Amperometric-non-enzymatic method of determining sugars and other polyhydroxy compounds

• US 4,127,448 A
• Filed: 02/28/1977
• Issued: 11/28/1978
• Est. Priority Date: 02/28/1977
• Status: Expired due to Term

• Current Assignee: First Wisconsin National Bank Of Milwaukee
• Original Assignee: Calvin O. Huber, Karl G. Schick
• Inventors: Schick, Karl G., Huber, Calvin O.
• Primary Examiner(s): Tung, T.
• Application Number:
  US05/772,454
• Time in Patent Office: 638 Days
• Field of Search: 284/1 TK, 284/195 R
• US Class Current: 205/777.5
• CPC Class Codes: G01N 27/3273 Devices therefor, e.g. test element readers, circuitry details not specific to biochemical electrodes G01N33/4875

Abstract

A method for determining hydrogen peroxide, sugars and other polyhydroxy compounds in blood serum, urine and aqueous solutions by direct electrochemical oxidation in aqueous alkaline medium with a transition metal oxide catalyst electrode in the presence of lithium hydroxide in solution.

Claims

1. A method for determination of hydrogen peroxide, sugars and other polyhydroxy compounds comprising providing the compound in an aqueous alkaline solution, applying a constant potential between a transition metal oxide catalyst electrode and a counter electrode immersed in the solution whereby electrocatalytic oxidation of the hydroxy compound occurs at the surface of the transition metal oxide electrode, and measuring the rise in current from the electrochemical oxidation.

2. The method as claimed in claim 1 in which the solution has a pH within the range of 10 to 14.

3. The method as claimed in claim 1 in which lithium hydroxide is present in the dissolved state in the solution.

4. The method as claimed in claim 1 in which the solution contains ions of the transition metal of the oxide catalyst electrode.

5. The method as claimed in claim 1 in which the oxide electrode is covered with a microporous membrane to keep proteins and high molecular weight molecules from interfering with the determination.

6. The method as claimed in claim 1 in which the solution contains the material to be determined in a concentration within the range of 1 ×

10^-7 to 1 ×

10^-2 M.

7. The method as claimed in claim 1 in which, when the polyhydroxy compound is serum glucose, the oxide electrode is protected with a microporous membrane and the solution has a pH within the range of 11 to 13, with lithium hydroxide and ions of the metal of the electrode present in low concentration in the solution.

8. The method as claimed in claim 1, in which, in the determination of serum triglyceride, the polyhydroxy compound is glycerol derived by hydrolyzation of the serum triglyceride to glycerol and fatty acid.

9. The method as claimed in claim 8 in which the hydrolyzation is carried out by reacting the serum triglyceride with the enzymes lipase and α

-chymotrypsin.

10. The method as claimed in claim 9 in which the reaction is carried out by incubation.

11. The method as claimed in claim 1 in which, in the determination of cholesterol in blood, the polyhydroxy compound is hydrogen peroxide derived by reacting the serum cholesterol with cholesterol ester hydrolase to convert cholesterol esters to free cholesterol and reacting the free cholesterol with cholesterol oxidase to yield hydrogen peroxide.

12. The method as claimed in claim 1 in which, in the determination of sugar in urine, the urine is first reacted with urease and uricase to deactivate uric acid.

13. The method as claimed in claim 12 in which the determination of sugar in urine is made both before and after reaction of the urine with urease and uricase whereby the difference in current levels indicates the amount of sugar in the urine.

14. The method as claimed in claim 1 in which the transition metal oxide is the oxide of the metal selected from the group consisting of manganese, copper, nickel, cobalt and siver.

15. The method as claimed in claim 1 in which the current rise is compared with the current rise of a known standard solution of hydroxy compound.