Journal
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
Volume 32, Issue 5, Pages 5602-5613Publisher
SPRINGER
DOI: 10.1007/s10854-021-05282-1
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A method for simultaneous electrochemical determination of dopamine, uric acid, and guanine was reported, utilizing the binding of curcumin on the electrode surface to enhance sensor performance. The modified electrode showed a large surface area, long stability, good adaptability, anti-interference capability, and significant reproducibility, with high electrocatalytic activity towards analyte oxidation, particularly for dopamine.
The binding of curcumin on the surface of AgNPs-sodium dodecyl sulfate (SDS)-multi-walled carbon nanotubes-glassy carbon electrode (CM/AgNPs/SDS/MWCNTs) was reported for simultaneous electrochemical determination of dopamine (DA), uric acid (UA) and guanine (GU). Morphological properties of modified electrodes surfaces were characterized using different voltammetry methods. The microscopic area of the modified electrode was obtained 0.139 cm(-2) using chronoamperometry analysis. The scanning electron microscope (SEM), XRD, and TEM were used to monitor the sensor fabrication. The zeta potential results showed that SDS dispersed the pure AgNPs, and the AgNPs were significantly stabilized. Also, the results showed that the constructed CM-functionalized nanocomposite create a large surface area, long stability, good adaptability, anti-interference capability, and significant reproducibility. The electrochemical results confirmed that the fabricated nanocomposite has a high electrocatalytic activity toward the oxidation of analytes especially for DA (vs. Ag/AgCl). While the above results hold true for DA, UA, and guanine GU determination, there was no comparable electrochemical peak for ascorbic acid (AA). The calibration curves were linear in the range of 12.0-200.0, 16.0-400.0, and 18-650.0 mu mol L-1 for DA, GU, and UA, respectively. The detection limit values were 0.14 mu mol L-1 for DA, 0.19 mu mol L-1 for GU, and 0.38 mu molL(-1) for UA. The prepared electrode was applied successfully to the simultaneous determination of analytes in blood, serum, urine, and dopadic ampoule samples.
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