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基于 FeMoO(OH) 的矿物水凝胶作为一种新型过氧化物酶纳米酶,通过比色传感器阵列用于灵敏和选择性检测芳香胺污染物。

FeMoO(OH)-based mineral hydrogels as a novel POD nanozyme for sensitive and selective detection of aromatic amines contaminants via a colorimetric sensor array.

机构信息

College of Materials Science and Engineering, Jilin Institute of Chemical Technology, Jilin 132022, China; College of Information Control Engineering, Jilin Institute of Chemical Technology, Jilin 132022, China.

College of Materials Science and Engineering, Jilin Institute of Chemical Technology, Jilin 132022, China.

出版信息

J Hazard Mater. 2024 May 5;469:133918. doi: 10.1016/j.jhazmat.2024.133918. Epub 2024 Feb 29.

Abstract

Developing convenient pathways to discriminate and identify multiple aromatic amines (AAs) remains fascinating and critical. Here, a novel three-channel colorimetric sensor array based on FeMoO(OH)-based mineral (FM) hydrogels is successfully constructed to monitor AAs in tap water. Benefiting from the substantial oxygen vacancies (V), FM nanozymes exhibit extraordinary peroxidase (POD)-like activities with K of 0.133 mM and V of 2.518 × 10 mM·s toward 3,3',5,5'-tetramethylbenzidine (TMB), which are much better than horseradish peroxidase and most of POD mimics. This reveals that doping Cu and Co into FM (FM-Cu and FM-Co) can change POD activity. Based on various POD activities, TMB and HO are used to generate fingerprint colorimetry signals from the colorimetry sensor array. The analytes can accurately discriminate through linear discriminant analysis, with a detection limit as low as 2.12 × 10-0.14 μM. The sensor array can effectively identify and discriminate AA contaminants and their mixtures and has performed well in real sample tests.

摘要

开发便捷的方法来区分和识别多种芳香胺(AAs)仍然是令人着迷和至关重要的。在这里,成功构建了一种基于基于 FeMoO(OH) 的矿物质 (FM) 水凝胶的新型三通道比色传感器阵列,以监测自来水中的 AAs。受益于大量的氧空位 (V),FM 纳米酶表现出非凡的过氧化物酶 (POD) 样活性,对 3,3',5,5'-四甲基联苯胺 (TMB) 的 K 为 0.133 mM,V 为 2.518×10 mM·s,优于辣根过氧化物酶和大多数 POD 模拟物。这表明掺杂 Cu 和 Co 到 FM 中(FM-Cu 和 FM-Co)可以改变 POD 活性。基于各种 POD 活性,TMB 和 HO 被用于从比色传感器阵列生成指纹比色信号。通过线性判别分析,可以准确区分分析物,检测限低至 2.12×10-0.14 μM。该传感器阵列可有效识别和区分 AA 污染物及其混合物,并在实际样品测试中表现良好。

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