A planar array immunosensor, equipped with a charge-coupled device (CC
D) as a detector, was used to simultaneously detect 3 toxic analytes.
Wells approximately 2 mm in diameter were formed on glass slides using
a photoactivated optical adhesive. Antibodies against staphylococcal
enterotoxin B (SEB), ricin, and Yersinia pestis were covalently attach
ed to the bottoms of the circular wells to form the sensing surface. R
ectangular wells containing chicken immunoglobulin were used as alignm
ent markers and to generate control signals. After removing the optica
l adhesive, the slides were mounted over a scientific grade CCD operat
ing at ambient temperature in inverted (multipin phasing) mode. A two-
dimensional graded index of refraction lens at-ray was used to focus t
he sensing surface onto the CCD. Solutions of toxins were then placed
on the slide. After rinsing, Cy5-labeled antibodies were introduced. T
he identity and amount of toxin bound at each location on the slide we
re determined by quantitative image analysis. Concentrations as low as
25 ng/mL of ricin, 15 ng/mL of pestis F1 antigen, and 5 ng/mL of SEB
could be routinely measured. (C) 1998 Elsevier Science S.A. All rights
reserved.