Assay of peroxidatively active materials

• US 4,269,938 A
• Filed: 03/08/1979
• Issued: 05/26/1981
• Est. Priority Date: 03/08/1979
• Status: Expired due to Term

• Current Assignee: Clinical Diagnostic Systems Inc.
• Original Assignee: Eastman Kodak Company
• Inventors: Frank, David S.
• Primary Examiner(s): Gron, Teddy S.
• Application Number:
  US06/018,532
• Time in Patent Office: 810 Days
• Field of Search: 435/7, 435/14, 435/28, 435/188, 252/408, 252/186, 252/188.3 CL, 252/301.16, 424/7, 424/8, 424/12, 23/230 B, 422/61, 422/56, 422/57, 422/55
• US Class Current: 435/7.9
• CPC Class Codes: C12Q 1/28 involving peroxidase
• CPC Class Codes: C12Q 2326/40 Triphenylmethane dye chromogens, e.g. fluorescein derivatives
• CPC Class Codes: G01N 33/535 with enzyme label or co-enzymes, co-factors, enzyme inhibitors or enzyme substrates
• CPC Class Codes: Y10S 435/97 Test strip or test slide
• CPC Class Codes: Y10T 436/144444 Glucose
• CPC Class Codes: Y10T 436/148888 Uric acid

Abstract

A new peroxidase assay for substances demonstrating peroxidative activity is described which is based on the peroxidase catalyzed oxidation of dichlorofluorescin to dichlorofluorescein by peroxide. The dichlorofluorescin is formed from diacetyldichlorofluorescin either by the direct addition of peroxide or by the inclusion of a peroxide generating system (e.g., glucose plus glucose oxidase or uric acid and uricase) in the reaction mixture. As long as all reactants other than the peroxidase are present in excess, the rate of fluorescence increase is linearly related to the amount of peroxidase in the sample under assay.

Claims

1. A composition useful for the determination of a substance having peroxidative activity, said composition, consisting essentially of diacetyldichlorofluorescin and a source of hydrogen peroxide in a concentration of from about 10^-6 to 10^-2 M, the ratio of diacetyldichlorofluorescin to hydrogen peroxide or generated hydrogen peroxide ranging from 1:

5 to 1;

100.

2. The composition of claim 1 wherein said source of hydrogen peroxide comprises an enzyme and an enzyme substrate which, when contacted in an aqueous medium in the presence of oxygen, release hydrogen peroxide.

3. The composition of claim 1 wherein said source of hydrogen peroxide is hydrogen peroxide.

4. The composition of claim 1 wherein said source of hydrogen peroxide is urea peroxide.

5. The composition of claim 2 wherein said enzyme is an oxidative enzyme and said substrate is the corresponding substrate for said oxidative enzyme.

6. The composition of claim 2 wherein said enzyme is glucose oxidase and said substrate is glucose.

7. The composition of claim 2 wherein said enzyme is uricase and said substrate is uric acid.

8. The composition of claim 2 wherein said enzyme is cholesterol oxidase and said substrate is cholesterol.

9. The composition of claim 1 further including a buffer which maintains the pH of the composition at a pH of between about 7 and 9.

10. The composition of claim 1 wherein the concentration of diacetyldichlorofluorescin is from about 10^-7 to 10^-3 M.

11. A method for assaying peroxidase comprising the steps of

(a) contacting in an aqueous medium a sample for analysis and a composition consisting essentially of diacetyldichlorofluorescin and a source of hydrogen peroxide in a concentration from about 10^-6 to 10^-2 M to produce dichlorofluorescein, the ratio of diacetyldichlorofluorescin to hydrogen peroxide or generated hydrogen peroxide ranging from 1:

5 to 1;

100; and

(b) detecting the dichlorofluorescein.

12. The method of claim 11 wherein the dichlorofluorescein is detected by fluorescence rate measurements.

13. The method of claim 11 wherein said source of hydrogen peroxide comprises an enzyme and an enzyme substrate which, when contacted in an aqueous medium in the presence of oxygen, release hydrogen peroxide.

14. The method of claim 11 wherein said source of hydrogen peroxide is hydrogen peroxide.

15. The method of claim 11 wherein said source of hydrogen peroxide is urea peroxide.

16. The method of claim 13 wherein said enzyme is an oxidative enzyme and said substrate is the corresponding substrate for said oxidative enzyme.

17. The method of claim 11 wherein the concentration of diacetyldichlorofluorescin in said composition is from about 10^-7 to about 10^-3 M.

18. The method of claim 11 wherein said composition further includes a buffer which maintains the pH of the composition at a pH of between about 7 and 9.

19. A method for assaying peroxidase comprising the steps of

(a) contacting a substantially dry element comprising a reagent having a composition consisting essentially of diacetyldichlorofluorescin and a dry source of hydrogen peroxide at a concentration of from about 10^-6 to 10^-2 M with a sample for analysis, the ratio of diacetyldichlorofluorescin to generated hydrogen peroxide ranging from 1:

5 to 1;

100; and

(b) detecting the dichlorofluorescein resulting from said contact.

20. The method of claim 19 wherein the dichlorofluorescein is detected by fluorescence rate measurements.

21. The method of claim 19 wherein said source of hydrogen peroxide comprises an enzyme and an enzyme substrate which, when contacted in an aqueous medium in the presence of oxygen, release hydrogen peroxide.

22. The method of claim 19 wherein said source of hydrogen peroxide is urea peroxide.

23. A dry test element for the assay of peroxidase in an aqueous liquid, said element having a reagent zone containing an assay composition for peroxidase, said assay composition consisting essentially of diacetyldichlorofluorescin and a dry source of hydrogen peroxide at a concentration of from about 10^-6 to 10^-2 M, the ratio of diacetyldichlorofluorescin to generated hydrogen peroxide ranging from 1:

5 to 1;

100.

24. The element of claim 23 wherein said source of hydrogen peroxide comprises an enzyme and an enzyme substrate which, when contacted in an aqueous medium in the presence of oxygen, release hydrogen peroxide.

25. The element of claim 23 wherein said source of hydrogen peroxide is urea peroxide.

26. The element of claim 23 wherein said enzyme is an oxidative enzyme and said substrate is the corresponding substrate for said oxidative enzyme.

27. An element for the detection of peroxidase comprising fibrous material which is impregnated with a reagent consisting essentially of diacetyldichlorofluorescin and a source of hydrogen peroxide at a concentration of from about 10^-6 to 10^-2 M, the ratio of diacetyldichlorofluorescin to hydrogen peroxide or generated hydrogen peroxide ranging from 1:

5 to 1;

100.

28. The element of claim 27 wherein said fibrous material is paper.

29. The element of claim 27 wherein said source of hydrogen peroxide is hydrogen peroxide.

30. The element of claim 27 wherein said source of hydrogen peroxide is urea peroxide.

31. The element of claim 27 wherein said source of hydrogen peroxide comprises an enzyme and an enzyme substrate which, when contacted in an aqueous medium in the presence of oxygen, release hydrogen peroxide.

32. An element for the detection of peroxidase comprising a spreading layer and a reagent layer in fluid contact under conditions of use, said reagent layer comprising a reagent consisting essentially of diacetyldichlorofluorescin and a dry source of hydrogen peroxide at a concentration of from about 10^-6 to 10^-2 M, the ratio of diacetyldichlorofluorescin to generated hydrogen peroxide ranging from 1:

5 to 1;

100.

33. The element of claim 32 wherein said source of hydrogen peroxide comprises an enzyme and an enzyme substrate which, when contacted in an aqueous medium in the presence of oxygen, release hydrogen peroxide.

34. The element of claim 32 wherein said source of hydrogen peroxide is urea peroxide.

35. The element of claim 33 wherein said enzyme is an oxidative enzyme and said substrate is the corresponding substrate for said oxidative enzyme.

36. An element for the detection of peroxidase in a liquid, the element comprising a spreading layer, a reagent layer and a registration layer all in fluid contact under conditions of use and a support, the reagent layer intervening the spreading layer and the registration layer intervening the reagent layer and the support, the reagent layer comprising a reagent consisting essentially of diacetyldichlorofluorescin and a dry source of hydrogen peroxide at a concentration of from about 10^-6 to 10^-2 M, the ratio of diacetyldichlorofluorescin to generated hydrogen peroxide ranging from 1:

5 to 1;

100.

37. The element of claim 36 wherein said source of hydrogen peroxide comprises an enzyme and an enzyme substrate which, when contacted in an aqueous medium in the presence of oxygen, release hydrogen peroxide.

38. The element of claim 36 wherein said source of hydrogen peroxide is urea peroxide.

39. The element of claim 37 wherein said enzyme is an oxidative enzyme and said substrate is the corresponding substrate for said oxidative enzyme.

40. The element of claim 36 wherein said reagent layer further comprises a buffer which maintains the pH of the reagent at a pH of between about 7 and 9.

41. A method of assaying for antigen or antibody present in a sample to be tested comprising:

(a) labeling a known amount of antigen or antibody with peroxidase and adding said labeled antigen or antibody with said sample to be tested to a known amount of corresponding antigen or antibody; and

(b) determining the amount of unknown antigen or antibody by

(i) contacting in an aqueous medium the mixture of (a) and a composition consisting essentially of diacetyldichlorofluorescin and a source of hydrogen peroxide at a concentration of from about 10^-6 to 10^-2 M to produce dichlorofluorescein, the ratio of diacetyldichlorofluorescin to hydrogen peroxide or generated hydrogen peroxide ranging from 1;

5 to 1;

00;

(ii) detecting the dichlorofluorescein.