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基于 FeO@Cu 纳米酶过氧化物酶样活性的特异性抑制作用对草甘膦的机制研究及比色-化学发光双模式检测。

Mechanistic investigation and dual-mode colorimetric-chemiluminescent detection of glyphosate based on the specific inhibition of FeO@Cu nanozyme peroxidase-like activity.

机构信息

School of Food and Bioengineering, Xihua University, Chengdu 610039, China; Food Microbiology Key Laboratory of Sichuan Province, China.

School of Food and Bioengineering, Xihua University, Chengdu 610039, China.

出版信息

Food Chem. 2024 Jun 15;443:138501. doi: 10.1016/j.foodchem.2024.138501. Epub 2024 Jan 18.

Abstract

In this study, a dual-mode colorimetric/CL nanosensor was developed for glyphosate detection based on the specific inhibition of FeO@Cu peroxidase-like activity. Synthesized FeO@Cu exhibited high levels of peroxidase-like activity that triggered the oxidation of luminol/3,3',5,5'-tetramethyl benzidine dihydrochloride (TMB) to excited-state 3-aminophthalic acid/blue oxTMB, thereby delivering a CL signal/visible colorimetric signal, however, the presence of glyphosate inhibited this activity, resulting in a decrease in signal strength. In-depth investigation revealed that this inhibitory mechanism occurs via two pathways: one in which glyphosate chelates with Fe(III)/Cu(II) and occupy the catalytical active sites of FeO@Cu, thereby decreasing the generation of OH, and another in which glyphosate competes with TMB to consume generated OH, thus reducing the oxidation of TMB. This mechanism formed the basis of our novel dual-mode colorimetric/CL glyphosate nanosensor, which achieved limits of detection (LODs) of 0.086 µg/mL and 0.019 µg/mL in tests, thus demonstrating its significant potential for on-site glyphosate monitoring.

摘要

在这项研究中,开发了一种基于 FeO@Cu 过氧化物酶样活性的特异性抑制的双模式比色/CL 纳米传感器用于草甘膦检测。合成的 FeO@Cu 表现出高水平的过氧化物酶样活性,触发了发光氨/3,3',5,5'-四甲基联苯胺二盐酸盐(TMB)的氧化,生成激发态 3-氨基邻苯二甲酸/蓝色 oxTMB,从而提供 CL 信号/可见比色信号,然而,草甘膦的存在抑制了这种活性,导致信号强度降低。深入研究表明,这种抑制机制通过两种途径发生:一种途径是草甘膦与 Fe(III)/Cu(II)螯合并占据 FeO@Cu 的催化活性位点,从而减少 OH 的生成,另一种途径是草甘膦与 TMB竞争消耗生成的 OH,从而减少 TMB 的氧化。这种机制构成了我们新型双模式比色/CL 草甘膦纳米传感器的基础,在测试中实现了 0.086µg/mL 和 0.019µg/mL 的检测限(LOD),因此证明了其在现场草甘膦监测方面的巨大潜力。

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