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Fumonisin B1 (FB1) is a toxin produced by the metabolism of Fusarium oxysporum, which can cause serious effects on the nervous, respiratory, digestive, and reproductive systems of humans or animals; it is known as one of the highly toxic epidemic contaminants. Herein, we report the visual inspection of FB1 using bipolar electrodes (BPEs) with an array-based electrochemiluminescence (ECL) platform. The sensor consists of a PDMS cover and a glass substrate containing an array of 10 ITO electrodes. A specific sensing interface was constructed on the cathode of the BPE, which could modulate the ECL reactions that occurred at the anode of BPEs. To amplify the ECL signal, methylene blue (MB)-encapsulated Zr-MOFs (MB@Zr-MOFs) were synthesized and immobilized on the cathode of the BPE, which could amplify the ECL signal at the anode. By coupling the cyclic amplification effect of the DNA walker and nicking endonuclease (Nb.BbvCI), the biosensor can realize the visual measurement of FB1 in the range of 5 × 10−5~0.5 ng/mL. In addition, the developed biosensor was used to monitor the concentration of FB1 in maize and peanut samples. The recoveries were in the range of 99.2%~110.6%, which demonstrated the good accuracy of the designed BPE-ECL biosensor for FB1 assay in food samples. [ABSTRACT FROM AUTHOR]

Rapid and efficient detection of mycotoxins is of great significance in the field of food safety. In this review, several traditional and commercial detection methods are introduced, such as high-performance liquid chromatography (HPLC), liquid chromatography/mass spectrometry (LC/MS), enzyme-linked immunosorbent assay (ELISA), test strips, etc. Electrochemiluminescence (ECL) biosensors have the advantages of high sensitivity and specificity. The use of ECL biosensors for mycotoxins detection has attracted great attention. According to the recognition mechanisms, ECL biosensors are mainly divided into antibody-based, aptamer-based, and molecular imprinting techniques. In this review, we focus on the recent effects towards the designation of diverse ECL biosensors in mycotoxins assay, mainly including their amplification strategies and working mechanism. [ABSTRACT FROM AUTHOR]