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)
生物传感器
杀虫剂
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 B. 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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