ArticleFoods (Basel, Switzerland)2021
Development of Indirect Competitive ELISA and Visualized Multicolor ELISA Based on Gold Nanorods Growth for the Determination of Zearalenone.
Article in Foods (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Development of a Sensitive Enzyme Immunoassay Using Phage-Displayed Antigen-Binding Fragments for Zearalenone Detection in Cereal Samples.Foods (Basel, Switzerland) · 2025Article
- Ultrasensitive analyses of zearalenone in grain samples with a catalytic oxidation platform involving gold nanomaterials.Food chemistry: X · 2024Article
- Harnessing gold nanomaterials for advanced multicolor colorimetric biosensors in food hazards detection.Journal of food and drug analysis · 2024Review
- Nanomaterial-Based Optical Detection of Food Contaminants.Foods (Basel, Switzerland) · 2024Article
- Sensitive fluorescence ELISA for the detection of zearalenone based on self-assembly DNA nanocomposites and copper nanoclusters.Analytical and bioanalytical chemistry · 2024Article
- Article
- Preparation of Anti-Zearalenone IgY and Development of an Indirect Competitive ELISA Method for the Measurement of Zearalenone in Post-Fermented Tea.Foods (Basel, Switzerland) · 2023Article
- Antagonistic Activity of Oroxylin A againstToxins · 2023Article
- Review
- Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
In this study, a zearalenone (ZEN) hapten was designed and prepared against the mycotoxin ZEN, and the original coating ZEN-ovalbumin (ZEN-OVA) was prepared by conjugation with OVA. Based on the gold nanorods (AuNRs) of uniform size and stable properties synthesized by the seed-mediated method, the indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) and the AuNRs growth-based multicolor ELISA for detecting ZEN toxin were further established. Under the optimal experimental conditions, the coating amount of ZEN-OVA: 0.025 μg/well, antibody (Ab) dilution factor: 32,000 times, blocking solution: 0.5% skimmed milk powder, enzyme-labeled secondary Ab diluted 10,000 times, and a pH of the PBS buffer at 7.4, the sensitivity (
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