Rapid and selective detection of AFB1 by direct mass spectrometry using immunoaffinity paper substrate

An antibody-modified Teslin paper was prepared in combination with direct mass spectrometry for the rapid and sensitive analysis of trace aflatoxin B1 (AFB1) in grain and its related products. Antibodies were covalently immobilized to Teslin surface by glutaraldehyde method, and an immunoaffinity paper substrate (IAP) was obtained. IAP can not only be used as a carrier for enrichment of analytes, but also coupled with the MS inlet for desorption/ionization detection. Compared to antibody-free Teslin, IAP could have excellent selectivity for the enrichment of AFB1. It took less than 1 min for detection. Among the matrices (wheat flour, peanut oil and corn), the proposed method showed satisfactory selectivity and linearity. The LOD and LOQ were 0.40-0.80 mu g kg(-1) and 1.20 mu g kg(-1), respectively. In conclusion, the IAP can provide a new powerful tool for rapid and sensitive analysis of mycotoxins.

Automated summary

An antibody-modified Teslin paper was used in combination with direct mass spectrometry for rapid and sensitive analysis of trace aflatoxin B1. The developed immunoaffinity paper showed excellent selectivity for enrichment and efficient detection of the target analyte.