4.7 Article

Selective inhibition toward the enzyme-like activity of 3D porous cerium-doped graphene oxide nanoribbons for highly sensitive and enzyme-free colorimetric detection of pesticides

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SENSORS AND ACTUATORS B-CHEMICAL
卷 378, 期 -, 页码 -

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2022.133130

关键词

Carbon-based nanocomposite; Nanozyme; Diafenthiuron; Carbaryl; Dual enzyme-like activities

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A 3D porous cerium-doped graphene oxide nanoribbons with dual enzyme-like activities were prepared and used for the selective colorimetric detection of diafenthiuron and carbaryl. The detection method achieved a linear range of 10-1500 ng/mL for diafenthiuron and 2-800 ng/mL for carbaryl, with detection limits of 0.57 and 0.23 ng/mL, respectively. This work provides a new approach for developing highly sensitive and selective pesticide detection based on the direct inhibition of nanozyme activity through non-metal-sulfur bonding.
The development of the detection method based on directly inhibiting nanozyme activity holds great promise for on-site monitoring pesticide contamination of foods, while rarely investigated. In this work, a 3D porous cerium -doped graphene oxide nanoribbons (Ce-GONRs) with dual enzyme-like activities (peroxidase and oxidase) were prepared, which could synergistically catalyze the oxidation of TMB. Diafenthiuron and carbaryl were found to selectively inhibit the dual enzyme-like activities of Ce-GONRs, ascribing to 7C-7C stacking and hydrogen bond between pesticides with nanozymes. Based on this mechanism, the enzyme-free colorimetric detection for dia-fenthiuron and carbaryl were developed. The linear range of diafenthiuron and carbaryl were 10-1500 ng/mL and 2-800 ng/mL, and the detection limits (LOD) of these were 0.57 and 0.23 ng/mL, respectively. The method was successfully applied to detect diafenthiuron and carbaryl in apple and lake water samples. In addition, this work opened up a new way for developing highly sensitive and selective pesticide detection based on the direct inhibition of nanozyme activity through non-metal-sulfur bonding.

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