Electrochemical determination of paracetamol(PCT)was successfully performed using carbon paste electrodes(CPEs)modified with treated coffee husks(CHt)or cellulose powder(Ce).Scanning electron microscopy was used to ch...Electrochemical determination of paracetamol(PCT)was successfully performed using carbon paste electrodes(CPEs)modified with treated coffee husks(CHt)or cellulose powder(Ce).Scanning electron microscopy was used to characterize unmodified or modified CPEs prior to their use.The electrochemical oxidation of PCT was investigated using square wave voltammetry(SWV)and cyclic voltammetry(CV).The oxidation current density of PCT was two-fold higher with the CPE-CHt sensor and 30%higher with CPE-Ce in comparison with the unmodified CPE,and this correlated with the higher hydrophilicity of the modified electrodes.Using SWV for the electrochemical analysis of PCT,carbon paste electrode modified with raw coffee husks(CPE-CHr)showed the presence of impurities at+0.27 V/SCE,showing the interest in using pure cellulose for the present analytical application.Furthermore,CPE-Ce presented a higher real area compared to CPE-CHr,which explains the increase in the limit of saturation from 400 mg/L to 950 mg/L.The better saturation limit exhibited by CPE-Ce justifies its choice for electroanalysis of PCT in commercialized tablets.The proposed method was successfully applied in the determination of PCT in commercialized tablets(DolipraneR 500)with a recovery rate close to 100%,and no interference with the excipients contained in the tablets analyzed was observed.This novel sensor opens the way for sustainable development of electroanalytical control of drugs sold individually in developing countries.展开更多
A medium molecular weight powdered chitosan modified carbon paste electrode was used to investigate the electrochemical behaviour by cyclic voltammetry of the pharmacologically-active ingredient mangiferin (MG). An ir...A medium molecular weight powdered chitosan modified carbon paste electrode was used to investigate the electrochemical behaviour by cyclic voltammetry of the pharmacologically-active ingredient mangiferin (MG). An irreversible system was observed, with a peak at ﹢0.55 V (vs Ag/AgCl). The peak current increases about fourfold, at the modified electrode in comparison with that recorded at the chitosan free carbon paste electrode. This allowed the use of adsorptive stripping voltammetry to develop a simple and sensitive electroanalytical method for the determination of MG. The influence of key parameters was investigated, including the electrolysis potential, the preconcentration time, the pH of supporting electrolyte and MG concentration. Upon optimisation of these parameters, the electrode response was found to be directly proportional to the concentration of MG in the range from 2.06 × 10﹣6 M to 6.74 × 10﹣5 M, leading to a detection limit of 1.84 μM for 240 s preconcentration at ﹣0.1 V. A mechanism was also proposed for the electrochemical oxidation of MG.展开更多
Herein, a convenient method based on a fullerene/multiwalled carbon nanotube/Nafion modified glassy carbon electrode (fullerene/MWCNT/Naf/GCE) for the electrochemical determination of caffeine (CAF) is reported. Cycli...Herein, a convenient method based on a fullerene/multiwalled carbon nanotube/Nafion modified glassy carbon electrode (fullerene/MWCNT/Naf/GCE) for the electrochemical determination of caffeine (CAF) is reported. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used to study ionic exchange properties and conductivity the proposed electrode using [Fe(CN)6]3-/4- redox couple. Caffeine gave an irreversible oxidation peak around +1.33 V (vs. Ag/AgCl reference electrode) in HClO4 (pH 1). The linear dependence of the peak current with the square root of the scan rate showed that the electron transfer process is controlled by diffusion. After optimization of key analytical parameters involved in differential pulse voltammetry (DPV), the oxidation peak current varied linearly with CAF concentration in the range of 10 to 1000 μM. A detection limit of 7.289 × 10-8 M (S/N = 3) was found. Kinetic and chronocoulometric studies were also performed to characterize the diffusion of CAF. The developed electrode exhibited good stability and was easily regenerated. The influence of some potential interfering compounds such as dopamine, uric acid, glucose and sulfite ions on the anodic peak current of CAF was also examined. The proposed method was successfully employed in the determination of CAF in some commercial drugs.展开更多
文摘Electrochemical determination of paracetamol(PCT)was successfully performed using carbon paste electrodes(CPEs)modified with treated coffee husks(CHt)or cellulose powder(Ce).Scanning electron microscopy was used to characterize unmodified or modified CPEs prior to their use.The electrochemical oxidation of PCT was investigated using square wave voltammetry(SWV)and cyclic voltammetry(CV).The oxidation current density of PCT was two-fold higher with the CPE-CHt sensor and 30%higher with CPE-Ce in comparison with the unmodified CPE,and this correlated with the higher hydrophilicity of the modified electrodes.Using SWV for the electrochemical analysis of PCT,carbon paste electrode modified with raw coffee husks(CPE-CHr)showed the presence of impurities at+0.27 V/SCE,showing the interest in using pure cellulose for the present analytical application.Furthermore,CPE-Ce presented a higher real area compared to CPE-CHr,which explains the increase in the limit of saturation from 400 mg/L to 950 mg/L.The better saturation limit exhibited by CPE-Ce justifies its choice for electroanalysis of PCT in commercialized tablets.The proposed method was successfully applied in the determination of PCT in commercialized tablets(DolipraneR 500)with a recovery rate close to 100%,and no interference with the excipients contained in the tablets analyzed was observed.This novel sensor opens the way for sustainable development of electroanalytical control of drugs sold individually in developing countries.
文摘A medium molecular weight powdered chitosan modified carbon paste electrode was used to investigate the electrochemical behaviour by cyclic voltammetry of the pharmacologically-active ingredient mangiferin (MG). An irreversible system was observed, with a peak at ﹢0.55 V (vs Ag/AgCl). The peak current increases about fourfold, at the modified electrode in comparison with that recorded at the chitosan free carbon paste electrode. This allowed the use of adsorptive stripping voltammetry to develop a simple and sensitive electroanalytical method for the determination of MG. The influence of key parameters was investigated, including the electrolysis potential, the preconcentration time, the pH of supporting electrolyte and MG concentration. Upon optimisation of these parameters, the electrode response was found to be directly proportional to the concentration of MG in the range from 2.06 × 10﹣6 M to 6.74 × 10﹣5 M, leading to a detection limit of 1.84 μM for 240 s preconcentration at ﹣0.1 V. A mechanism was also proposed for the electrochemical oxidation of MG.
文摘Herein, a convenient method based on a fullerene/multiwalled carbon nanotube/Nafion modified glassy carbon electrode (fullerene/MWCNT/Naf/GCE) for the electrochemical determination of caffeine (CAF) is reported. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used to study ionic exchange properties and conductivity the proposed electrode using [Fe(CN)6]3-/4- redox couple. Caffeine gave an irreversible oxidation peak around +1.33 V (vs. Ag/AgCl reference electrode) in HClO4 (pH 1). The linear dependence of the peak current with the square root of the scan rate showed that the electron transfer process is controlled by diffusion. After optimization of key analytical parameters involved in differential pulse voltammetry (DPV), the oxidation peak current varied linearly with CAF concentration in the range of 10 to 1000 μM. A detection limit of 7.289 × 10-8 M (S/N = 3) was found. Kinetic and chronocoulometric studies were also performed to characterize the diffusion of CAF. The developed electrode exhibited good stability and was easily regenerated. The influence of some potential interfering compounds such as dopamine, uric acid, glucose and sulfite ions on the anodic peak current of CAF was also examined. The proposed method was successfully employed in the determination of CAF in some commercial drugs.
