鉴定(生物学)
生物系统
生化工程
材料科学
计算机科学
新烟碱
人工智能
机器学习
农药残留
纳米技术
信号(编程语言)
杀虫剂
生物传感器
铅(地质)
环境化学
催化作用
信号处理
双酚A
人工酶
组合化学
漆酶
工作(物理)
作者
Qingluan Li,Zhizhong Sun,Min Chen,Lijuan Xie,Yibin Ying
标识
DOI:10.1021/acsami.6c00511
摘要
Residues of neonicotinoid insecticides (NEOs) pose serious threats to ecological systems and human health. Conventional nanozyme sensors often suffer from limited catalytic diversity and concentration-dependent response mechanisms, which lead to signal homogenization and cross-concentration misclassification. To address these limitations, we developed a Fe-Cu dual-atom nanozyme (FeCu DAzyme) exhibiting triple-enzyme activities: oxidase (OXD), peroxidase (POD), and laccase (LAC). The synergistic effects between Fe-Cu dual-atom sites significantly enhanced catalytic efficiency, while their specific coordination with NEO functional groups enabled distinct inhibition responses across different concentration levels. Leveraging this property, we constructed a FeCu DAzyme-based colorimetric sensor array that captures real-time inhibition kinetics of OXD/POD/LAC activities, generating unique multidimensional response patterns. Through integration with a machine learning classifier, these patterns enabled accurate pesticide identification independent of absolute concentration values. The sensor array achieved 92.50% accuracy in discriminating five NEO structural analogs across a concentration range of 0.1-50 μg/mL, demonstrating excellent concentration-independent identification capability. Notably, the practical utility of this platform was successfully validated through the high-accuracy identification of NEOs in spiked real-world samples, including lake water and agricultural products. This work established a promising paradigm for rapid NEO identification, which is critical for ensuring agricultural product safety.
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