Hazards Monitoring Bionano Researh Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Korea.
Department of Nanobiotechnology, KRIBB School of Biotechnology, University of Science and Technology (UST), Daejeon 34113, Korea.
Sensors (Basel). 2018 Feb 15;18(2):598. doi: 10.3390/s18020598.
Aflatoxins (AFs) are highly toxic compounds that can cause both acute and chronic toxicity in humans. Aflatoxin B1 (AFB1) is considered the most toxic of AFs. Therefore, the rapid and on-site detection of AFB1 is critical for food safety management. Here, we report the on-site detection of AFB1 in grains by a portable surface plasmon resonance (SPR) sensor. For the detection of AFB1, the surface of an SPR Au chip was sequentially modified by cysteine-protein G, AFB1 antibody, and bovine serum albumin (BSA). Then, the sample solution and AFB1-BSA conjugate were flowed onto the Au chip in serial order. In the absence of AFB1, the SPR response greatly increased due to the binding of AFB1-BSA on the Au chip. In the presence of AFB1, the SPR response showed little change because the small AFB1 molecule binds on the Au chip instead of the large AFB1-BSA molecule. By using this portable SPR-based competitive immunoassay, the sensor showed low limits of detection (2.51 ppb) and quantification (16.32 ppb). Furthermore, we successfully detected AFB1 in rice, peanut, and almond samples, which suggests that the proposed sensing method can potentially be applied to the on-site monitoring of mycotoxins in food.
黄曲霉毒素(AFs)是毒性很高的化合物,可导致人类急性和慢性中毒。黄曲霉毒素 B1(AFB1)被认为是毒性最强的 AFs。因此,快速现场检测 AFB1 对食品安全管理至关重要。在这里,我们报告了一种便携式表面等离子体共振(SPR)传感器对谷物中 AFB1 的现场检测。为了检测 AFB1,SPR Au 芯片的表面依次用半胱氨酸蛋白 G、AFB1 抗体和牛血清白蛋白(BSA)修饰。然后,将样品溶液和 AFB1-BSA 缀合物依次流过 Au 芯片。在不存在 AFB1 的情况下,由于 Au 芯片上 AFB1-BSA 的结合,SPR 响应大大增加。在存在 AFB1 的情况下,SPR 响应几乎没有变化,因为小分子 AFB1 结合在 Au 芯片上而不是大分子 AFB1-BSA 分子上。通过使用这种基于便携式 SPR 的竞争性免疫测定法,传感器显示出较低的检测限(2.51 ppb)和定量限(16.32 ppb)。此外,我们成功地检测了大米、花生和杏仁样品中的 AFB1,这表明所提出的传感方法可能有潜力应用于食品中真菌毒素的现场监测。