Abstract

Uric acid (UA) levels in biological fluids are an important diagnostic and prognostic biomarker for various metabolic disorders. Therefore, a convenient, facile, one-step electroreduction method to develop Fe nanostructured (FeNS) interfaces for highly sensitive electrochemical detection of UA. The synthesis process was thoroughly investigated at various deposition potentials, pH of the electrochemical bath solutions, and growth durations to attain excellent electrochemical response towards UA detection. The morphology and elemental composition of the FeNS/MWCNT were analyzed using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDXS) techniques. We observed uniform deposition of FeNSs with sizes ranging from 100 − 120 nm on tubular nanostructures. The multiwalled carbon nanotubes supported Fe nanostructured interfaces (FeNS/MWCNT) generated at a potential of –1.1 V demonstrated excellent electrochemical response towards UA with a wide linear detection range of 5 to 500 µM with a sensitivity of 6.5605 µA µM−1 cm−2 and low detection limit of 3.26 µM. The excellent electrochemical response was attributed to the synergistic effect of MWCNTs, which facilitated FeNSs growth, leading to increased active sites for electrocatalysis and sensitive detection of UA. The convenience of the synthesis process, tunable electrochemical response, and reliability of the detection process make FeNS interfaces a potential option for developing electrochemical UA sensors.

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