基于链霉亲和素诱导金纳米颗粒聚集的黄曲霉毒素B1比色/荧光双模免疫测定方法的建立

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Yaqian Cheng, Chenxi Wang, Xueyu Chang, Xuexia Jia, Zesheng Liu, Baolin Liu, Zhixian Gao, Huanying Zhou
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引用次数: 0

摘要

基于链霉亲和素诱导的金纳米颗粒聚集,建立了黄曲霉毒素B1 (AFB1)比色和荧光检测的双模式免疫分析方法(AuNP@SA)。合成了aunp修饰的链亲和素-生物素标记AFB1完全抗原聚集体(AuNP@SA@Bio-BSA-AFB1)作为竞争结合双模探针。AuNP@SA@Bio-BSA-AFB1聚集物具有高比色和荧光猝灭强度。采用AFB1抗体修饰的免疫磁微球作为捕获探针。AFB1与AuNP@SA@Bio-BSA-AFB1之间的竞争性结合导致颜色和荧光强度的变化。比色法的检出限为6.95 ng·mL−1,荧光法的检出限为0.07 ng·mL−1。通过测定花生样品中的AFB1,证明了所提出策略的实用性。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a colorimetric/fluorescence dual-mode immunoassay for aflatoxin B1 based on streptavidin-induced gold nanoparticle aggregation

A dual-mode immunoassay method was developed for colorimetric and fluorescence detection of aflatoxin B1 (AFB1) based on streptavidin-induced gold nanoparticle aggregation (AuNP@SA). AuNP-modified streptavidin–biotin labeling AFB1 complete antigen aggregations (AuNP@SA@Bio-BSA-AFB1) were synthesized as the competitive binding and dual-mode probe. AuNP@SA@Bio-BSA-AFB1 aggregations possessed high colorimetric and fluorescence quenching intensities. AFB1 antibodies modified immunomagnetic microspheres were used as the capture probe. The competitive binding between AFB1 and AuNP@SA@Bio-BSA-AFB1 leads to changes in color and fluorescence intensity. The detection limit of the colorimetric method is 6.95 ng·mL−1, while that of the fluorescence method is 0.07 ng·mL−1. The practicality of the proposed strategy was demonstrated by determining AFB1 in spiked peanut samples.

Graphical Abstract

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来源期刊
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
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