Direct electrochemistry and electrocatalysis of hemoglobin immobilized in a magnetic nanoparticles-chitosan film

Abstract

Magnetic nanoparticles (Fe3O4) were synthesized by a chemical coprecipitation method. X-ray diffraction (XRD) and transmission electron microscope (TEM) were used to confirm the crystallite structure and the particle's radius. The Fe3O4 nanoparticles and chitosan (CS) were mixed to form a matrix in which haemoglobin (Hb) can be immobilized for the fabrication of H2O2 biosensor. The Fe3O4–CS–Hb film exhibited a pair of well-defined and quasi-reversible cyclic voltammetric peaks due to the redox of Hb–heme Fe (III)/Fe (II) in a pH 7.0 phosphate buffer. The formal potential of Hb–heme Fe(III)/Fe(II) couple varied linearly with the increase of pH in the range of 4.0–10.0 with a slope of 46.5mVpH−1, indicating that electron transfer was accompanied with single proton transportation in the electrochemical reaction. The surface coverage of Hb immobilized on Fe3O4–CS film glassy carbon electrode was about 1.13×10−10molcm−2. The heterogeneous electron transfer rate constant (ks) was 1.04s−1, indicating great facilitation of the electron transfer between Hb and magnetic nanoparticles-chitosan modified electrode. The modified electrode showed excellent electrocatalytic activity toward oxygen and hydrogen peroxide reduction. The apparent Michaelis–Menten constant KMapp for H2O2 was estimated to be 38.1μmolL−1.