Development of soft chemical processes for the synthesis of interfacial architectures with well-defined structural nano-motifs organized over large areas in two dimensions is an important branch of nanotechnology. The present study deals with the fabrication of gold nanostructures using size-selective chemical etching of continuous gold films on glass support with titanium and chromium adhesive layers. In this process, which is called self-passivated surface etching, a gold film is etched in the presence of citric acid, resulting in gold nanostructures adhering to the metal support. The size-controlled chemical dissolution of gold is driven by a competing reaction between self-organized passivation of surface nano-motifs by citric acid shells and soft etching by a nonoxidative composition containing hydrochloric acid and hydrogen peroxide in water. According to these results, the presence of a chemically stable adhesive layer (titanium), citric acid in solution, and agitation are critical factors to be considered. However, the nature of the adhesive layer is the most influential factor. The following technique presents a simple method for the rapid fabrication of a nanostructured gold substrate that has the ability to support both propagating and localized surface plasmon resonances simultaneously.
Plasmonics 2010, 5, (4), 395-403.

The use of instrumental systems based on the surface plasmon resonance (SPR) for rapid diagnosis of intact plant viruses (in particular, tobacco mosaic virus (TMV)) is considered. A new approach using detection of viral antigen and antibody (IgG) complexes formed during the preincubation step (instead of their consecutive application in classical approach) is discussed. A comparison between signal level registered from the mixture of virus and specific serum and that from the sample without virus (samples deposited onto the sensor surface treated with thiocyanate and protein A Staphylococcus aureus) allows unambiguous detection of viral particles in the material studied. The performance capabilities of the method are discussed and illustrated by quantitative detection of virus in the actual samples (cells homogenate) at high concentration.
Journal of virological methods, 2004. – V121. – P.101-106.