Affinity capture of aflatoxin B-1 and B-2 by aptamer-functionalized magnetic agarose microspheres prior to their determination by HPLC

A novel adsorbent is described for magnetic solid-phase extraction (MSPE) of the aflatoxins AFB(1) and AFB(2) (AFBs). Magnetic agarose microspheres (MAMs) were functionalized with an aptamer to bind the AFBs which then were quantified by HPLC and on-line post-column photochemical derivatization with fluorescence detection. Streptavidin-conjugated MAMs were synthesized first by a highly reproducible strategy. They possess strong magnetism and high surface area. The MAMs were characterized by transmission electron microscopy, scanning electron microscopy, optical microscopy, laser diffraction particle size analyzer, Fourier transform infrared spectrometry, vibrating sample magnetometry and laser scanning confocal microscopy. Then, the AFB-aptamers were immobilized on MAMs through biotin-streptavidin interaction. Finally, the MSPE is performed by suspending the aptamer-modified MAMs in the sample. They are then collected by an external magnetic field and the AFBs are eluted with methanol/buffer (20:80). Several parameters affecting the coupling, capturing and eluting efficiency were optimized. Under the optimized conditions, the method is fast, has good linearity, high selectivity, and sensitivity. The LODs are 25 pg.mL(-1) for AFB(1) and 10 pg.mL(-1) for AFB(2). The binding capacity is 350 +/- 8 ng.g(-1) for AFB(1) and 384 +/- 8 ng.g(-1) for AFB(2), and the precision of the assay is < 8%. The method was successfully applied to the analysis of AFBs in spiked maize samples.