrations i
n biological systems. UA undergoes a 2 H+, 2 e(-) oxidation in aqueous
buffers, The oxidation product, a diimine, is an unstable intermediat
e with a half-life of less than 22 ms. A follow-up hydration reaction
converts the diimine to an imine alcohol. Results of previous work sho
w that UA weakly adsorbs and undergoes a fast electron transfer reacti
on, k(s) = 54 s(-1), at carbon fiber electrodes. These characteristics
make UA an excellent candidate for fast scan voltammetric (FSV) deter
minations. This paper presents the results of FSV at bare carbon fiber
electrodes. The results show good selectivity and sensitivity in the
determination of low concentrations of UA in the presence of high conc
entrations of AA, By increasing the scan rate above 500 V s(-1), volta
mmograms of UA in the presence of AA can be resolved because of the ki
netic differences in the response of the two anions, without the need
for a permselective film on the electrode. Results are also presented
that demonstrate an effective way to reach a stable background current
at bare carbon fiber electrodes, which is required in FSV because the
signal from the analyte is smaller than the electrochemical signal fr
om the background current. Signal-to-noise ratios at bare carbon fiber
electrodes in FSV are improved, because the high temporal resolution
in fast scan methods allows the acquisition of a large number of scans
that can be signal averaged in a short period of time. In addition, l
arge signals can be measured because the voltammetric peak current inc
reases with increase in scan rate.