The preparation and characterization of gold-coated magnetic particles are described for use as more efficient
solid-phase materials in immunoassay development. A
thin gold coating on commercial tosylated magnetic polystyrene particles (4.5 μm) is achieved via an electroless
plating method involving initial reaction of the particles
with Sn(II), followed by redox deposition of Ag0, that
serves as a catalytic site for the subsequent reduction of
Na3Au(SO3)2 in the presence of formaldehyde to yield the
adhered gold layer. Scanning electron microscopy, energy-dispersive X-ray analysis, and X-ray photoelectron spectroscopy indicate the presence of the desired Au0 outer
layer. To characterize the improved yield of antibody
binding sites on such gold-coated phases, the modified
particles are reacted with the free thiols of Fab‘ fragments
of an anti-alkaline phosphatase (ALP) antibody to orient
all the antigenic binding sites in a favorable direction.
After equilibration with ALP, the amount of ALP bound
to the surface of such particles is nearly 2.5-fold greater
than on non-gold-coated particles possessing the same
amount of immobilized anti-ALP Fab‘, but oriented randomly on the surface. The new gold-coated magnetic
particles are further used as a solid phase for developing
a sandwich-type enzyme immunoassay to detect C-reactive
protein (CRP) using horseradish peroxidase as the enzyme label. The gold-coated magnetic particles with anti-CRP monoclonal Fab‘ reagents provide assays with enhanced assay slope (1.8-fold), lower nonspecific adsorption, and a detection limit improvement of nearly 10-fold
(0.14 vs 1.9 ng/mL) compared to the same Fab‘ anti-CRP
immobilized on the initial tosylated polystyrene magnetic
particles. The improved assay performance is attributed
to the more favorable binding orientation of the self-assembled monolayer of Fab‘ fragments on the gold-coated particles compared to the random orientation on
the non-gold-coated surfaces