First Electrochemical Study of a Potent Antifungal Drug Caspofungin: Application To Its Enhanced Voltammetric Sensing Based on the Performance of Boron-Doped Diamond Electrode in Ctab-Mediated Measurements
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Date
2022
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Elsevier Science Sa
Abstract
This present study describes the first electrochemical investigation of caspofungin, which is a semisynthetic echinocandin class of antifungal drug. For this purpose, an electrochemically pretreated (anodically and subsequently cathodically) boron-doped diamond (BDD) electrode was used. The cyclic voltammetric scans showed a single oxidation step that is irreversible and controlled by a dual mechanism of adsorption and diffusion. For the optimization of experimental conditions, the influence of the electrode pretreatment, pH of the supporting electrolyte, concentration of cationic surfactant cetyltrimethylammonium bromide (CTAB), accumulation variables, and instrumental parameters was examined on the current response of caspofungin. The improved sensitivity of the voltammetric measurements was observed due to the synergistic effect of CTAB on the adsorption capacity of BDD electrode in alkaline pH conditions. Employing square-wave adsorptive stripping voltammetry (using open-circuit accumulation for 60 s), the oxidation signal at around +0.45 V allowed to the determination of caspofungin in Britton-Robinson buffer at pH 11.0 containing 1 x 10-4 M CTAB. The process could be used in the concentration range from 2.06 x 10-7 to 1.03 x 10-5 M (from 0.25 to 12.5 mu g mL-1 as acetate salt) with a detection limit of 5.27 x 10-8 M (0.064 mu g mL-1 as acetate salt). A technique developed here was used successfully to determine caspofungin concentration in commercial parenteral dosage formulations.
Description
Yardim, Yavuz/0000-0002-9587-096X; Ali, Hoshyar/0000-0002-9138-485X; Barzani, Hemn Abdulazeez Hakeem/0000-0002-1875-7760
Keywords
Caspofungin, Boron-Doped Diamond Electrode, Cationic Surfactant, Square-Wave Adsorptive Stripping Voltammetry, Pharmaceutical Formulation
Turkish CoHE Thesis Center URL
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Q2
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Q2
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Volume
125