Potentiometric detection of hydrogen peroxide and apparatus therefor

• US 4,340,448 A
• Filed: 08/28/1978
• Issued: 07/20/1982
• Est. Priority Date: 08/28/1978
• Status: Expired due to Term

• Current Assignee: University Of Pittsburgh (University of Pittsburgh of The Commonwealth System of Higher Education)
• Original Assignee: University Of Pittsburgh (University of Pittsburgh of The Commonwealth System of Higher Education)
• Inventors: Liu, Chung-Chiun, Wingard, Lemuel B. Jr., Schiller, Julian G.
• Primary Examiner(s): Kaplan, G. L.
• Application Number:
  US05/937,365
• Time in Patent Office: 1,422 Days
• Field of Search: 204/195 B, 204/195 P, 204/1 E, 195/103.5 R, 195/103.5 C, 195/127, 128/2 E, 324/29, 435/291, 435/4, 435/14, 435/817
• US Class Current: 205/778
• CPC Class Codes: C12Q 1/005 involving specific analytes or enzymes including groups of enzymes, e.g. oxydases; C12Q1/004 takes precedence
• CPC Class Codes: C12Q 1/54 involving glucose or galactose
• CPC Class Codes: G01N 27/3271 Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood amperometry per se G01N27/49; aspects concerning the enzyme reagent C12Q1/001
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode

Abstract

A method for potentiometric detection of hydrogen peroxide including providing an electrolytic cell having a working electrode and a reference electrode. The working electrode is composed of a hydrogen peroxide sensitive material and also is employed as a support for an oxidase enzyme. Introducing a hydrogen peroxide releasing substance into the cell and releasing the hydrogen peroxide by effecting interaction with the enzyme. Developing in said cell an electrical potential which is a function of the concentration of the hydrogen peroxide and measuring the electrical potential of the cell. The method may be employed as a quantitative glucose detector by employing as the enzyme or enzymes glucose oxidase with or without catalase.

Apparatus for potentiometric determination of hydrogen peroxide includes a cell containing an electrolyte, a working electrode and a reference electrode. An electrometer is operatively associated with the electrodes. The working electrode is composed of a material which will create an electrical potential when it interacts with hydrogen peroxide. At least one oxidase enzyme is immobilized on the working electrode.

Claims

1. A method for potentiometric detection of hydrogen peroxide comprising

providing an electrolytic cell having a reference electrode and a working electrode composed at least in part of a hydrogen peroxide sensitive material,

immobilizing at least one oxidase enzyme on said working electrode,

said immobilized enzyme including catalase,

introducing a hydrogen peroxide releasing substance into said cell,

releasing said hydrogen peroxide by effecting contact between said enzyme and said hydrogen peroxide releasing substance,

developing in said cell through interaction between said hydrogen peroxide and said working electrode an electrical potential which is a function of the concentration of said hydrogen peroxide in said electrolytic cell,

maintaining the pH of said cell in the range of about 5 to 9, and

measuring said electrical potential of said cell whereby said working electrode will serve as a support for said oxidase enzyme and also as a hydrogen peroxide sensitive electrode to provide an electrical potential signal which is a function of the concentration of said hydrogen peroxide.

2. The method of claim 1 including

providing glucose in said hydrogen peroxide releasing substance,

reducing said glucose to gluconic acid and hydrogen peroxide, and

operating said cell at a pH of about 6.3 to 8.0.

3. The method of claim 1 including immobilizing at least one said oxidase enzyme selected from the group consisting of Superoxide dismutase, Nitroethane oxidase, D-aspartate oxidase, D-amino acid oxidase, L-amino acid oxidase, Amine oxidase, Pyridox amine phosphate oxidase, Amine oxidase, D-glutamate oxidase, Ethanolamine oxidase, Pyruvate oxidase, Oxalate oxidase, Glycollate oxidase, Glucose oxidase, Hexose oxidase, Cholesterol oxidase, Aryl alcohol oxidase, L-gulonolactone oxidase, Golactose oxidase, Pyranose oxidase, L-Sorbose oxidase, Pyridoxine 4-oxidase, Alcohol oxidase, L-2-hydroxyacid oxidase, Dehydro-oratate oxidase, Lathosterol oxidase, Sarcosine oxidase, N-Methylamino acid oxidase, N⁶ -Methyl lysine oxidase, 6-hydroxy-L-nicotine oxidase, 6-hydroxy-D-nicotine oxidase, Sulphite oxidase, 3-hydroxyanthranilate oxidase, Aldehyde oxidase, and Xanthine oxidase.

4. The method of claim 1 wherein said immobilized enzyme includes glucose oxidase.

5. The method of claim 1 including immobilizing said enzyme on said working electrode by providing said enzyme in a gel which is cast on said working electrode, whereby said working electrode will serve as both a support and a source of an electrical potential signal corresponding to hydrogen peroxide concentration.

6. The method of claim 5 including employing a gel which permits oxygen and glucose to diffuse therethrough.

7. The method of claim 1 including providing said working electrode of a platinum screen.

8. The method of claim 1 including reducing a portion of said hydrogen peroxide to oxygen and water by means of said catalase.

9. An apparatus for potentiometric detection of hydrogen peroxide comprising

a cell containing an electrolyte, a working electrode and a reference electrode,

an electrometer operatively associated with said working electrode and said reference electrode,

said working electrode composed of a material which creates an electrical potential when it interacts with hydrogen peroxide,

at least one oxidase enzyme immobilized on said working electrode,

said enzyme includes glucose oxidase and catalase,

whereby introduction of a hydrogen peroxide containing substance into said cell will result in said enzyme releasing hydrogen peroxide from said hydrogen peroxide releasing substance with the hydrogen peroxide interacting with said working electrode and said working electrode functioning as a support for said oxidase enzyme and to generate an electrical potential which is a function of the concentration of said hydrogen peroxide.

10. The apparatus of claim 9 wherein said working electrode is a platinum screen.

11. The apparatus of claim 9 including said enzymes being immobilized by being secured to said working electrode by a gel.

12. The apparatus of claim 9 including said enzymes including at least one enzyme selected from the group consisting of Superoxide dismutase, Nitroethane oxidase, D-aspartate oxidase, D-amino acid oxidase, L-amino acid oxidase, Amine oxidase, Pyridox amine phosphate oxidase, Amine oxidase, D-glutamate oxidase, Ethanolamine oxidase, Pyruvate oxidase, Oxalate oxidase, Glycollate oxidase, Glucose oxidase, Hexose oxidase, Cholesterol oxidase, Aryl alcohol oxidase, L-gulonolactone oxidase, Golactose oxidase, Pyranose oxidase, L-Sorbose oxidase, Pyridoxine 4-oxidase, Alcohol oxidase, L-2-hydroxyacid oxidase, Dehydro-oratate oxidase, Lathosterol oxidase, Sarcosine oxidase, N-Methylamino acid oxidase, N⁶ -Methyl lysine oxidase, 6-hydroxy-L-nicotine oxidase, 6-hydroxy-D-nicotine oxidase, Sulphite oxidase, 3-hydroxyanthranilate oxidase, Aldehyde oxidase, and Xanthine oxidase.

13. The apparatus of claim 9 including said electrolyte having a pH of about 5 to 9.