Electrochemical methods have been widely used for the determination of electroactive compounds due to their simplicity, sensitivity, stability, and low cost. A carbon paste electrode was modified with anthraquinone. Cyclic voltammetry (CV) was employed to study the properties of the modified electrode toward the oxidation of caffeine (CAF). Compared to the unmodified electrode, the AQMCPE showed excellent catalytic activity for the oxidation of caffeine. AQMCPE was used to determine CAF in drug samples electrochemically. SWV was used to plot the calibration curve and there was a good linear relationship between anodic peak current and CAF concentration in the range2.0×10-6-8.0×10–4 M, with the correlation coefficient of 0.998 and a detection limit of1.43×10-7 M. The application of the modified electrode for the determination of CAF in pharmaceutical formulation showed good recovery with reproducible results.
A sensitive, cost effective and selective electrochemical sensor has been developed by exploiting iron oxide nano-particles as modifier in the paste of graphite powder. Cyclic voltammetric (CV) and differential pulse voltammetric (DPV) working parameters have been standardized and used practically for the determination of chlorpyrifos (O, O-diethyl O-3, 5, 6-trichloropyridin-2-yl phosphorothioate) pesticide from its aqueous solutions. Both techniques were deployed to investigate the electro-chemical interactions between chlorpyrifos and modified carbon paste sensor along with the redox characteristics at analyte/ sensor interface. The significant enhancement in peak current signals and the improved magnitude of the redox peak potential indicated the awe-inspiring facilitation of the electron transfer process by the modifier at the sensor/ analyte interface. The difference in the redox -potential (ΔEp) and peak current ratio (Ipc/Ipa) have revealed a notable surface enhancement characteristic of the modifier that responds the higher concentration gradient of pesticide at the interface. In lower analyte's concentration range i.e. from 1.0 to 100μM, the peak current varies directly to the pesticide concentration with detection limit of 2.8 x10 -6 mol/L. The relative stability of the modified sensor is fine and the reproducibility of the results is up to 98%, even after a gap of two months. The proposed analytical method is quite successful when applied for the quantification of chlorpyrifos from its aqueous samples. The electrochemical sensing/ detection of the pesticide chlorpyrifos is confirmed by its two electrons redox behavior and the same have been explained by suitable reaction scheme as:
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