Abstract
The anodic oxidation of naproxen has been carried out on a platinum electrode using cyclic, linear sweep and differential pulse voltammetry (DPV). Naproxen exhibited a single well-defined and irreversible peak in acetonitrile/0.1 M LiClO 4 with a peak potential at 1146 mV versus Ag/AgCl. This allowed the development of a simple, selective and sensitive differential pulse voltammetric method for the determination of naproxen in pharmaceuticals. The calibration plot was linear ( R 2=0.998) over the range 1–25 μg ml −1. The limit of detection (3 σ/ m) was 0.24 μg ml −1 and the relative standard deviation of the measurements was 1.2% ( n=6). Well-defined peaks for two related compounds to naproxen (2-methoxy-6-ethylnaphthalene (MEN) and 2-acetyl-6-methoxynaphthalene (AMN)) were detected, respectively, at 1096 and 1316 mV versus Ag/AgCl and no interference was measured during the determination of naproxen. The limits of detection of MEN and AMN were found to be respectively 0.28 and 0.21 μg ml −1. The method was successfully applied to the determination of naproxen in commercial tablets and showed a good sensitivity and accuracy with mean recoveries between 99.8 and 101.2%.
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