4.7 Article

Innovative electrochemical platform for the simultaneous determination of l-DOPA and l-tyrosine using layer-by-layer assembled L-proline-linked nanodiamonds on printed graphene

Journal

MICROCHIMICA ACTA
Volume 190, Issue 10, Pages -

Publisher

SPRINGER WIEN
DOI: 10.1007/s00604-023-05970-1

Keywords

L-DOPA; L-Tyrosine; Nanodiamond; Poly(L-proline); Electrochemical sensor; Differential pulse voltammetry

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This study aimed to develop an innovative and simple electrochemical sensor for melanoma and related disorders using the simultaneous determination of l-DOPA and l-Tyr. The sensor was fabricated by layer-by-layer electrodeposition of nanodiamond and poly L-proline onto a graphene electrode. The modified electrodes showed improved sensitivity and the ability to exclude interfering substances. The sensor demonstrated good performance in the detection of l-DOPA and l-Tyr in human urine and blood serum samples.
Discovering alternative analytical techniques is crucial for practical applications; thus, this work aims to develop an innovative and simple electrochemical sensor for melanoma and the clinical diagnosis of related disorders by the simultaneous deter-mination of 3,4-dihydroxy-l-phenylalanine (l-DOPA) and l-tyrosine (l-Tyr). The fabrication is based on the layer-by-layer electrodeposition of poly l-proline (poly(L-pro)) and nanodiamond (ND) onto a screen-printed graphene electrode (SPGE). The poly(l-pro)/ND/SPGEs were morphologically characterized by scanning electron microscopy, energy-dispersive X-ray spectrometry, and Raman spectroscopy followed by electrochemical investigation using cyclic voltammetry, differential pulse voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. These modifier-based electrodes pave a feasible way to unlock the coexisting interfering substances from screen-printing ink composition and improve the sensitivity. Additionally, computational chemistry calculations were performed to fully comprehend the sensing behavior on both target analytes. Under optimal conditions, the developed sensor provided linear concentration ranges of 0.075-50 p.M, with a detection limit of 0.021 p.M for l-DOPA, and 2.5-120 p.M with a detection limit of 0.74 p.M for l-Tyr. To demon-strate the reliability of the poly(l-pro)/ND/SPGE in practical application, it was successfully applied to the determination of these analytes in human urine and blood serum samples, with satisfactory recovery ranges (81.73-110.62% for l-DOPA and 82.17-110.01% for l-Tyr) and relative standard deviations (0.69-9.90% for l-DOPA and 0.40-9.55% for l-Tyr). Due to its simplicity, long-term stability (> 87.8% of their initial currents after 35 days), and portability, the developed sensor is a promising alternative analytical method for on-site clinical monitoring.

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