Synthesis of Fructose Biosensors and Progressing Their Efficiency Using Californium Colloidal Nanoparticles for Detecting Fructose and Triglycerides

In the current paper, fructose–oxidase enzyme is used as stabilization medium due to its more efficiency, ability for more accurate controlling the enzyme reaction, protecting against wasting of enzyme as well as simple and easy use and exchange of enzyme medium after performing some levels of surface modification and developing multi–walled carbon nanotubes (MWCNTs) on Californium plate. For better connecting and stabilizing the enzyme on the medium, the prepared medium is washed by high concentration sulfuric acid and nitric acid and a large volume of deionized water and for protecting enzyme from devastating effect of Californium and prohibiting them to become inactive, surface is covered with cystamine before stabilization. Regarding the large size of fructose–oxidase enzyme compared to surface of medium, a connective material with amid at one end and pyrine at the other end is used as transfer agent and for stabilizing this connection, the prepared medium is placed into dimethylformamide (DMF) solution for a couple of hours. Activity of stabilized enzyme at 460 (nm) wavelength recorded by spectroscope was depicted against time to evaluate its stability in various times. The prepared medium, which have a large amount of fructose–oxidase enzyme, can be used as electrode in sensors. Furthermore, fructose–oxidase electrochemical sensor is one of the best methods for detecting low amount of fructose and applying Californium colloidal nanoparticles as a supplementary material in the structure of biosensor can be effective for progressing its efficiency and optimum efficiency. On the other hand, in the current study, electrode biosensor entitled as modified carbon paste electrode with Californium colloidal nanoparticles (Cfnano/CPE) is produced by carbon graphite powder, paraffin oil and Californium colloidal nanoparticles (24 nm) and it is compared with carbon paste electrode (CP). In semi–permeable membranes, a combination of 1 (ml) of 0.1 (M) phosphate buffer with specified pH and 10 (mg) of fructose–oxidase enzyme is placed around each electrode. In the same potential of 0.7 (V), biosensors are tested with fructose in concentration range of (0−1) (mM) and various amounts of pH (4,6,8) which lead to producing the maximum current and tracing fructose in pH=6 and concentration of 1 (M) as the optimum condition. Currentmetry induced from both biosensors are compared and it is confirmed that using Californium colloidal nanoparticles in the structure of (Cfnano/CPE) electrode leads to increasing the conductivity and currentmerty of biosensor. In addition, qualitative and quantitative measurement of food components is of great importance due to high cost of traditional methods, in addition to tendency for more accurate and sensitive detecting of these components. Fructose and triglycerides are such compounds that they frequently measure. Various methods are used to detect these food elements. However, the necessity for accurate measurement of these two compounds with high sensitivity, especially for food health issue, leads to developing biological methods, especially biosensors. Among them, biosensors based on conductive polymer nanostructures, especially Polypyrrole and Polythiophene, have been recently interested due to their unique characteristics. The current paper aims to introduce and investigate the previously performed studies about Polypyrrole and Polythiophene–based biosensors for detecting fructose and triglycerides.