Abstract
An ex situ bismuth film electrode (BiFE) was used for the electrochemical study of the hormone progesterone. Two peaks were observed by cyclic voltammetry, at −1.68V and −1.47V, respectively, associated with the reduction and oxidation reactions of progesterone in 0.1molL−1 Britton–Robinson solution at pH 12.0, in agreement with a quasireversible electrode process. In relation to the mechanism, an adsorption-controlled reaction rate with one electron involved in the electrochemical step was observed. Square-wave adsorptive stripping voltammetry was used for the analytical procedures after accumulation of the progesterone for 60s at −1.0V. A peak current at −1.63V related to the reduction of progesterone was obtained, which increased linearly with the hormone concentration in the range of 0.40–7.90μmolL−1 (R2=0.9983). The limit of detection attained was 0.18μmolL−1. The method was applied in the determination of progesterone in four pharmaceutical samples with satisfactory results being obtained compared with a spectrophotometric method.
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