Miriam Franco Guzman, Luis Humberto Mendoza Huizar, Carlos Andres Galan Vidal, Gabriela Roa Morales and Giaan A Alvarez Romero* Pages 294 - 304 ( 11 )
Background: Diclofenac is a widely used nonsteroidal anti-inflammatory drug. Recent studies have shown that frequent consumption of this drug in high concentrations can cause heart diseases, so strict control of diclofenac’s quantity in commercial drugs is necessary. This paper presents the development of an optimized voltammetric methodology for the quantification of diclofenac, which offers some advantages over other electrochemical and accepted methods.
Objective: Optimize with a Box-Behnken design the differential pulse voltammetry parameters towards the quantification of diclofenac in pharmaceutical samples.
Methods: Diclofenac behavior in the working electrode was evaluated by cyclic voltammetry, in order to stablish the best conditions for diclofenac’s quantification. A Box-Behnken design was then used to optimize the differential pulse voltammetry parameters and stablish the analytical behavior of the proposed methodology. Commercial tablets were prepared for analysis according to the Pharmacopeia, the DPV optimized methodology was used to quantify diclofenac in the samples, and the results were statistically compared with those obtained with the official methodology.
Results: After optimization, the analytical parameters found were: correlation coefficient of 0.998, detection limit of 0.001 μM, quantification limit of 0.0033 μM and sensitivity of 0.299 μA.μM-1. The statistical analysis showed there were no significant differences between the results obtained with the proposed methodology and those obtained with the official methodology.
Conclusion: The statistical analysis showed that the proposed methodology is as reliable as the official spectrophotometric one for the quantification of diclofenac in commercial drugs, with very competitive analytical parameters, and even better to others found with more complex electrodes.
Box-behnken optimization, carbon paste electrode, diclofenac, differential pulse voltammetry, multiwalled carbon nanotubes, pharmaceutical samples.
Universidad Autonoma del Estado de Hidalgo. Area Academica de Quimica. Carretera Pachuca-Tulancingo Km 4.5. C.P 42184. Mineral de la Reforma. Hidalgo, Universidad Autonoma del Estado de Hidalgo. Area Académica de Quimica. Carretera Pachuca-Tulancingo Km 4.5. C.P 42184. Mineral de la Reforma. Hidalgo, Universidad Autónoma del Estado de Hidalgo. Area Académica de Quimica. Carretera Pachuca-Tulancingo Km 4.5. C.P 42184. Mineral de la Reforma. Hidalgo, UAEM-UNAM. Centro Conjunto de Investigacion en Quimica Sustentable. Carretera Km. 14.5, Unidad San Cayetano, 50200, Toluca - Atlacomulco, Toluca de Lerdo, Mex., Universidad Autonoma del Estado de Hidalgo. Area Académica de Quimica. Carretera Pachuca-Tulancingo Km 4.5. C.P 42184. Mineral de la Reforma. Hidalgo