New glucose biosensor based on a poly(o-phenylendiamine)/glucose oxidase-glutaraldehyde/Prussian blue/Au electrode with QCM monitoring of various electrode-surface modifications

The immobilization of glucose oxidase (GOD) via its dip-dry coating on a Prussian blue (PB) modified An electrode followed by deposition of an outer poly(o-phenylenediamine) (PoPD) film and then glutaraldehyde (GA) cross-linking was investigated for amperometric glucose sensing, based on the reduction of enzymatically generated H2O2 catalyzed by the electroactive PB layer of the PoPD/GOD-GA/PB/Au electrode. The quartz crystal microbalance (QCM) was used to monitor various electrode-modification processes, and the effective enzymatic specific activity (ESA, defined as enzymatic activity per gram of enzyme) of immobilized GOD was estimated based on the mass of immobilized GOD (from QCM) and the quantity of hydrogen peroxide as the product of the enzymatic reaction (from amperometric detection) for the first time. The ESA of native GOD under our experimental conditions was also estimated via amperometric detection of enzymatically generated H2O2 at a PB-modified An electrode. Effects of various experimental parameters on glucose sensing, including the applied potential, solution pH and electroactive interferents, were investigated. At an optimal potential of -0.05 V versus saturated KCl calomel electrode (SCE), the current response of the biosensor in the selected phosphate buffer (pH 7.0) was linear with glucose concentration from 0.05 to 10 mmol L-1, with detection limit of 8 mu mol L-1, short response time (within similar to 5 s) and good anti-interferent ability. The Michaelis constant (K-m(app)) of the immobilized GOD was estimated as 19.6 mmol L-1. The biosensor exhibited good storage stability, i.e., 88% of its initial response was retained after 30-day storage in pH 7.0 phosphate buffer at 4 degrees C. Since the present sensor-fabrication platform is rather general and advantageous in saving biochemical reagents, it is recommended for the development of other biosensors based on other substrate electrode materials, e.g. glassy carbon that has been tested in this work with satisfactory results. (c) 2005 Elsevier B.V. All rights reserved.