Analytical process and means for measuring the amount of hydrogen peroxide in aqueous media and of organic substrates generating hydrogen peroxide by enzymatic oxidation

• US 4,353,983 A
• Filed: 07/15/1980
• Issued: 10/12/1982
• Est. Priority Date: 11/15/1978
• Status: Expired due to Term

• Current Assignee: Schiapparelli Biosystems, Inc.
• Original Assignee: Battelle Memorial Institute
• Inventors: Siddiqi, Iqbal
• Primary Examiner(s): Wiseman, Thomas G.
• Application Number:
  US06/205,325
• Time in Patent Office: 819 Days
• Field of Search: 435/11, 435/14, 435/25, 435/28, 435/817, 204/1 T, 204/195 B, 204/195 R, 204/195 M, 23/230 B, 23/230 R, 424/2
• US Class Current: 205/777.5
• CPC Class Codes: C12Q 1/28 involving peroxidase
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode
• CPC Class Codes: Y10T 436/206664 Ozone or peroxide

Abstract

The present invention relates to the quantitative determination of hydrogen peroxide in water media and of substrates capable of being oxidized enzymatically with the formation of H₂ O₂ as well as the enzymes which are involved in such reaction and also the peroxidase which catalyzes the oxidation by H₂ O₂ of other substrates.

Claims

1. A method of quantatively determining a constituent selected from the group which consists of hydrogen peroxide and peroxidase in an aqueous sample, said method comprising the steps of:

(a) mixing said sample with a reaction system selectively containing a known amount of peroxidase or hydrogen peroxide, respectively, and in excess of an organic fluorine compound in the form of a fluoroaniline, a fluoroanisole or a fluorophenol having at least one C--F bond cleaving on a peroxidase catalyzed oxidation by hydrogen peroxide whereby F^- ions are formed in the system;

(b) exposing the reaction system to an F^- selective electrode; and

(c) electrochemically measuring by said electrode the rate of formation of F^- ions liberated by the peroxidase catalyzed cleavage of said C--F bond.

2. The method defined in claim 1 in which said sample is to be analyzed for hydrogen peroxide wherein said system is provided with a concentration of peroxidase sufficient to generate a rate of F^- formation for measurement over a limited period of time, and maintaining said concentration constant for a range of comparative analytical measurements.

3. The method defined in claim 2 wherein said reaction system is prepared by combining a buffer, said peroxidase and said fluorine compound and mixing said sample therewith, the rate of change of the potential of said electrode by measurement and the rate data thus obtained being compared with standardizing data with previous controlled analysis carried out identically on calibrating solutions of known hydrogen peroxide concentration.

4. The method defined in claim 1 wherein said sample contains peroxidase and said system is provided with sufficient hydrogen peroxide to maintain the concentration thereof substantially constant for the period in which the formation rate of F^- is measured.

5. The method defined in claim 1, 2, 3 or 4 wherein said organic fluorine compound is selected from the group which consists of p-fluoroaniline, p-fluorophenol, 2,3,5,6-tetrafluorophenol, 5-fluorophenol, 5-fluoro-2-methylaniline and p-fluoroanisole.

6. A method of quantitatively determining in an aqueous medium, an organic substrate sample, which comprises the steps of:

(a) preparing an aqueous reagent solution containing at least a buffer, a conjugate oxidase specific to said organic substrate and capable of oxidizing said organic substrate to yield H₂ O₂ as an oxidation product, a peroxidase, and an organic fluoro compound selected from the group of a fluoroaniline, a fluorophenol, and a fluoroanisole, the C--F bond of which is cleavable with quantitative liberation of F^- ion by peroxidase-catalyzed oxidation with the H₂ O₂ produced during the oxidase-catalyzed oxidation, the rate of the peroxidase-catalyzed oxidation being much greater than the rate of the oxidase-catalyzed oxidation, and the amount of the organic fluoro compound present being in excess of the rate limiting amount thereof for the peroxidase-catalyzed oxidation;

(b) mixing said aqueous reagent solution in excess of the rate limiting amount thereof for the oxidase-catalyzed oxidation with the organic substrate sample to be analyzed to oxidize the organic substrate to form hydrogen peroxide, said hydrogen peroxide then oxidizing the organic fluoro compound in the presence of the peroxidase to quantitatively split off F^- ion;

(c) measuring, in said mixture formed in step (b), with an F^- ion selective electrode the rate variation of the potential of said electrode with time during the peroxidase splitting reaction of said F^- ion;

(d) comparing said potential rate data thus obtained with standard rate potentials resulting from calibration analysis carried out previously on samples containing known concentrations of the same organic substrate being analyzed; and

(e) correlating the value measured in step (c) with the standard data corresponding to the known concentration of said substrate expressed in step (d) so as to determine the concentration of the organic substrate to be analyzed.

7. The method defined in claim 6, step (a) wherein the concentration of the conjugate oxidase is sufficient to enable the rate of H₂ O₂ formation to be measurable over a limited period of time and keeping said concentration constant from run to run for a full set of comparative analytical measurements.

8. The method defined in claim 6 wherein said organic substrate to be analyzed is glucose or cholesterol and wherein the conjugate oxidase is respectively glucose oxidase and cholesterol oxidase.

9. The method defined in claim 6, step (a), wherein the organic fluoro compound is selected from the group consisting of p-fluoroaniline, p-fluorophenol, 2,3,5,6-tetrafluorophenol, 5-fluorophenol, 5-fluoro-2-methyl-aniline and p-fluoro-anisole.

10. A method of quantitatively determining in an aqueous medium, a conjugate oxidase of an organic substrate, which comprises the steps of:

(a) preparing an aqueous reagent containing at least a buffer, a peroxidase, an organic substrate for which the conjugate oxidase is specific, said organic substrate being capable of oxidation by said conjugate oxidase to yield H₂ O₂ and said organic substrate being present in excess of the rate limiting amount for the oxidase-catalyzed oxidation, and an organic fluoro compound selected from the group consisting of a fluoroaniline, a fluorophenol, and a fluoroanisole, the C--F bond of which is cleavable with quantitative liberation of F^- ion by peroxidase-catalyzed oxidation with the H₂ O₂ produced during the oxidase-catlyzed oxidation, the rate of the peroxidase-catalyzed oxidation being much faster than the rate of the oxidase-catalyzed oxidation, and the amount of the organic fluoro compound present being in excess of the rate limiting amount for the peroxidase-catalyzed oxidation;

(b) immersing in said aqueous reagent solution an F^- selective electrode;

(c) mixing said aqueous reagent solution with a sample containing the conjugate oxidase to be analyzed in order to oxidize the organic substrate to form hydrogen peroxide, said hydrogen peroxide then oxidizing the organic fluoro compound in the presence of the peroxidase to quantitatively split off F^- ion, and measuring the variation of the potential of said F^- selective electrode with time in response to change in the [F^- ]; and

(d) comparing said potential rate data thus obtained, or the corresponding [F^- ] data collected from the Nernst equation, with standard rate potentials, or corresponding standard [F^- ] data, resulting from calibration analysis carried out earlier on samples containing known concentrations of the conjugate oxidase to be analyzed, and correlating said values measured during step (c) with said standard data to obtain the desired results.

11. The method defined in claim 10, step (a), wherein the organic substrate is present in excess of the rate limiting amount for the oxidase-catalyzed oxidation to the extent that its concentration will remain approximately constant during the period when the rate of the hydrogen peroxide formation is measured.

12. The method defined in claim 10 wherein the conjugate oxidase to be analyzed is glucose oxidase or cholesterol oxidase and wherein the respective organic substrate is glucose or cholesterol.

13. The method defined in claim 10, step (a), wherein the organic fluoro compound is selected from the group consisting of p-fluoroaniline, p-fluorophenol, 2,3,5,6-tetrafluorophenol, 5-fluorophenol, 5-fluoro-2-methyl-aniline and p-fluoro-anisole.