A colorimetric immunoassay based on glucose oxidase-induced AuNP aggregation for the detection of fumonisin B1

化学 检出限 伏马菌素B1 肉眼 色谱法 葡萄糖氧化酶 胶体金 过氧化氢 辣根过氧化物酶 免疫分析 分析物 纳米颗粒 生物传感器 生物化学 真菌毒素 纳米技术 材料科学 免疫学 抗体 生物 食品科学
作者
Xirui Chen,Yi Liang,Wenjing Zhang,Yuankui Leng,Yonghua Xiong
出处
期刊:Talanta [Elsevier]
卷期号:186: 29-35 被引量:52
标识
DOI:10.1016/j.talanta.2018.04.018
摘要

Naked-eye readout colorimetric signal-based assays are promising for high-throughput screening detection and point-of-care diagnostics in resource-constrained regions. Here, a novel direct competitive plasmonic enzyme-linked immunosorbent assay (dc-pELISA) based on gold nanoparticle (AuNP) aggregation with highly sensitive and robust naked-eye readout signal was developed and used to detect fumonisin B1 (FB1). AuNP aggregation was induced by a horseradish peroxidase (HRP)/hydrogen peroxide (H2O2)/tyramine (TYR) system, resulting in a dramatic color change from red to blue. In this system, H2O2 was produced via GOx-mediated glucose oxidation reaction, and FB1-GOx was used as a competitive antigen. The proposed pELISA demonstrated good linear detection of FB1 from 3.125 ng mL-1 to 25 ng mL-1 with a vivid color change from deep blue to red and a cutoff limit of 12.5 ng mL-1 observed by the naked eye. The average recoveries for FB1-spiked corn samples ranged from 76.5% to 96.8% with a relative standard derivation of 4.88~ 16.4%. Meanwhile, the proposed method exhibited excellent agreement (R2 = 0.927) with the conventional ELISA method in blindly detecting FB1 spiked corn samples. Additionally, the results of the proposed method for FB1 positive corn samples also showed a high consistency with those of the ultra performance liquid chromatography method. These results indicated acceptable accuracy and precision of the proposed colorimetric ELISA for quantitative detection of FB1 in actual corn samples.
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