Chlorpromazine hydrochloride (CPH) (3-(2-chloro-phenothiazine-10-yl)-propyl] dimethylamine hydrochloride) has been the subject of a large number of studies employing a broad spectrum of oxidants, and chosen to examine the course of electron transfer reactions. We report on a method to determine the antioxidant activity of some food and medicinal plants using the oxidation of CPH by chromium(VI) to form a stable CPH radical in the 1:1 orthophosphoric acid-ethyl alcohol (OPA-EtOH) medium. The pink color of the control solution was measured at λmax of 530 nm. Nine standard antioxidants have been studied by this method, along with the 2,2-diphenyl-1-picrylhydrazyl (DPPH) method. The EC50, TEC50, antioxidant efficacy and the stoichiometric values for antioxidants have been evaluated. The radical scavenging activity expressed as EC50 ranged from 9.2 μg/mL in Camellia sinensis to 448.18 μg/mL in Cuminum cyminum. The application of a simple and versatile antioxidant capacity assay for dietary polyphenols and medicinal plant extracts, which are commonly used in Ayurveda opens its relevance in the field of antioxidant analysis.
A facile, and novel construction strategy invented on electrochemical procedures for the assemblage of zinc oxide nanoparticles (ZnO NPs) with a multiwalled carbon nanotube modified carbon paste electrode (ZnO-MWCNTMCPE) to ascertain the fluoroquinolone drug-Moxifloxacin (MOX). The ZnO-MWCNTMCPE can significantly improve the electron transfer process and lessen the impedance of the surface of the electrode. Besides, the oxidation of MOX has remarkably enhanced on the modified electrode. Under the optimal experimental conditions, the empirical results exhibited that the oxidation peak current was linearly proportional to the concentration of MOX in the range of 1.0 × 10 À 7 to 2.4 × 10 À 6 mol L À 1 with a detection limit of 0.452 × 10 À 7 mol L À 1. To analyze the practicality of the MOX determination technique in real samples, the intended sensor manipulated for the adjudication of MOX in human urine specimens, and the results authenticated the explore of MOX with the highest accuracy. Further, the proposed sensor system exercised for the simultaneous evaluation of paracetamol (ACOP) and MOX, the DPV technique unveiled the well-separated peaks among ACOP (0.188 mV) and MOX (0.814 mV) with a peak separation (ΔE) of 626 mV in real samples. Therefore, the suggested system could sense and discover the MOX in the biological systems.
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