Method and reagent for the assay of hydroperoxide

• US 4,143,080 A
• Filed: 11/11/1977
• Issued: 03/06/1979
• Est. Priority Date: 11/25/1976
• Status: Expired due to Term

• Current Assignee: Goodyear Tire & Rubber Company
• Original Assignee: Goodyear Tire & Rubber Company
• Inventors: Harders, Hans-Dieter, Helger, Roland
• Primary Examiner(s): Wolk, Morris O.
• Assistant Examiner(s): Turk, Arnold
• Application Number:
  US05/850,523
• Time in Patent Office: 480 Days
• Field of Search: 23/230 B, 195/103.5 R, 195/103.5 C, 252/408
• US Class Current: 436/66
• CPC Class Codes: C12Q 1/28 involving peroxidase
• CPC Class Codes: C12Q 1/54 involving glucose or galactose
• CPC Class Codes: C12Q 1/60 involving cholesterol
• CPC Class Codes: Y10S 436/904 Oxidation - reduction indicators

Abstract

In a method for detection and/or assay of hydroperoxides (or, indirectly, of substances, such as cholesterol or glucose, which react to liberate hydroperoxides) using an assay reagent comprising a water-soluble iodide, a redox catalyst and a stabilizer, an improvement is provided wherein when the determination is made in the presence of protein, the redox catalyst concentration in the reagent is 5-500 μM and the stabilizer concentration in the reagent is 5-100 mg/l. A corresponding improvement in the assay reagent is also provided.

Claims

1. In a process for the photometric determination of hydroperoxides per se in a protein-containing body fluid, or indirectly of substances therein which react to liberate hydroperoxides, using an assay reagent comprising a water-soluble iodide, a redox catalyst and stabilizer, the improvement wherein the concentration of the redox catalyst in the reagent is 5-500 μ

M, and the concentration of stabilizer is 5-100 mg/l whereby the body fluid does not require deproteinization before the photometric determination.

2. The improvement of claim 1, wherein the redox catalyst is a molybdate, tungstate or vanadate.

3. The improvement of claim 2, wherein 5-50 μ

M of ammonium molybdate is the redox catalyst.

4. The improvement of claim 1, wherein sodium azide, hexamethylenetetramine, potassium fluoride, potassium thiocyanate, ethylenediaminetetraacetic acid, nitrilotriacetic acid or a mixture thereof is the stabilizer.

5. In a process for the photometric determination in a protein-containing body fluid of hydrogen peroxide liberated from cholesterol treated with cholesterol oxidase, using an assay reagent comprising a water-soluble iodide, a redox catalyst and stabilizer, the improvement wherein the concentration of the redox catalyst in the reagent is 5-500 μ

M, and the concentration of stabilizer is 5-100 mg/l whereby the body fluid does not require deproteinization before the photometric determination.

6. The improved process of claim 5, wherein the determination is carried out in the presence of polyethylene glycol mono-(1,1,3,3-tetramethylbutyl)-phenyl ether and alkyldimethylbenzylammonium chloride.

7. In a reagent for the photometric determination of hydroperoxides per se or indirectly of substances which react to liberate hydroperoxides, comprising a water-soluble iodide, a redox catalyst and stabilizer, the improvement wherein the concentration of redox catalyst is 5-500 μ

M and the concentration of stabilizer is 5-100 mg/l.

8. The improvement of claim 7, wherein the redox catalyst is 5-50 μ

M of ammonium molydbate, the stabilizer is 10 mg/l of sodium azide and the soluble iodide is potassium iodide.

9. A method of detecting and assaying hydroperoxide in the presence of protein which comprises photometrically measuring the amount of triiodide ion formed when a reagent comprising water-soluble iodide, a redox catalyst in a concentration of 5-500 μ

M and stabilizer in a concentration of 5-100 mg/l is mixed with a protein- and hydroperoxide-containing test specimen.