Chen Ziyue, Bai Lei, Xie Xinhua, Zhang Xinhao, Wen Shuaiqi, Qin Jieqiong, Zhang Shichang, Zhang Bobo, Zhu Hongshuai
Henan Agricultural University, Zhengzhou, 450002, China.
Key Laboratory for Staple Grain Processing, Ministry of Agriculture and Rural Affairs, Zhengzhou, 450002, China.
Mikrochim Acta. 2025 Sep 5;192(10):635. doi: 10.1007/s00604-025-07509-y.
A dual-mode aptasensor was engineered for aflatoxin B (AFB) detection by functional integration of peroxidase-mimetic Au@CeO core-shell nanostructures with emissive carbon dots (CDs). The Au@CeO nanocomposite, synthesized via spontaneous redox reaction, exhibited enhanced peroxidase-like activity due to abundant Ce/oxygen vacancies facilitating hydroxyl radical generation. The aptasensor utilizes a competitive binding mechanism, where AFB competed with immobilized Au@CeO-CDs-Apt1 probes for binding sites, resulting in inversely proportional colorimetric and fluorescent signals. Under optimized conditions, the biosensor achieved a broad linear detection range (0.001-50 ng/mL) with an ultralow limit of detection (LOD) of 0.0005 ng/mL. The sensor demonstrated excellent selectivity, stability, and reproducibility, and was successfully applied to detect AFB in spiked peanut samples, with recoveries ranging from 98.7 to 116.7%. This work not only advances the design of nanozyme-based biosensors but also provides a rapid, accurate, and field-deployable strategy for monitoring mycotoxins in complex food matrices.
通过将过氧化物酶模拟物Au@CeO核壳纳米结构与发光碳点(CDs)功能整合,构建了一种用于黄曲霉毒素B(AFB)检测的双模式适体传感器。通过自发氧化还原反应合成的Au@CeO纳米复合材料,由于丰富的Ce/氧空位促进了羟基自由基的产生,表现出增强的过氧化物酶样活性。该适体传感器利用竞争结合机制,其中AFB与固定化的Au@CeO-CDs-Apt1探针竞争结合位点,导致比色和荧光信号成反比。在优化条件下,该生物传感器实现了宽线性检测范围(0.001-50 ng/mL),超低检测限(LOD)为0.0005 ng/mL。该传感器表现出优异的选择性、稳定性和重现性,并成功应用于加标花生样品中AFB的检测,回收率在98.7%至116.7%之间。这项工作不仅推动了基于纳米酶的生物传感器设计,还为监测复杂食品基质中的霉菌毒素提供了一种快速、准确且可现场部署的策略。