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基于金纳米棒生长的间接竞争ELISA和可视化多色ELISA用于玉米赤霉烯酮测定的方法开发

Development of Indirect Competitive ELISA and Visualized Multicolor ELISA Based on Gold Nanorods Growth for the Determination of Zearalenone.

作者信息

Ma Tianyu, Liu Kaixin, Yang Xiao, Yang Jingying, Pan Mingfei, Wang Shuo

机构信息

State Key Laboratory of Food Nutrition and Safety, Tianjin University of Science & Technology, Tianjin 300457, China.

Key Laboratory of Food Nutrition and Safety, Ministry of Education of China, Tianjin University of Science and Technology, Tianjin 300457, China.

出版信息

Foods. 2021 Nov 2;10(11):2654. doi: 10.3390/foods10112654.

Abstract

In this study, a zearalenone (ZEN) hapten was designed and prepared against the mycotoxin ZEN, and the original coating ZEN-ovalbumin (ZEN-OVA) was prepared by conjugation with OVA. Based on the gold nanorods (AuNRs) of uniform size and stable properties synthesized by the seed-mediated method, the indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) and the AuNRs growth-based multicolor ELISA for detecting ZEN toxin were further established. Under the optimal experimental conditions, the coating amount of ZEN-OVA: 0.025 μg/well, antibody (Ab) dilution factor: 32,000 times, blocking solution: 0.5% skimmed milk powder, enzyme-labeled secondary Ab diluted 10,000 times, and a pH of the PBS buffer at 7.4, the sensitivity () of the established ic-ELISA for ZEN detection reached 0.85 ± 0.04 μg/L, and the limit of detection () reached 0.22 ± 0.08 μg/L. In the multicolor ELISA based on the growth of AuNRs, as the content of ZEN increased, the mixed solution exhibited a significant color change from brownish red to colorless. ZEN concentration as low as 0.1 μg/L can be detected by the naked eye (brown red to dark gray). This study provided an effective analysis strategy for the rapid screening and accurate monitoring of the ZEN contaminant in foods.

摘要

在本研究中,设计并制备了一种针对玉米赤霉烯酮(ZEN)霉菌毒素的半抗原,并通过与卵清蛋白(OVA)偶联制备了原始包被物ZEN-卵清蛋白(ZEN-OVA)。基于种子介导法合成的尺寸均匀且性质稳定的金纳米棒(AuNRs),进一步建立了用于检测ZEN毒素的间接竞争酶联免疫吸附测定(ic-ELISA)和基于AuNRs生长的多色ELISA。在最佳实验条件下,即ZEN-OVA包被量为0.025μg/孔、抗体(Ab)稀释倍数为32000倍、封闭液为0.5%脱脂奶粉、酶标二抗稀释10000倍且PBS缓冲液pH为7.4时,所建立的用于检测ZEN的ic-ELISA的灵敏度()达到0.85±0.04μg/L,检测限()达到0.22±0.08μg/L。在基于AuNRs生长的多色ELISA中,随着ZEN含量的增加,混合溶液呈现出从棕红色到无色的显著颜色变化。肉眼可检测到低至0.1μg/L的ZEN浓度(从棕红色变为深灰色)。本研究为食品中ZEN污染物的快速筛查和准确监测提供了一种有效的分析策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e6/8619891/dfd50658b73b/foods-10-02654-sch001.jpg

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