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Rolling circle amplified DNAzyme followed with covalent organic frameworks: Cascade signal amplification of electrochemical ELISA for alfatoxin M1 sensing

机译:滚动圆升级DNAzyme随后是共价有机框架:用于阿法罗蛋白M1感测的电化学ELISA的级联信号放大

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摘要

A sensitive, selective and high-throughput electrochemical enzyme-linked immunosorbent assay (EC-ELISA) platform was constructed for determination of alfatoxin M1 (AFM1). Rolling circle amplified (RCA) DNAzyme coupled with covalent organic frameworks (COFs) modified electrode was used as signal amplification strategies. The immunoreaction was performed on a microplate via specific recognition of AFM1 by primer-AuNPs-aptamer and anti-AFM1 antibody. The primer triggered RCA reaction produced a long single-stranded DNA, which can fold into a peroxidase-mimicking DNAzyme with the presence of hemin and K+. In the presence of H2O2, DNAzyme catalyzed the oxidation of 2-aminophenol and the oxidation product 3-aminophenylhydrazine was enriched as a signal molecule on the TpBD modified electrode with a significant current response. Under optimized conditions, the sensor exhibited high selectivity and sensitivity towards AFM1 with a detection limit of 0.15 ng/mL. In addition, the AFM1 can also be quantified by the naked eye. This EC-ELISA platform was successfully applied for the determination of AFM1 in milk samples with recoveries from 93.37% to 104.01%. (C) 2020 Elsevier Ltd. All rights reserved.
机译:构建了一种敏感,选择性和高通量的电化学酶联免疫吸附测定(EC-ELISA)平台用于测定阿法罗蛋白M1(AFM1)。滚动圆扩增(RCA)与共价有机骨架(COF)改性电极偶联的滚动圈(RCA)DNAzyme用作信号放大策略。通过引物-AUnps-Aptamer和抗AFM1抗体对微孔板进行免疫层对微孔板进行。引物触发的RCA反应产生了长的单链DNA,其可以在血红素和K +存在下折叠成过氧化物酶 - 模拟DNAzyme。在H 2 O 2的存在下,DNazyme催化了2-氨基苯酚的氧化,氧化产物3-氨基苯基肼在TPBD改性电极上富集为信号分子,具有显着的电流反应。在优化的条件下,传感器对AFM1的选择性和灵敏度表现出高,检测限为0.15ng / ml。此外,AFM1也可以通过肉眼量化。此EC ELISA平台成功地应用于牛奶样品中的AFM1,回收率为93.37%至104.01%。 (c)2020 elestvier有限公司保留所有权利。

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