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

Abstract Magnetic nanoparticles (Fe 3 O 4 ) 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 Fe 3 O 4 nanoparticles and chitosan (CS) were mixed to form a matrix in which haemoglobin (Hb) can be immobilized for the fabrication of H 2 O 2 biosensor. The Fe 3 O 4 –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 46.5 mV pH −1 , indicating that electron transfer was accompanied with single proton transportation in the electrochemical reaction. The surface coverage of Hb immobilized on Fe 3 O 4 –CS film glassy carbon electrode was about 1.13 × 10 −10  mol cm −2 . The heterogeneous electron transfer rate constant ( k s ) was 1.04 s −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 K M app for H 2 O 2 was estimated to be 38.1 μmol L −1 .