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用于多种霉菌毒素超灵敏化学发光免疫分析的成像传感器阵列与双信号放大策略相结合

Imaging sensor array coupled with dual-signal amplification strategy for ultrasensitive chemiluminescence immunoassay of multiple mycotoxins.

作者信息

Zong Chen, Jiang Fan, Wang Xiaoyu, Li Ping, Xu Linru, Yang Hua

机构信息

State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, PR China.

State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, PR China.

出版信息

Biosens Bioelectron. 2021 Apr 1;177:112998. doi: 10.1016/j.bios.2021.112998. Epub 2021 Jan 18.

Abstract

A novel chemiluminescence (CL) immunosensor array in combination with a dual-signal amplification strategy was developed for rapid and ultrasensitive detection of multiple mycotoxins in herbal medicine. The multi-component immunosensor array was constructed by immobilizing different bovine serum albumin combined mycotoxins on the corresponding sites of the aldehyde-modified glass slide. After competitive immunoreactions, CL triggered by signal tags captured on all the sensing sites can be collected by a charge-coupled device simultaneously for joint detection of several mycotoxins. By assembling a high ratio of horseradish peroxidase (HRP) and IgG on the surface of gold nanoparticles (AuNPs), a biofunctionalized complex named HRP@AuNP-IgG was prepared and served as the primary signal tag to amplify the CL signals. Then, by introducing tyramine signal amplification (TSA) technique, a new round of HRP could deposit around the HRP@AuNP-IgG, which brought the secondary CL amplification. As a proof of concept, the CL imaging sensor array was applied to the trace detection of citrinin, aflatoxin B and ochratoxins A in red yeast rice samples. Under optimal conditions, it exhibited wide linear ranges over 4 orders of magnitude and much lower limits of detection than previous works. Owing to the excellent sensitivity (50-57-fold signal amplification and detection limits down to sub-pM level), acceptable throughput (20 tests h), small amounts of reagents (3.5 μL for each test), simple sample pretreatment (no necessary of separation for 3 mycotoxins), high selectivity, acceptable stability and accuracy, the proposed sensing platform showed broad prospects in the joint monitoring of low-abundant mycotoxins and safety evaluation of herbal medicines.

摘要

开发了一种结合双信号放大策略的新型化学发光(CL)免疫传感器阵列,用于快速、超灵敏地检测草药中的多种霉菌毒素。通过将不同的牛血清白蛋白结合霉菌毒素固定在醛基修饰的载玻片相应位点上,构建了多组分免疫传感器阵列。竞争性免疫反应后,电荷耦合器件可同时收集所有传感位点上捕获的信号标签触发的CL,用于联合检测多种霉菌毒素。通过在金纳米颗粒(AuNPs)表面组装高比例的辣根过氧化物酶(HRP)和IgG,制备了一种名为HRP@AuNP-IgG的生物功能化复合物,作为初级信号标签来放大CL信号。然后,通过引入酪胺信号放大(TSA)技术,新一轮的HRP可沉积在HRP@AuNP-IgG周围,实现二次CL放大。作为概念验证,CL成像传感器阵列应用于红曲米样品中桔霉素、黄曲霉毒素B和赭曲霉毒素A的痕量检测。在最佳条件下,它显示出超过4个数量级的宽线性范围,检测限比以往工作低得多。由于具有出色的灵敏度(50-57倍信号放大,检测限低至亚皮摩尔水平)、可接受的通量(每小时20次测试)、少量试剂(每次测试3.5 μL)、简单的样品预处理(三种霉菌毒素无需分离)、高选择性、可接受的稳定性和准确性,所提出的传感平台在低丰度霉菌毒素的联合监测和草药安全性评价方面显示出广阔前景。

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