5-methylphenazonium methylsulphate, (commonly named phenazine methosulphate, PMS) mediated electroxidation of ?-nicotinamide adenine dinucleotide (phosphate), reduced form, (NAD(P)H), on platinum, gold and carbon electrodes has been studied by electropolymerization of 1,2-, 1,3-, 1,4-diaminobenzene (DAB), pyrrole-2-carboxylic acid (PY-2-COOH) and 4,4'-dihydroxybenzophenone (DHB) in presence of PMS using cyclic voltammetry. The electroxidation of ascorbic acid has been evaluated on the electrodes elctropolymerized in absence and in presence of PMS. The same experiments have been carried out with NAD(P)H in solution. Results showed that the NAD(P)H is oxidized by PMS coimmobilized with the polymer film on the electrode surface. NAD(P)H has been measured in the range 10-6 - 10-2 mol 1-1 with a detection limit of 5 x 10-7 mol 1-1. Amperometric measurements of NAD(P)H have been carried out at -0.10 V and the efficiency of different electrodes based on different materials has been studied. The electropolymerization has been also carried out in presence of PMS and selected dehydrogenase enzymes. The activity of these enzymes has been tested amperometrically at 0.1 V. Enzyme substrates such as glucose, lactate and glutamate have been measured in the range 5 x 10-6 - 1 x 10-2 mol 1-1 with a detection limit 1 x 10-6 mol 1-1. Also the stability of these probes during time has been evaluated.

Enzyme electrode probes obtained by electropolymerization of monomers with PMS and selected dehydrogenase enzymes

Curulli A;
1997

Abstract

5-methylphenazonium methylsulphate, (commonly named phenazine methosulphate, PMS) mediated electroxidation of ?-nicotinamide adenine dinucleotide (phosphate), reduced form, (NAD(P)H), on platinum, gold and carbon electrodes has been studied by electropolymerization of 1,2-, 1,3-, 1,4-diaminobenzene (DAB), pyrrole-2-carboxylic acid (PY-2-COOH) and 4,4'-dihydroxybenzophenone (DHB) in presence of PMS using cyclic voltammetry. The electroxidation of ascorbic acid has been evaluated on the electrodes elctropolymerized in absence and in presence of PMS. The same experiments have been carried out with NAD(P)H in solution. Results showed that the NAD(P)H is oxidized by PMS coimmobilized with the polymer film on the electrode surface. NAD(P)H has been measured in the range 10-6 - 10-2 mol 1-1 with a detection limit of 5 x 10-7 mol 1-1. Amperometric measurements of NAD(P)H have been carried out at -0.10 V and the efficiency of different electrodes based on different materials has been studied. The electropolymerization has been also carried out in presence of PMS and selected dehydrogenase enzymes. The activity of these enzymes has been tested amperometrically at 0.1 V. Enzyme substrates such as glucose, lactate and glutamate have been measured in the range 5 x 10-6 - 1 x 10-2 mol 1-1 with a detection limit 1 x 10-6 mol 1-1. Also the stability of these probes during time has been evaluated.
1997
Dehydrogenase enzymes; Electrochemical biosensors; Electropolymerization; Interferences
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/125396
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