<p>Electrochemical sensors have emerged as a valuable tool for detecting selective and sensitive antioxidants. Chromium oxide (Cr<sub>2</sub>O<sub>3</sub>) nanoparticles have shown great potential as modifiers for carbon paste electrodes (CPEs), owing to their superior conductivity and favorable electrochemical characteristics. Cr<sub>2</sub>O<sub>3</sub> nanoparticles were synthesized by the combustion method using chromium (III) nitrate as oxidizer and glycine as a fuel, with the reaction carried out at 350&#xa0;°C. Their microstructural features are analyzed through techniques of FESEM and XRD. The electroanalytical performance of a modified electrode (PGly/Cr<sub>2</sub>O<sub>3</sub>/CPE) for antioxidant Rutin (RU) detection was investigated in phosphate buffer solution (PBS, pH 6.6) by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and differential pulse voltammetry (DPV). The diffusion-controlled nature of the electrochemical process is confirmed through sweep rate variation studies. Differential pulse voltammetry (DPV) analysis demonstrated a low detection limit of 0.21&#xa0;μM for RU. The modified electrode exhibited outstanding selectivity for interfering ions and achieved an accuracy of 99.83- 111.26% in real sample analysis. The PGly/Cr<sub>2</sub>O<sub>3</sub>/CPE sensor demonstrated outstanding catalytic activity, along with selectivity, sensitivity, reproducibility, repeatability, and stability for the detection of Rutin (RU).</p> Graphical Abstract <p></p>

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Chromium oxide/poly (glycine) modified electrode sensor for rutin: a voltammetric method

  • Chethan M. Kuskur,
  • Ramesh S. Bhat,
  • B. E. Kumara Swamy

摘要

Electrochemical sensors have emerged as a valuable tool for detecting selective and sensitive antioxidants. Chromium oxide (Cr2O3) nanoparticles have shown great potential as modifiers for carbon paste electrodes (CPEs), owing to their superior conductivity and favorable electrochemical characteristics. Cr2O3 nanoparticles were synthesized by the combustion method using chromium (III) nitrate as oxidizer and glycine as a fuel, with the reaction carried out at 350 °C. Their microstructural features are analyzed through techniques of FESEM and XRD. The electroanalytical performance of a modified electrode (PGly/Cr2O3/CPE) for antioxidant Rutin (RU) detection was investigated in phosphate buffer solution (PBS, pH 6.6) by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and differential pulse voltammetry (DPV). The diffusion-controlled nature of the electrochemical process is confirmed through sweep rate variation studies. Differential pulse voltammetry (DPV) analysis demonstrated a low detection limit of 0.21 μM for RU. The modified electrode exhibited outstanding selectivity for interfering ions and achieved an accuracy of 99.83- 111.26% in real sample analysis. The PGly/Cr2O3/CPE sensor demonstrated outstanding catalytic activity, along with selectivity, sensitivity, reproducibility, repeatability, and stability for the detection of Rutin (RU).

Graphical Abstract