University of North Florida
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Contact Info

Stuart Chalk, Ph.D.
Department of Chemistry
University of North Florida
Phone: 1-904-620-1938
Fax: 1-904-620-3535
Email: schalk@unf.edu
Website: @unf

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J. Justin Gooding

Abbrev:
Gooding, J.J.
Other Names:
Address:
School of Chemical Sciences, The University of New South Wales, Sydney, NSW 2052, Australiab Intelligent Polymer Research Institute, University of Wollongong, NSW 2522, Australia
Phone:
+61-2-9385-5384
Fax:
+61-2-9285-6141

Citations 2

"Electrochemical Modulation Of Antigen-antibody Binding"
Biosens. Bioelectron. 2004 Volume 20, Issue 2 Pages 260-268
J. Justin Gooding, Christine Wasiowych, Donald Barnett, D. Brynn Hibbert, Joseph N. Barisci and Gordon G. Wallace

Abstract: The label-free amperometric detection of a rabbit IgG antigen by an anti-rabbit IgG antibody is achieved by observing the electrochemistry at a glassy carbon electrode modified with antibody entrapped in an electrodeposited polypyrrole membrane. In a flow injection apparatus the electrode is pulsed between -0.2 and +0.4 V versus Ag/AgCl. The pulsing of the electrode switches the polypyrrole membrane between the oxidized and reduced states. When antigen is injected into the flow stream a change in current is observed at the electrode despite the antigen or antibody being redox inactive at the potentials employed. It is proposed that this current is due to a change in the flux of ions into and out of the polypyrrole matrix during a pulse when the poly-anionic antigen is present. The immunoreaction was reversible because the 200 ms pulse at each potential was too short to allow secondary bonding forces (hydrogen bonding and hydrophobic forces) which are responsible for the strength of the antibody-antigen complex to be established. The consequence of the reversibility of the antigen-antibody binding is a low apparent affinity constant but an easily regenerated recognition interface.

"A Sulfite Biosensor Fabricated Using Electrodeposited Polytyramine: Application To Wine Analysis"
Analyst 1999 Volume 124, Issue 12 Pages 1775-1779
Manihar Situmorang, D. Brynn Hibbert, J. Justin Gooding and Donald Barnett

Abstract: The development of a sulfite biosensor based on the immobilization of sulfite oxidase (SOD) in electrodeposited polytyramine is described. Electropolymerization of polytyramine and simultaneous immobilization of SOD on platinized glassy carbon (GC/Pt) were performed in an aqueous solution of 0.1 M tyramine containing SOD. The sulfite biosensor constructed with five voltammetric sweep cycles showed a sensitive response to sulfite with a linear calibration curve in the concentration range 0.002-0.3 mM sulfite, slope 2.70 µA l mmol-1, and detection limit 0.001 mM sulfite (S/N = 3). Deposited polytyramine enhanced the selectivity of the biosensor by eliminating direct oxidation of sulfite and other interfering agents at the electrode. The biosensor was applied for the determination of sulfite in various types of wine samples, and the results obtained are in agreement with those using an AOAC method.