Fe3O4 @polydopamine-based microchannel resistance immunosensor for detecting deoxynivalenol in wheat samples

文献类型: 外文期刊

第一作者: Peng, Xuewen

作者: Peng, Xuewen;Dong, Yongzhen;Feng, Niu;Wei, Qiaoling;Lu, Peng;Chen, Yiping;Dong, Yongzhen;Chen, Yiping;Peng, Xuewen;Dong, Yongzhen;Feng, Niu;Wei, Qiaoling;Lu, Peng;Chen, Yiping;Chen, Yiping

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关键词: Blocking effect; Deoxynivalenol; Magnetic separation carrier; Microchannel resistance immunosensor

期刊名称:SENSORS AND ACTUATORS B-CHEMICAL ( 影响因子:8.4; 五年影响因子:7.2 )

ISSN:

年卷期: 2023 年 378 卷

页码:

收录情况: SCI

摘要: Food security problems caused by deoxynivalenol in grains have aroused widespread concern. Rapid analysis of deoxynivalenol still suffers from complex operation, low sensitivity, and insufficient accuracy. Herein, the Fe3O4 @polydopamine (PDA) nanoparticle with a core-shell structure was synthesized, which could conveniently conjugate the antibody of deoxynivalenol, thus forming a novel immunomagnetic separation carrier Fe3O4 @PDA-antibody for the specific enrichment of the target. Furthermore, the Fe3O4 @PDA-antibody nano-recognizer could act as the elicitor to activate the aggregation of complete antigen (BSA-deoxynivalenol) func-tionalized polystyrene (PS) beads through the antigen-antibody reaction. The aggregated Fe3O4 @PDA-antibody-antigen-PS immunocomplex was driven into the microchannel by the electroosmotic flow, inducing a remarkable change in current due to the blocking effect, which was related to the amount of deoxynivalenol. In this approach, Fe3O4 @PDA-antibody nanoparticles integrated extraction, immuno-reaction, and detection effec-tively, and the microchannel resistance sensor (MCRS) could immediately monitor the change in the current. The whole process could be completed within 1 h, which improved the efficiency and decreased the interference. This Fe3O4 @PDA-antibody-mediated MCRS was developed for the ultrasensitive detection of deoxynivalenol with a linear range of 0.05 -1000 ng/mL, and the limit of detection (LOD) was 20.7 pg/mL, which was a 21-fold enhancement compared with the enzyme-linked immunosorbent assay, providing a tool for hazardous target analysis.

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