Abstract
This paper reports the determination of aflatoxin B1 (AFB1), one of the most carcinogenic substances known. A multi-commuted flow injection–solid phase spectroscopy (FI–SPS) system combined with photochemically induced fluorescence (PIF) was developed, for the first time, for its quantitative determination. A strongly fluorescent degradation product was obtained on-line by irradiation with ultraviolet light. The determination was carried out by measuring the fluorescence intensity of the photo-product at 353/424 (λ ex/λ em), once retained on C18 silica-gel filling the flow-cell. A linear dynamic range of 0.09–12 µg l−1, detection limit as sensitive as 29 ng l−1 and a relative standard deviation (RSD) of 1.4% were obtained. The method proposed was satisfactorily applied to the determination of AFB1 in different types of beer (normal and non-alcoholic). Hydrophobic compounds were eliminated from beer samples and AFB1 was extracted with acetonitrile by solid-phase extraction on C18 sorbent. Recoveries of the target compound from spiked beers were between 94 and 106%. The results obtained in the analysis of real samples are in good agreement with those provided by a reference chromatographic method.
Acknowledgements
The authors acknowledge the financial support from “Consejería de Innovación, Ciencia y Empresa” (Junta de Andalucía), Project P07-FQM-02673. LMG also acknowledges a research fellowship from the Spanish MEC.