Electroanalytical Determination of Promethazine Hydrochloride in Pharmaceutical Formulations on Highly Boron-Doped Diamond Electrodes Using Square-Wave Adsorptive Voltammetry

• Published in: Electroanalysis (New York, N.Y.) Vol. 20; no. 18; pp. 2031 - 2039
• Main Authors: Ribeiro, Francisco Wirley P., Cardoso, Amanda S., Portela, Rafael R., Lima, Janete E. S., Machado, Sergio A. S., de Lima-Neto, Pedro, De Souza, Djenaine, Correia, Adriana N.
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY-VCH Verlag 01-09-2008; WILEY‐VCH Verlag
• Subjects: Highly boron-doped diamond electrode; Pharmaceutical formulations; Promethazine hydrochloride; Square-wave adsorptive voltammetry
• ISSN: 1040-0397; 1521-4109
• DOI: 10.1002/elan.200804286

The electrochemical oxidation of promethazine hydrochloride was made on highly boron‐doped diamond electrodes. Cyclic voltammetry experiments showed that the oxidation mechanisms involved the formation of an adsorbed product that is more readily oxidized, producing a new peak with lower potential values whose intensity can be increased by applying the accumulation potential for given times. The parameters were optimized and the highest current intensities were obtained by applying +0.78 V for 30 seconds. The square‐wave adsorptive voltammetry results obtained in BR buffer showed two well‐defined peaks, dependent on the pH and on the voltammetric parameters. The best responses were obtained at pH 4.0, frequency of 50 s−1, step of 2 mV, and amplitude of 50 mV. Under these conditions, linear responses were obtained for concentrations from 5.96×10−7 to 4.76×10−6 mol L−1, and calculated detection limits of 2.66×10−8 mol L−1 (8.51 μg L−1) for peak 1 and of 4.61×10−8 mol L−1 (14.77 μg L−1) for peak 2. The precision and accuracy were evaluated by repeatability and reproducibility experiments, which yielded values of less than 5.00% for both voltammetric peaks. The applicability of this procedure was tested on commercial formulations of promethazine hydrochloride by observing the stability, specificity, recovery and precision of the procedure in complex samples. All results obtained were compared to recommended procedure by British Pharmacopeia. The voltammetric results indicate that the proposed procedure is stable and sensitive, with good reproducibility even when the accumulation steps involve short times. It is therefore very suitable for the development of the electroanalytical procedure, providing adequate sensitivity and a reliable method.