doi:10.1016/j.bios.2008.08.017
Copyright © 2008 Elsevier B.V. All rights reserved.
Polyazetidine-based immobilization of redox proteins for electron-transfer-based biosensors
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Marco Frasconia, Gabriele Faveroa, Massimo Di Fuscoa and Franco Mazzei
, a, 
aUniversità degli Studi di Roma “La Sapienza”, Dipartimento di Chimica e Tecnologie del Farmaco, Piazzale Aldo Moro 5, 00185 Rome, Italy
Received 4 June 2008;
revised 28 July 2008;
accepted 11 August 2008.
Available online 22 August 2008.
Abstract
A highly stable functional composite film was prepared using polyazetidine prepolymer (PAP) with peroxidase from horseradish (HRP) and/or glucose oxidase (GOx). The good permeability of the PAP layer to classical electrochemical mediators, as evaluated by the determination of the diffusion coefficient of different redox molecules, is of great importance in view of the use of PAP as an immobilizing agent in second-generation biosensor development.
Cyclic voltammetry of the HRP–PAP layer on a glassy carbon electrode (GCE) showed a pair of stable and quasi-reversible peaks for the HRP–Fe(III)/Fe(II) redox couple at about −370 mV vs. Ag/AgCl electrode in pH 6.5 phosphate buffer. The electrochemical reaction of HRP entrapped in the PAP film exhibited a surface-controlled electrode process. This film and the successive modifications (HRP–PAP self-assembled monolayer (SAM) modified Au electrode) were used as a biological catalyst (hydrogen peroxide transducers) for glucose biosensors, after coupling to GOx. Both HRP/GOx–PAP and HRP/GOx–PAP SAM third generation biosensors were prepared and characterized.
The use of PAP as immobilizing agent offers a biocompatible micro-environment for confining the enzyme and foreshadows the great potentiality of this immobilizing agent not only in theoretical studies on protein direct electron transfer but also from an applications point of view in the development of second- and third-generation biosensors.
Keywords: Immobilization; Electrochemical biosensor; Electron transfer
Fig. 1. Cyclic voltammograms of GOx–PAP immobilized on GCE, carried out in PB at 5 mV/s in presence of 1 mM FCA containing different concentrations of glucose; in the inset, the limiting current vs. glucose concentration is reported.
Fig. 2. Cyclic voltammograms of HRP–PAP immobilized on GCE in 0.1 M PB (pH 6.5): (a) carried out at different scan rates (from 15 to 500 mV/s); in the inset, the anodic and cathodic peak currents vs. scan rate is reported; (b) carried out at 200 mV/s scan rate, in presence of (a.) 0.4, (b.) 0.8 and (c.) 1.2 mmol/L H2O2 (dashed line refers to blank); in the inset, the signals obtained after blank subtraction is shown.
Fig. 3. Cyclic voltammograms of HRP–PAP immobilized on (a) GCE and different SAM covered electrodes: (b) MPA–AuE and (c) NTP–AuE, carried out in 0.1 M PB at pH 6.5 (scan rate 25 mV/s).
Scheme 1. PAP structure and typical reactions.
Table 1.
Electrochemical parameters for HRP–PAP biosensors compared to those obtained for HRP–PAP SAM-based biosensors

Measurements were carried out in PB 0.1 M (pH 6.5) and they are the mean values of at least 10 determinations.
Table 2.
Kinetic and analytical parameters for HRP–PAP biosensors, H2O2 as substrate compared to those obtained for HRP–PAP SAM-based biosensors

Measurements were carried out in PB 0.1 M (pH 6.5) and they are the mean values of at least 10 determinations.
Table 3.
Analytical parameters for HRP/GOx–PAP and HRP/GOx–PAP SAM-based biosensors, glucose as substrate

Measurements were carried out in PB 0.1 M (pH 6.5) and they are the mean values of at least 10 determinations.

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