Abstract
In this work, a magneto-biosensor based on iron (II, III) oxide (magnetite, Fe3O4) nanoparticles for the detection of uric acid is developed and demonstrated. These Fe3O4 nanoparticles are successfully synthesized by a co-precipitation method
comprising Fe2+ and Fe3+ with ammonium hydroxide, NH4OH, and using citric acid as a surfactant. Comparative studies of Fe3O4 nanoparticles with and without surfactant are also carried out to examine their characteristics. Both types of synthesized
iron oxide nanoparticles are characterized by X-ray diffraction, X-ray photoelectron spectroscopy, field emission-scanning electron microscopy, transmission electron microscopy, and vibrating sample magnetometry. The images obtained by field emission-scanning electron microscopy show an average
diameter of 30 nm for citric acid-Fe3O4 nanoparticles. The Fourier transform infrared spectra indicate that the carboxylate groups of citric acid are bound onto the surface of magnetite nanoparticles by chemical bonds. For sensing experiments, the synthesized nanoparticles
are used to modify the glassy carbon electrode, and the resultant citric acid-Fe3O4 modified glassy carbon electrode is used for the detection of uric acid through cyclic voltammetry. In the case of the citric acid-Fe3O4 nanoparticles-modified glassy
carbon electrode, uric acid is oxidized at a less positive potential compared to oxidation using the naked Fe3O4 nanoparticles and a bare glassy carbon electrode. The citric acid-Fe3O4 nanoparticles-modified glassy carbon electrode exhibit a good
linear response range for the detection of uric acid of 7.5 μM-0.18 mM, with a lower detection limit of 7.5 μM uric acid. This excellent performance of the fabricated biosensor is attributed to the larger surface area availability of citric acid-Fe3O4
nanoparticles, which promotes constant electron transfer between the modified glassy carbon electrode and the biomolecules (uric acid). The improved electrocatalytic activity of this modified electrode clearly proves that the proposed method is promising for the development of other electrochemical
biosensors.