A highly sensitive method is described for the determination of oxamni
quine in its pure form and in capsules. The proposed method depends up
on the polarographic activity of oxamniquine in Britton-Robinson buffe
r, whereby a well-defined cathodic wave, followed by a more negative i
ll-defined one, was produced over the whole pH range. The first wave w
as characterized as being irreversible and diffusion-controlled with l
imited absorption properties. The current-concentration relationship w
as found to be rectilinear over the ranges 1 x 10(-5) to 5 x 10(-4) an
d 1 10(-6) to 5 x 10(-4) M in the direct current (DCT) and differentia
l pulse polarography (DPP) modes, respectively, with a minimum detecta
bility of 1 x 10(-7) M. The number of electrons involved in the reduct
ion process was established through coulometric measurement at an appl
ied potential. The mechanism of the electrode reaction was verified an
d confirmed through chemical reactions of the electrolyzed solution. T
he proposed method was successfully applied to the determination of ox
amniquine in capsules, and the results obtained were in accordance wit
h those found using the United States Pharmacopeia (USP) XXII method.