An immediate and antibody protected carboxyl quantum dot immunochromatographic analysis hierarchical signal amplification test strip based on biotin-streptavidin system for the detection of aflatoxin B1 in peanuts

Pub Date : 2023-10-10 DOI:10.1016/j.jfca.2023.105759
Bei Yuan , Qiang Liu , Qingqing Yang , Chengchen Pang , Haitao Xu , Xiaohui Du , Lin Wei , Kunying Nie , Yemin Guo , Xia Sun
{"title":"An immediate and antibody protected carboxyl quantum dot immunochromatographic analysis hierarchical signal amplification test strip based on biotin-streptavidin system for the detection of aflatoxin B1 in peanuts","authors":"Bei Yuan ,&nbsp;Qiang Liu ,&nbsp;Qingqing Yang ,&nbsp;Chengchen Pang ,&nbsp;Haitao Xu ,&nbsp;Xiaohui Du ,&nbsp;Lin Wei ,&nbsp;Kunying Nie ,&nbsp;Yemin Guo ,&nbsp;Xia Sun","doi":"10.1016/j.jfca.2023.105759","DOIUrl":null,"url":null,"abstract":"<div><p><span>As a relatively mature detection method, the test strip can quickly and sensitively detect the target. We designed an immunochromatographic strip based on biotin-streptavidin system to protect antibody (Ab) activity and achieve signal amplification. The coupling condition of biotin<span> (B) and antibody is relatively mild, which protects the activity of antibody. The high affinity between biotin and streptavidin (SA) and the one-to-many binding mode can connect multiple quantum dots (QDs) together to achieve a certain signal amplification effect. The coupling conditions of biotin and antibody (B-Ab), the working volume of QDs-SA and the volume of B-Ab were optimized. Under the optimal conditions, </span></span>aflatoxin B1 in peanut was detected. The detection range obtained by the experimental method was 1–10 μg/Kg, compared with the traditional quantum dot test strip method under the same conditions in this experiment, the amount of detection antibody is reduced and the detection range is increased. Compared with other immunochromatographic methods based on quantum dots to detect aflatoxin B1 (AFB1), the detection limit can reach the same order of magnitude, and the detection time is less.</p></div>","PeriodicalId":73752,"journal":{"name":"","volume":"125 ","pages":"Article 105759"},"PeriodicalIF":0.0,"publicationDate":"2023-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0889157523006336","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

As a relatively mature detection method, the test strip can quickly and sensitively detect the target. We designed an immunochromatographic strip based on biotin-streptavidin system to protect antibody (Ab) activity and achieve signal amplification. The coupling condition of biotin (B) and antibody is relatively mild, which protects the activity of antibody. The high affinity between biotin and streptavidin (SA) and the one-to-many binding mode can connect multiple quantum dots (QDs) together to achieve a certain signal amplification effect. The coupling conditions of biotin and antibody (B-Ab), the working volume of QDs-SA and the volume of B-Ab were optimized. Under the optimal conditions, aflatoxin B1 in peanut was detected. The detection range obtained by the experimental method was 1–10 μg/Kg, compared with the traditional quantum dot test strip method under the same conditions in this experiment, the amount of detection antibody is reduced and the detection range is increased. Compared with other immunochromatographic methods based on quantum dots to detect aflatoxin B1 (AFB1), the detection limit can reach the same order of magnitude, and the detection time is less.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
基于生物素-链霉亲和素系统的即时和抗体保护羧基量子点免疫色谱分析分级信号扩增试纸条检测花生中黄曲霉毒素B1
试纸条作为一种相对成熟的检测方法,能够快速灵敏地检测目标。我们设计了一种基于生物素-链霉亲和素系统的免疫层析条,以保护抗体(Ab)活性并实现信号放大。生物素(B)和抗体的偶联条件相对温和,保护了抗体的活性。生物素与链亲和素(SA)之间的高亲和力以及一对多结合模式可以将多个量子点连接在一起,从而达到一定的信号放大效果。优化了生物素与抗体(B-Ab)的偶联条件、量子点SA的工作体积和B-Ab的体积。在最佳条件下,对花生中的黄曲霉毒素B1进行了检测。该实验方法获得的检测范围为1–10μg/Kg,与本实验相同条件下的传统量子点试纸条法相比,检测抗体量减少,检测范围增加。与其他基于量子点的免疫层析方法检测黄曲霉毒素B1(AFB1)相比,检测极限可以达到相同数量级,检测时间更短。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1