The electrochemical oxidation of catechol to ortho quinone at a glassy carb
on electrode in the presence of cysteine is shown to lead to the deposition
of a quinone-cysteine adduct at the electrode surface. Square wave voltamm
etry is shown to enable voltammetric resolution of unreacted orthoquinone a
nd the accumulated adduct species such that quantification of both species
is possible over a range of pH 2-pH 6. The reaction is shown to be selectiv
e towards cysteine with little interference from cystine, homocysteine or g
lutathione. The foundations of a detection protocol are reported with the s
ensitivity shown to be capable of attenuation through the facile manipulati
on of the number of electro-initiated derivatisation scans. The application
of six consecutive derivatisation scans is shown to provide a linear range
of 2-20 muM cysteine that is well within the region required for physiolog
ical monitoring.