4.7 Article

Single-atom electrocatalysts templated by MOF for determination of levodopa

Journal

TALANTA
Volume 225, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2020.122042

Keywords

Single-atomic catalysts; Metal-organic frameworks; Electrochemical sensors; Drug monitoring; Levodopa

Funding

  1. National Natural Science Foundation of China [31730004]

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A new sensor based on a Co-single-atomic-site catalyst was developed for accurate determination of levodopa concentration in human fluids. The sensor exhibited superior electrochemical response, with a linear range of 0.1-200 μM and a limit of detection of 0.033 μM, making it a promising tool for clinical treatment of Parkinson's disease.
To overcome the problem of incorrect levodopa (LD) dosage in the treatment of Parkinson's disease, a new analytical tool is urgently needed for accurately determining the concentration of LD in human fluids. Herein, an effective and stable sensor based on a Co-single-atomic-site catalyst (Co-SASC)-modified glassy carbon electrode (Co-SASC/GCE) was developed for the determination of LD concentration. The physicochemical characterization of Co-SASC is systematically investigated. It has excellent thermal stability, graphitization degree, and a large specific surface area. Benefiting from its porous structure for kinetically fast catalysis and component advantages for fix a single cobalt atom to improve stability, Co-SASC/GCE exhibits a superior electrochemical response. Under optimal conditions (pH 2.0, coating amount is 10 mu g), an ideal linear relationship is achieved between the logarithm of the peak current of the sensor and the logarithm of LD concentration. The linear range is 0.1-200 mu M, and the limit of detection (LOD) is 0.033 mu M. After a simple pretreatment, LD in human serum is detected by Co-SASC/GCE with excellent stability and selectivity. As such, this work enlarges the existing electrochemical sensor toolbox by offering a reasonable design and synthesis protocol for advanced materials to accurately determine LD in human fluids for the clinical treatment of Parkinson's disease.

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