A homogeneous spectrophotometric EMIT immunoassay for the measurement
of digoxin has been converted to an amperometric immunoassay format ca
pable of analysing digoxin in diluted serum. NADH produced by glucose-
6-phosphate dehydrogenase (G6PDH) labelled digoxin was detected ampero
metrically by its rapid, efficient oxidation at platinized activated c
arbon electrodes (PACE) poised at +150 mV vs Ag/AgCl. The new amperome
tric procedure resulted in a simplified assay protocol with a decrease
d overall assay time, enhanced NADH detection and minimal sample pretr
eatment.