化学
电化学
电化学气体传感器
卡那霉素
检出限
清脆的
组合化学
电极
杂交探针
纳米技术
DNA
抗生素
色谱法
生物化学
基因
材料科学
物理化学
作者
Xuemei Zhang,Li Zhu,Yang Li,Guoyu Liu,Shan Qiu,Xiaoli Xiong,Ke Huang,Ting Xiao,Liping Zhu
标识
DOI:10.1016/j.aca.2024.342562
摘要
A sensitive electrochemical platform was constructed with NH2–Cu-MOF as electrochemical probe to detect antibiotics using CRISPR/Cas12a system triggered by hybridization chain reaction (HCR). The sensing system consists of two HCR systems. HCR1 occurred on the electrode surface independent of the target, generating long dsDNA to connect signal probes and producing a strong electrochemical signal. HCR2 was triggered by target, and the resulting dsDNA products activated the CRISPR/Cas12a, thereby resulting in effective and rapid cleavage of the trigger of HCR1, hindering the occurrence of HCR1, and reducing the number of NH2–Cu-MOF on the electrode surface. Eventually, significant signal change depended on the target was obtained. On this basis and with the help of the programmability of DNA, kanamycin and ampicillin were sensitively detected with detection limits of 60 fM and 10 fM (S/N = 3), respectively. Furthermore, the sensing platform showed good detection performance in milk and livestock wastewater samples, demonstrating its great application prospects in the detection of antibiotics in food and environmental water samples.
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