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基于纳米颗粒的竞争磁性免疫检测法用于灵敏的黄曲霉毒素 B1 检测。

Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection.

机构信息

Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074 Aachen, Germany.

Institute of Biological Information Processing, Bioelectronics IBI-3, Forschungszentrum Jülich, 52428 Jülich, Germany.

出版信息

Toxins (Basel). 2020 May 20;12(5):337. doi: 10.3390/toxins12050337.


DOI:10.3390/toxins12050337
PMID:32443933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7290995/
Abstract

Food and crop contaminations with mycotoxins are a severe health risk for consumers and cause high economic losses worldwide. Currently, different chromatographic- and immuno-based methods are used to detect mycotoxins within different sample matrices. There is a need for novel, highly sensitive detection technologies that avoid time-consuming procedures and expensive laboratory equipment but still provide sufficient sensitivity to achieve the mandated detection limit for mycotoxin content. Here we describe a novel, highly sensitive, and portable aflatoxin B1 detection approach using competitive magnetic immunodetection (cMID). As a reference method, a competitive ELISA optimized by checkerboard titration was established. For the novel cMID procedure, immunofiltration columns, coated with aflatoxin B1-BSA conjugate were used for competitive enrichment of biotinylated aflatoxin B1-specific antibodies. Subsequently, magnetic particles functionalized with streptavidin can be applied to magnetically label retained antibodies. By means of frequency mixing technology, particles were detected and quantified corresponding to the aflatoxin content in the sample. After the optimization of assay conditions, we successfully demonstrated the new competitive magnetic detection approach with a comparable detection limit of 1.1 ng aflatoxin B1 per ml sample to the cELISA reference method. Our results indicate that the cMID is a promising method reducing the risks of processing contaminated commodities.

摘要

食物和农作物受到真菌毒素污染会对消费者的健康造成严重威胁,并在全球范围内造成巨大的经济损失。目前,不同的色谱和免疫方法被用于检测不同样品基质中的真菌毒素。需要新型的、高灵敏度的检测技术,这些技术避免了耗时的程序和昂贵的实验室设备,但仍具有足够的灵敏度,以达到真菌毒素含量的法定检测限。在这里,我们描述了一种使用竞争性磁性免疫检测(cMID)的新型、高灵敏度和便携式黄曲霉毒素 B1 检测方法。作为参考方法,通过棋盘滴定法优化了竞争性 ELISA。对于新型的 cMID 程序,使用包被了黄曲霉毒素 B1-BSA 结合物的免疫过滤柱进行生物素化黄曲霉毒素 B1 特异性抗体的竞争性富集。随后,可以应用带有链霉亲和素的磁性颗粒来对保留的抗体进行磁性标记。通过频率混合技术,可以根据样品中的黄曲霉毒素含量检测和定量颗粒。在优化了测定条件后,我们成功地用与 cELISA 参考方法相当的检测限(1.1 ng 黄曲霉毒素 B1/ml 样品)证明了新的竞争性磁性检测方法的可行性。我们的结果表明,cMID 是一种很有前途的方法,可以降低处理受污染商品的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d2a59076caa0/toxins-12-00337-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/79ffca0cf6f2/toxins-12-00337-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d758a8ed4646/toxins-12-00337-g0A2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d5251f320e3d/toxins-12-00337-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/bb5df8df2d57/toxins-12-00337-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/76b67ae17d2f/toxins-12-00337-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/27975044a9c8/toxins-12-00337-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d819831f1461/toxins-12-00337-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d2a59076caa0/toxins-12-00337-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/79ffca0cf6f2/toxins-12-00337-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d758a8ed4646/toxins-12-00337-g0A2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d5251f320e3d/toxins-12-00337-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/bb5df8df2d57/toxins-12-00337-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/76b67ae17d2f/toxins-12-00337-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/27975044a9c8/toxins-12-00337-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d819831f1461/toxins-12-00337-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2629/7290995/d2a59076caa0/toxins-12-00337-g006.jpg

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Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection.

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[7]
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[8]
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[9]
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本文引用的文献

[1]
Validation of an LC-MS/MS-based dilute-and-shoot approach for the quantification of > 500 mycotoxins and other secondary metabolites in food crops: challenges and solutions.

Anal Bioanal Chem. 2020-2-20

[2]
An Automated and High-Throughput Immunoaffinity Magnetic Bead-Based Sample Clean-Up Platform for the Determination of Aflatoxins in Grains and Oils Using UPLC-FLD.

Toxins (Basel). 2019-10-10

[3]
Novel analytical methods to study the fate of mycotoxins during thermal food processing.

Anal Bioanal Chem. 2019-10-21

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Worldwide contamination of food-crops with mycotoxins: Validity of the widely cited 'FAO estimate' of 25.

Crit Rev Food Sci Nutr. 2019-9-3

[5]
Sensitive and rapid detection of cholera toxin subunit B using magnetic frequency mixing detection.

PLoS One. 2019-7-5

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Mycotoxin Testing Paradigm: Challenges and Opportunities for the Future.

J AOAC Int. 2019-11-1

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3D Printed Modular Immunofiltration Columns for Frequency Mixing-Based Multiplex Magnetic Immunodetection.

Sensors (Basel). 2019-1-3

[8]
DNA damage checkpoint response to aflatoxin B1.

Environ Toxicol Pharmacol. 2018-12-7

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Aflatoxin B1: A review on metabolism, toxicity, occurrence in food, occupational exposure, and detoxification methods.

Food Chem Toxicol. 2018-11-20

[10]
Development of Methods for Determination of Aflatoxins.

Crit Rev Food Sci Nutr. 2016-12-9

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