Summary An enzyme‐linked immunosorbent assay (ELISA) using a monoclonal antibody was established to detect aflatoxin B 1 (AFB 1 ) in tea. The antibody was prepared from a hybridoma derived by fusing Sp2/0‐Ag14 myeloma cells and immunised spleen B cells. The effects from pH , ionic strength, and organic solvents on immunoassay were optimised and the 50% inhibition (IC 50 ) value was 0.057 ± 0.007 ng mL −1 . Spiked black and green tea samples at 10, 20 and 50 ng g −1 levels of AFB 1 were detected with this proposed ELISA. The recoveries for black tea samples ranged from 68.5% to 117.7% and 73.5 to 114.3% for green tea samples. This immunoassay showed no cross‐reactions with other mycotoxin family but good recognition with related aflatoxins. These results indicate that the ELISA assay could be used as a screening method for aflatoxin detection in tea samples.
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Zhang et al. (2013) studied this question.
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