Spectrophotometric methods based on charge transfer complexation reaction for the determination of some antifungal drugs in pure and dosage forms

• Main Authors: A. A. Gouda, R. El Sheikh, A. S. Amin, S. H. Ibrahim
• Format: Article
• Language: English
• Published: Chemical Society of Ethiopia 2017-01-01
• Series: Bulletin of the Chemical Society of Ethiopia
• Subjects: Fluconazole; Sertaconazole nitrate; Miconazole nitrate; Charge transfer complexes; Spectrophotometry; Pharmaceutical formulations
• Online Access: https://www.ajol.info/index.php/bcse/article/view/149945
• ISSN: 1011-3924; 1011-3924

Charge transfer complexes of some antifungal drugs fluconazole (FLU), sertaconazole nitrate (SER) and miconazole nitrate (MCO) as electron donor with the σ-acceptor iodine (I2) and 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ), p-chloranilic acid (p-CLA) and 7,7,8,8-tetracyanoquinodimethane (TCNQ) as π-acceptors in acetonitrile were investigated. The formation of the colored charge-transfer complexes were utilized in the development of simple, rapid and accurate spectrophotometric methods for the analysis of the cited drugs in pure forms and pharmaceutical formulations at 365 nm for MCO and SER using I2 method, at 460 nm for FLU and SER using DDQ method, at 535 and 530 nm for FLU and SER, respectively, using p-CLA method and at 842 nm for MCO and SER using TCNQ method. The optimum experimental conditions have been studied carefully and optimized. Beer’s law was obeyed over the concentration ranges of 2.0–28, 10–240 and 2.0–160 µg mL−1 for MCO, FLU and SER, respectively, with good correlation coefficients (0.9996–0.9999). Molar absorpitivity, Sandell sensitivity, relative standard deviation, limit of detection and quantification were calculated. The obtained data refer to high accuracy and precision of the proposed method. The obtained results were confirmed by inter and intra-day accuracy and precision with percent recovery of 99.1–100%, 99.3–101% and 99.1–101% for MCO, FLU and SER, respectively. These data were compared with those obtained using official methods for the determination of the cited drugs. The proposed methods were applied successfully for simultaneous determination of the cited drugs in their pharmaceutical formulations with good accuracy and precision and without interferences from common additives.