4.6 Article

A ratiometric electrochemical biosensor via alkaline phosphatase mediated dissolution of nano-MnO2 and Ru(III) redox recycling for the determination of dimethoate

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ELSEVIER
DOI: 10.1016/j.jpba.2021.114400

关键词

Alkaline phosphatase; Nano-MnO2; Ratiometric electrochemical biosensor; Redox recycling; Dimethoate

资金

  1. National Natural Science Foundations of China [21964004, 22164005]
  2. Natural Science Foundation of Guangxi [2018GXNSFBA050053, 2018GXNSFBA281053, AD19110004]
  3. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources [CMEMR2019-A05]
  4. BAGUI Scholar Program

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A sensitive and ratiometric electrochemical biosensor was developed for the determination of dimethoate via alkaline phosphatase (ALP) mediated dissolution of nano-MnO2 and [Ru(NH3)(6)](3+)(Ru(III)) redox recycling. The biosensor showed good performance in detecting dimethoate with high sensitivity and a detection limit of 6.3 pg mL(-1).
A sensitive and ratiometric electrochemical biosensor was developed for the determination of dimethoate via alkaline phosphatase (ALP) mediated dissolution of nano-MnO2 and [Ru(NH3)(6)](3+)(Ru(III)) redox recycling. The electroactive probe Ru(III) was adsorbed on the nano-MnO2 with the high specific surface area through electrostatic interaction to form the MnO2-Ru(III) nanocomposite, which was then fixed on the surface of the glassy carbon electrode. When the dimethoate inhibited the catalytic activity of ALP in a homogeneous system, the hydrolysate L-ascorbic acid (AA) produced by ALP hydrolysis of L-ascorbic acid-trisodium 2-phosphate (AAP) decreased. The solution was then incubated with a glassy carbon electrode modified by MnO2-Ru(III). At this time, only a small amount of MnO2-Ru(III) was decomposed and Ru(III) was rapidly electroreduced to Ru(II) on the surface of the electrode. The in-situ produced Ru(II) was chemically oxidized back to Ru(III) by Fe(III). The redox recycling of Ru(III) was completed and the Ru(III) reduction current signal was amplified. The process consumed part of Fe(III) to reduce the reduction current signal of Fe(III), and the ratio of the two reduction currents (I-Ru(III)/I-Fe((III))) increased significantly. The (I-Ru(III)/I(Fe)((III) )value increased with the increase of dimethoate concentration in the linear range of 0.01-300 ng mL(-1), and the detection limit was 6.3 pg mL(-1). It has been successfully applied to the determination of dimethoate in oilseed rape and lettuce with a satisfactory result. (C) 2021 Elsevier B.V. All rights reserved.

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