Brucellosis is an infectious disease that spreads easily between animals and even human beings. There is a critical fact that once a flock of livestocks is infected by Brucella, the prevalent brucellosis would cause over half of the infected pregnant ones to abort. 1 A sensitive and simple detection of Brucella antibody is essential in clinic and veterinary diagnosis. Some traditional diagnostic procedures, such as bacterioscopy (BS), agglutination test (AT), complement fixation test (CFT), precipitation reaction test (PRT), SPA-co-agglutination test (SCAT), enzyme-linked immunosorbent assay (ELISA), radio immunoassay (RIA) and indirect fluorescent antibody (IFAT) test, have been employed in clinical analysis. 2 However, some of these approaches are rather time-consuming or requiring highly qualified personnel; others depend on sophisticated instrumentation. Moreover, most of these procedures are only adapted for the qualitative or semiquantitative detection for Brucella assays. To obtain satisfactory results, most of the diagnostic procedures have to be coupled with another independent test; otherwise, a part of the infected samples may escape the screening test. Developing new, simple and more sensitive quantitative diagnosis methods has attracted the considerable interest.Electrochemical immunosensors are robust tools of immunoanalytical means that have been the subject of continued research and development in recent years. These methods generally involve the production or use of an electrochemical active substance for signal generation.Immunoenzymatic sensors involving the enzyme label and the specificity of an antigen-antibody binding have an effect of chemical amplification and relatively high selectivity. The advantages of electrochemical immunosensors include speed, accuracy, selectivity and sensitivity. paraffin, 6 nafion, 7 chitosan, 8 were used as a matrix material to prepare immunosensors. They are mostly organic polymers, which tend to swell when dipped into a solvent, leading to a shift of the response signal. The activity of biomolecules in these materials used for immobilization decreases appreciably and the immobilized biomolecules do not retain their activity over a long time period. Recently, in the so-called sol-gel process, some biomaterials were trapped into a silicate glass matrix under mild conditions. [10][11][12] Biomolecules show considerable retention of their activity in such immobilization matrices. The other outstanding feature of such a process is that small substrate molecules can diffuse into the pores of the polymeric silica matrix and reach the site of the bioreagent. The Sol-Gel process for biomolecules immobilization seems to be very promising, especially due to the mild conditions that are used for the immobilization process as well as the simplicity of the procedure involved.
13In addition, the immobilization material can be optimized so that transparent monoliths, thin films or fine particles, are formed depending on the ultimate application of the preparation. 14-17 Brau...