4.7 Article

In Situ Synthesis of a Bismuth Vanadate/Molybdenum Disulfide Composite: An Electrochemical Tool for 3-Nitro-L-Tyrosine Analysis

Journal

INORGANIC CHEMISTRY
Volume 61, Issue 35, Pages 14046-14057

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c02037

Keywords

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Funding

  1. Ministry of Science and Technology [MOST-108-2221-E-027-063]
  2. National Taipei University of Technology (NTUT)

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This study develops a highly sensitive electrode material for the detection of NO2-Tyr by integrating the unique features of BiVO4 and MoS2. The MoS2@BiVO4 heterojunction exhibits excellent electrochemical behavior, allowing for the measurement of NO2-Tyr in biological media without time-consuming pretreatments. The synergistic interactions between BiVO4 and MoS2 contribute to low resistance charge transfer, a good response range, and a lower limit of detection for NO2-Tyr.
The quantification of 3-nitro-L-tyrosine (NO2-Tyr), an in vivo biomarker of nitrosative stress, is indispensable for the clinical intervention of various inflammatory disorders caused by nitrosative stress. By integrating the unique features of BiVO4 and MoS2 with matching bandgap energies, electrode materials with amplified response signals can be developed. In this regard, we introduce a hydrothermally synthesized bismuth vanadate sheathed molybdenum disulfide (MoS2@ BiVO4) heterojunction as a highly sensitive electrode material for the determination of NO2-Tyr. Excellent electrochemical behavior perceived for the MoS2@BiVO4 augments the performance of the sensor and allows the measurement of NO2-Tyr in biological media without any time-consuming pretreatments. The synergistic inter-actions between BiVO4 and MoS2 heterojunctions contribute to low resistance charge transfer (Rct = 159.13 omega.cm2), a reduction potential Epc = -0.58 V (vs Ag/AgCl), and a good response range (0.001-526.3 mu M) with a lower limit of detection (0.94 nM) toward the detection of NO2-Tyr. An improved active surface area, reduced charge recombination, and high analyte adsorption contribute to the high loading of the biomarker for improved selectivity (in the presence of 10 interfering compounds), operational stability (1000 s), and reproducibility (six various modified electrodes). The proposed sensor was successfully utilized for the real-time determination of NO2-Tyr in water, urine, and saliva samples with good recovery values (+/- 98.94-99.98%), ascertaining the reliability of the method. It is noteworthy that the electrochemical activity remains unaffected by other redox interferons, thus leading to targeted sensing applications.

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