`Nitric oxide (NO) is quickly oxidized to nitrite and nitrate in aqueo
us and biological solutions, making direct measurement of this labile
compound difficult, Quantitative analysis of nitrite and nitrate has b
een used extensively as an indirect measurement of endogenous producti
on of NO in biological systems, The colorimetric reaction of nitrite w
ith Griess reagent is probably the most commonly used technique for an
alysis of total nitrite and nitrate, This technique is useful for the
measurement of basal NO production with a lower detection limit of 25
nM, yet is not suitable for kinetic studies and suffers from interfere
nce from free thiols, proteins and other plasma constituents(1,2). Fur
thermore, only a limited number of samples can be analysed at a time o
n a continuous basis because the development of the colour reaction ma
y take 5 min or more. Here we report an electrochemical method of dete
ction of nitrite and nitrate, which has several advantages over photom
etric analysis.