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Updated: Jan 18, 2026

ELIME Enzyme Linked Immuno Magnetic Electrochemical Method for Mycotoxin Detection
Published on: October 23, 2009
Electron transfer-driven bismuth-gold nanozyme-enhanced aptamer-based lateral flow assay for simultaneous detection
Yu Li1, Yiyao Wu1, Zhouping Wang2
1State Key Laboratory of Food Science and Resources, Jiangnan University, Wuxi, 214122, China; Key Laboratory of Screening, Prevention, and Control of Food Safety Risks, State, Administration for Market Regulation, Wuxi, Jiangsu, 214122, China; School of Food Science and Technology, Jiangnan University, Wuxi, 214122, China.
Background:
The co-contamination of aflatoxin M1 (AFM1) and ochratoxin A (OTA) poses an increased risk to human health due to their synergistic toxic effects, necessitating the development of sensitive and multiplex mycotoxins analytical methods.
Results:
An aptamer-based multiplex lateral flow assay (Apt-MLFA) was developed employing bimetallic bismuth-gold nanoparticles (BiAuNPs) to facilitate the simultaneous detection of AFM1 and OTA. The BiAuNPs were synthesized through in-situ deposition, demonstrating exceptional peroxidase-mimicking activity and storage stability. Specifically, the Bi of valence-rich and Au of high electron transfer efficiency endowed BiAuNPs with high peroxidase-mimicking activity, which oxidized 3,3',5,5'-tetramethylbenzidine through electron transfer. These nanoparticles were further functionalized with AFM1-and OTA-specific aptamers, which served as molecular recognition and signal amplification probes. Complementary DNAs were immobilized as dual test lines to enable a competitive detection system. By combining nanozyme-based signal amplification with smartphone-based analytical device, the assay demonstrated detection limits of detection of 0.11 ng/mL for AFM1 and 0.15 ng/mL for OTA, along with a linear detection range of 0.5-500 ng/mL. Also, this Apt-MLFA was successfully applied to real samples with satisfactory recoveries.
Significance:
This strategy effectively integrates bimetallic nanoparticle signal amplification, aptamer-specific recognition, and spatially separated dual test lines, thereby providing a robust platform for on-site multiplex screening of mycotoxins in food samples.
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