A surface plasmon resonance (SPR) immunosensor is developed to determine concentrations of the mycotoxin, fumonisin B1 (FB1), in spiked samples. Polyclonal antibodies produced against FB1 are adsorbed onto a thin gold film substrate, which is coupled to a glass prism in the Kretschmann configuration. The output beam of a planar light-emitting diode is focused through the prism to excite SPR at the surface of the gold film. When a sample containing FB1 is added to a cell on the outside of the gold film, the angular profile of reflected light intensity shifts. This changes the resonance angle and the reflected beam intensity at a selected angle, both of which are proportional to the FB1 concentration. After optimization of the antibody overlayer, a detection limit of 50 ng/mL is obtained for the direct assay with an analysis time under 10 min. Multiple sample additions and large-volume sample circulation can be used with the high-affinity antibodies to achieve lower detection limits.

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Persistent URL dx.doi.org/10.1006/abio.1998.2616
Journal Analytical Biochemistry
Mullett, W. (Wayne), Lai, E. P, & Yeung, J.M. (Jupiter M.). (1998). Immunoassay of fumonisins by a surface plasmon resonance biosensor. Analytical Biochemistry, 258(2), 161–167. doi:10.1006/abio.1998.2616