4.7 Article

Direct competitive ELISA enhanced by dynamic light scattering for the ultrasensitive detection of aflatoxin B1 in corn samples

期刊

FOOD CHEMISTRY
卷 342, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2020.128327

关键词

Dynamic light scattering; Enzyme-linked immunosorbent assay; Glucose oxidase; Ultrasensitive detection; Aflatoxin B-1

资金

  1. National Key Research and Development Program of China [2018YFC1602203, 2018YFC1602202]
  2. National Natural Science Foundation of China [31760485]
  3. Opening Fund of Jiangsu Key Laboratory for Food Quality and Safety-State Key Laboratory Cultivation Base, Ministry of Science and Technology [028074911709]

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The study introduced a novel DLS-dcELISA technology for detecting AFB(1) in corn, which exhibited ultrahigh sensitivity and excellent selectivity. By amplifying the AuNP scattering signals, the technique can significantly improve the accuracy and practicality of detection. The developed method has the potential to replace traditional approaches and enhance competitive detection of mycotoxins.
Compared with absorbance, scattering-based dynamic light scattering (DLS) signal has higher sensitivity because its light-scattering intensity is very sensitive to changes in size, thereby enhancing the sensitivity. Herein, we first developed a DLS-enhanced direct competitive enzyme-linked immunosorbent assay (DLS-dcELISA) for ultra sensitive detection of aflatoxin B-1 (AFB(1)) in corn. By using hydroxyl radical-induced gold nanoparticle (AuNP) aggregation to amplify AuNP scattering signals, the developed DLS-dcELISA exhibited ultrahigh sensitivity for AFB(1). The detection limit was 0.12 pg mL(-1), which was 153and 385-fold lower than those obtained using plasmonic and colorimetric dcELISA. In addition, the DLS-dcELISA exhibited excellent selectivity, high accuracy, and strong practicality. Overall, this work presented a simple and universal strategy for improving the sensitivity of traditional ELISA platform only by using the sensitive DLS signals. This technique can replace absorbancebased plasmonic or colored signals as immunoassay signal output for enhanced competitive detection of mycotoxins.

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