Al. Bordes et al., REDOX LABELING OF 2 ANTIEPILEPTIC DRUGS WITH METALLOCENES AND THEIR SIMULTANEOUS DETECTION BY A NAFION-MODIFIED ELECTRODE, Applied organometallic chemistry, 12(1), 1998, pp. 59-65
Two different cationic redox labels, i.e. a ferroceneammonium ion and
a cobaltocenium ion, mere covalently attached to two anti-epileptics,
phenytoin and phenobarbital, respectively, The two labeled drugs posse
ss distinct standard redox potentials of 0.39 V for the phenytoin deri
vative and -0.92 V for phenobarbital derivative (vs Ag/AgCl, Cl- 0.05
M) at a carbon paste electrode, After preconcentration in a polyanioni
c Nafion-loaded carbon paste electrode the positively charged labeled
phenytoin and phenobarbital derivatives could be simultaneously detect
ed in concentration ranges which were relevant to the therapeutic rang
es of the antiepileptics, with a view to a future dual-analyte immunoa
ssay, Square-wave voltammetry permitted detection limits of 5 x 10(-8)
M (for the phenytoin derivative) and 2.5 x 10-(8) M (for the phenobar
bital derivative) for non-simultaneous detection. (C) 1998 John Whey &
Sons, Ltd.