Gold nanoparticles (AuNPs) are the
most commonly used signal materials
in lateral flow immunoassay (LFIA). However, the assay sensitivity
of traditional AuNP-based LFIA is usually limited by the incomplete
competition between free target analytes and immobilized antigens
for the binding of AuNP-labeled antibodies. To unfreeze this limitation,
here, asymmetric Au–SiO2 Janus NPs (about 66 nm)
were designed and synthesized. Au–SiO2 Janus NPs
can assemble into snowman-like anisotropic structures and combine
two different physicochemical properties at their opposite sides,
where the AuNP side mainly possesses the antibody conjugating and
signal providing functions and the SiO2 side primarily
offers the stable function. In virtue of the unique asymmetric nanostructure,
only the AuNP side can interact with target analytes by specific antigen–antibody
interactions, which could significantly improve the efficiency of
competition. Selecting furazolidone as a model analyte, the immunoassay
biosensor showed a limit of detection as low as 0.08 ng/mL, 10-fold
decreased than that of the AuNPs-LFIA. Moreover, the Au–SiO2 Janus NP lateral flow immunoassay was well applied in chicken,
pork, honey, and beef food samples with visual detection limits of
0.8 ng/g, 0.16 ng/g, 0.4 ng/mL, and 0.16 ng/g, respectively. The Au–SiO2 Janus NPs possess the advantages of both materials, which
will broaden their applications as a potential alternative in the
rapid and sensitive detection of antibiotic residues.