Testing Technology Company of Changsha Research Institute of Mining and Metallurgy Co., Ltd., Changsha 410012, China.
Laboratory of Micro & Nano Biosensing Technology in Food Safety, Hunan Provincial Key Laboratory of Food Science and Biotechnology, College of Food Science and Technology, Hunan Agricultural University, Changsha 410128, China.
Anal Methods. 2024 May 16;16(19):3088-3098. doi: 10.1039/d3ay02330c.
Herein, a novel fluorescent/colorimetric/photothermal biosensor is proposed for aflatoxin B1 (AFB1) detection in food based on Prussian blue nanoparticles (PBNPs) (∼50 nm), gold nanoclusters (AuNCs), and an aptamer (Apt) within three hours. Briefly, a multifunctional compound, namely PBNPs-PEI@AuNCs, was synthesized from PBNPs as the loading carrier, polyethyleneimine (PEI) as the cross-linking agent, and AuNCs directly combined on the surface of PBNPs. The AFB1 Apt was then modified on the PBNPs-PEI@AuNCs to form a PBNPs-PEI@AuNCs-Apt probe, whereby when AFB1 is present, AFB1 is specifically captured by the probe. Meanwhile, the MNPs@antibody was also introduced to capture AFB1, thereby forming a "sandwich" structure compound. After magnetic separation, high temperature was applied to this "sandwich" structure compound to induce the denaturation of the Apt. Then the fluorescent/colorimetric/photothermal signals were collected from the PBNPs-PEI@AuNCs@Apt to give information on its related condition. The detection limits of the biosensor were 0.64 × 10, 0.96 × 10, and 0.55 × 10 g mL for the three signals, which were outputted independently and could be verified with each other to ensure the accuracy of the results. Moreover, the colorimetric and photothermal strategies with this probe do not require large-scale instruments, providing a promising choice for achieving the rapid field detection of AFB1.
本文提出了一种基于普鲁士蓝纳米粒子(PBNPs)(∼50nm)、金纳米簇(AuNCs)和适体(Apt)的新型荧光/比色/光热生物传感器,用于在三小时内检测食品中的黄曲霉毒素 B1(AFB1)。简而言之,从 PBNPs 作为负载载体、聚乙烯亚胺(PEI)作为交联剂和直接结合在 PBNPs 表面的 AuNCs 合成了一种多功能化合物,即 PBNPs-PEI@AuNCs。然后将 AFB1 Apt 修饰在 PBNPs-PEI@AuNCs 上,形成 PBNPs-PEI@AuNCs-Apt 探针,当存在 AFB1 时,探针特异性捕获 AFB1。同时,还引入了 MNPs@抗体来捕获 AFB1,从而形成“三明治”结构化合物。在磁分离后,将高温施加于该“三明治”结构化合物,以诱导 Apt 的变性。然后从 PBNPs-PEI@AuNCs@Apt 收集荧光/比色/光热信号,以提供其相关条件的信息。该生物传感器的检测限分别为 0.64×10、0.96×10 和 0.55×10 g/mL,三种信号独立输出,并可相互验证,以确保结果的准确性。此外,该探针的比色和光热策略不需要大型仪器,为实现 AFB1 的快速现场检测提供了有前途的选择。