Plasmonic ELISA based on enzyme-assisted etching of Au nanorods for the highly sensitive detection of aflatoxin B1 in corn samples

• Published in: Sensors and actuators. B, Chemical Vol. 267; pp. 320 - 327
• Main Authors: Xiong, Ying, Pei, Ke, Wu, Yunqing, Duan, Hong, Lai, Weihua, Xiong, Yonghua
• Format: Journal Article
• Language: English
• Published: Lausanne Elsevier B.V 15.08.2018; Elsevier Science Ltd
• Subjects: Aflatoxin B1; Aspect ratio; Coefficient of variation; Colorimetric detection; Corn; Etching; Glucose; Glucose oxidase; Gold; Gold nanorod; Hydrogen peroxide; Immunoassay; Liquid chromatography; Mass spectrometry; Morphology; Mycotoxins; Nanomaterials; Nanorods; Optical density; Organic chemistry; Peroxidase; Plasmonic ELISA; Pollutants; Pollution monitoring; Product safety; Qualitative analysis; Sensitivity; Toxins; Aflatoxin B1; Glucose oxidase; Gold nanorod; Plasmonic ELISA; Colorimetric detection
• ISSN: 0925-4005; 1873-3077
• DOI: 10.1016/j.snb.2018.04.027

[Display omitted] •The HRP-assisted etching method using AuNRs as signal output of pELISA for AFB1 quantitative or qualitative detection.•The proposed pELISA exhibited a high sensitivity for AFB1 visual detection with a cut-off limit of 12.5 pg/mL.•The proposed method shows great potential for trace amounts of AFB1 detection by the naked eye in resource-constrained regions. In this work, we reported an advanced enzyme-assisted etching method using gold nanorods (AuNRs) as signal output of plasmonic enzyme-linked immunosorbent assay (pELISA) for the quantitative or qualitative detection of aflatoxin B1 (AFB1) in real corn samples. AFB1-labeled glucose oxidase was adopted as the competing antigen to catalyze glucose into H2O2. Meanwhile, horseradish peroxidase was employed to catalyze H2O2 and hence generate .OH. The AuNRs with the aspect ratio of 2:1 were chemically etched by OH to a rod-like morphology. This occurrence reduced the optical density at 650 nm and resulted in a vivid color response from bluish-green to red easily detectable by a microplate reader for quantitative AFB1 analysis or by the naked eye for qualitative AFB1 detection. Various parameters that may influence the detection performance of pELISA were investigated. The proposed method showed an extremely high sensitivity for qualitative AFB1 detection, with a visible cut-off value of 12.5 pg/mL. The technique also achieved a good linear range of 3.1–150 pg/mL for quantitative AFB1 analysis, with a half-maximal inhibitory concentration of 22.3 pg/mL, which was approximately 32 folds lower than those of conventional ELISA (707 pg/mL). The average recoveries for corn samples spiked with different concentrations of AFB1 ranged from 82% to 115%, with a coefficient of variation that ranged from 2% to 13%. These values corresponded to an acceptable accuracy and precision for the proposed method. In addition, the reliability of the proposed method was further confirmed by the liquid chromatography–tandem mass spectrometry (LC–MS/MS) method. In brief, this work offers an improved screening strategy with high sensitivity and robustness for the qualitative or quantitative detection of mycotoxins or other pollutants in food safety monitoring.