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通过靶标诱导生成多价DNA纳米线检测黄曲霉毒素B1的灵敏比色测定法加速了催化发夹组装反应。

Sensitive colorimetric assay for the detection of aflatoxin B1 via target-induced generation of multivalent DNA nanowires accelerates the catalytic hairpin assembly reaction.

作者信息

Zhang Shihong, Sun Yingying, Liu Xingyu, Chen Cong, Ma Yuhan, Yu Dian, Liu Wenjie, Yu Jianna, Jing Guoxing, Liu Wen, Li Wenshan

机构信息

College of Chemical Engineering, Xiangtan University, Xiangtan, 411105, China.

College of Chemical Engineering, Xiangtan University, Xiangtan, 411105, China.

出版信息

Anal Chim Acta. 2025 Nov 1;1373:344490. doi: 10.1016/j.aca.2025.344490. Epub 2025 Jul 29.

Abstract

BACKGROUND

Aflatoxin B1 (AFB1) is a highly carcinogenic mycotoxin frequently found in contaminated food products, posing a significant threat to public health and food safety. Therefore, the development of rapid, sensitive, and reliable detection methods for AFB1 is critical for early warning and prevention. However, traditional detection techniques often require expensive equipment, skilled personnel, and complex procedures, limiting their suitability for on-site applications. This study introduces a novel colorimetric assay based on DNA nanotechnology to enhance sensitivity, reduce cost, and simplify the detection process for broader applicability.

RESULTS

The colorimetric assay for AFB1 detection that utilizes a target-induced generation of multivalent DNA nanowires, which in turn accelerate a catalytic hairpin assembly (CHA) reaction. Upon binding to AFB1, the DNA nanowires are formed and act as multivalent scaffolds that significantly enhance the speed of the CHA process. Compared to the use of free T strand and monovalent DNA nanowires, the multivalent design increased the initial reaction rate by 7.6-fold and 32.3-fold, respectively. This enhanced reaction kinetics, driven by the multivalent effect, led to improved signal amplification in the target-induced cascade reaction. The assay demonstrated a strong linear correlation between absorbance and the logarithm of AFB1 concentration over a dynamic range of 10 pM to 1 nM. Furthermore, the method achieved a low detection limit of 4.26 pM. Recovery rates in spiked peanut samples ranged from 95.96 % to 107.75 %, confirming its reliability in complex food matrices.

SIGNIFICANCE

This assay provides a highly sensitive method for detecting AFB1 without the need for sophisticated instruments or specialized training. Its simple visual readout and portability make it particularly advantageous for on-site testing. By leveraging multivalent DNA nanowires and CHA amplification, this assay holds great promise not only for AFB1 detection but also for broader applications in food safety monitoring and mycotoxin control.

摘要

背景

黄曲霉毒素B1(AFB1)是一种高致癌性霉菌毒素,经常在受污染的食品中发现,对公众健康和食品安全构成重大威胁。因此,开发快速、灵敏且可靠的AFB1检测方法对于早期预警和预防至关重要。然而,传统检测技术通常需要昂贵的设备、技术熟练的人员和复杂的程序,限制了它们在现场应用中的适用性。本研究引入了一种基于DNA纳米技术的新型比色测定法,以提高灵敏度、降低成本并简化检测过程,从而实现更广泛的应用。

结果

用于检测AFB1的比色测定法利用目标诱导生成多价DNA纳米线,进而加速催化发夹组装(CHA)反应。与AFB1结合后,形成DNA纳米线并作为多价支架,显著提高CHA过程的速度。与使用游离T链和单价DNA纳米线相比,多价设计分别将初始反应速率提高了7.6倍和32.3倍。这种由多价效应驱动的增强反应动力学,导致目标诱导级联反应中的信号放大得到改善。该测定法在10 pM至1 nM的动态范围内,吸光度与AFB1浓度的对数之间呈现出很强的线性相关性。此外,该方法实现了4.26 pM的低检测限。加标花生样品中的回收率在95.96%至107.75%之间,证实了其在复杂食品基质中的可靠性。

意义

该测定法提供了一种无需复杂仪器或专业培训即可检测AFB1的高灵敏方法。其简单的视觉读数和便携性使其在现场检测中特别具有优势。通过利用多价DNA纳米线和CHA扩增,该测定法不仅在AFB1检测方面具有巨大潜力,而且在食品安全监测和霉菌毒素控制的更广泛应用中也具有广阔前景。

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