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双金属纳米酶-酶混合材料介导的用于食品中黄曲霉毒素 B 检测的高灵敏和自动免疫测定法。

Bimetallic nanozyme-bioenzyme hybrid material-mediated ultrasensitive and automatic immunoassay for the detection of aflatoxin B in food.

机构信息

College of Engineering, Huazhong Agricultural University, Wuhan, 430070, PR China.

College of Food Science and Technology, Huazhong Agricultural University, Wuhan, 430070, PR China.

出版信息

Biosens Bioelectron. 2024 Mar 15;248:115992. doi: 10.1016/j.bios.2023.115992. Epub 2024 Jan 3.

Abstract

Aflatoxin B (AFB) is one of the most prevalent and dangerous biotoxin in crops and feedstuff, which poses a great threat to human health and also cause significant financial losses. Therefore, there is an urgent need to develop an effective method for AFB detection. In this work, we developed an automatic reaction equipment and nanozyme-enhanced immunosorbent assay (Auto-NEISA) for sensitive and accurate detection of AFB by combining the highly effective signal probes with a self-designed automated immunoreactive equipment. Wherein, polystyrene (PS) nanoparticles were used as signal carriers for loading a massive in situ-synthesized platinum and palladium bimetallic nanozyme, which could enrich horseradish peroxidase-labeled goat anti-mouse antibody (HRP-Ab) on the nanozyme surface to form a bimetallic nanozyme-bioenzyme hybrid material for multiple signal amplification. The entire reaction could be automatically completed by the self-developed immunoreactive equipment. The Auto-NEISA method realized the sensitive detection of AFB with a wide linear detection range of 10-10 pg/mL, at a low limit of detection (LOD) of 5.52 pg/mL. The LOD was 65-fold lower than that of the enzyme-linked immunosorbent assay (ELISA). Additionally, Auto-NEISA was successfully applied to detect AFB in real food samples, demonstrating that it has considerable potential for detecting food contaminants with high accuracy and efficiency.

摘要

黄曲霉毒素 B(AFB)是农作物和饲料中最普遍和最危险的生物毒素之一,对人类健康构成了极大威胁,同时也造成了巨大的经济损失。因此,迫切需要开发一种有效的 AFB 检测方法。在这项工作中,我们开发了一种自动反应设备和纳米酶增强免疫吸附测定(Auto-NEISA),通过结合高效信号探针和自主设计的自动化免疫反应设备,实现了对 AFB 的灵敏和准确检测。其中,聚苯乙烯(PS)纳米粒子被用作信号载体,用于负载大量原位合成的铂和钯双金属纳米酶,可将辣根过氧化物酶标记的山羊抗鼠抗体(HRP-Ab)富集到纳米酶表面,形成双金属纳米酶-酶的杂交材料,实现多重信号放大。整个反应可以通过自主开发的免疫反应设备自动完成。Auto-NEISA 方法实现了对 AFB 的灵敏检测,线性检测范围为 10-10 pg/mL,检测限(LOD)低至 5.52 pg/mL。LOD 比酶联免疫吸附测定(ELISA)低 65 倍。此外,Auto-NEISA 成功应用于检测实际食品样品中的 AFB,表明它具有高准确度和高效率检测食品污染物的巨大潜力。

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