Assay device and method using a signal-modulating compound

• US 5,156,954 A
• Filed: 03/08/1989
• Issued: 10/20/1992
• Est. Priority Date: 03/08/1989
• Status: Expired due to Term

• Current Assignee: Cholestech Corporation (Abbott Laboratories)
• Original Assignee: Cholestech Corporation (Abbott Laboratories)
• Inventors: Mielke, Steven T., Hewett, Gary E.
• Primary Examiner(s): Robinson, Douglas W.
• Assistant Examiner(s): REARDON, TIMOTHY
• Application Number:
  US07/320,414
• Time in Patent Office: 1,322 Days
• Field of Search: 435/7.71, 435/7.72, 435/7.93, 435/11, 435/18, 435/19, 435/20, 435/21, 435/25, 435/28
• US Class Current: 435/18
• CPC Class Codes: C12Q 1/60 involving cholesterol
• CPC Class Codes: G01N 33/525 Multi-layer analytical elements

Abstract

An assay device and method for determining the concentration of an analyte. Analyte introduced by liquid absorption into the matrix is used to generate H2O2, via an analyte-specific oxidase, and the H₂ O₂ is utilized by peroxidase in the presence of peroxidase to convert a substrate reagent to a colored reaction product. A trapping compound in the matrix competes with the substrate reagent, in the presence of the peroxidase enzyme, to produce a silent reaction product, thus proportionately reducing the amount of signal reaction product generated by a given amount of analyte. Detection of a wider range of analyte concentrations is therefore possible.

Claims

1. An assay test strip for use in assaying the concentration of an analyte in an aqueous fluid sample, where the analyte is one which can serve as a substrate for an oxidase enzyme, with the generation of H₂ O₂ comprising:

(a) an absorbent matrix effective to absorb a volume of said sample;

(b) analyte-reaction reagents embedded in the matrix, including (i) an analyte-specific oxidase enzyme effective to react with analyte present in such a sample to produce H₂ O₂ ;

(ii) a peroxidase enzyme;

(iii) a primary substrate which can be converted from a reduced to an oxidized form by the peroxidase enzyme in the presence of H₂ O₂, and (iv) a secondary substrate capable of reacting with the oxidized form of the primary substrate to form an analyte-dependent amount of a colored reaction product, and

(c) a trapping compound embedded in the matrix, which trapping compound is effective to (i) compete with the secondary substrate for reaction with the oxidized form of the primary substrate to produce a substantially colorless product, and (ii) reduce the amount of colored reaction product generated by a given amount of analyte in proportion to the relative amounts of trapping compound and secondary substrate present in the matrix.

2. The test strip of claim 1, wherein the trapping compound is present in the matrix in an amount, relative to the amount of secondary substrate present in the matrix, which is effective to reduce the analyte-dependent amount of said colored reaction product to about 10-70% of the amount of colored reaction product formed in the absence of the trapping compound.

3. The test strip of claim 1, wherein said primary substrate is 4-amino antipyrine, and said trapping compound is a benzenediol.

4. The test strip of claim 3, wherein said secondary substrate is N-ethyl-N-sulfohydroxy propyl-m-toluidine and said trapping compound is selected from the group consisting of 1,3-benzenediol and 1,4-benzenediol, at a concentration of trapping compound substantially in the range between 0.5 mM and 2 mM.

5. The test strip of claim 2, for use in assaying serum cholesterol, wherein said analyte-reaction reagents further include cholesterol esterase, and said oxidase enzyme is cholesterol oxidase.

6. The test strip of claim 2, for use in assaying serum triglycerides, wherein said analyte-reaction reagents includes lipase, a source of ATP, and glycerol kinase, and said oxidase enzyme is glycerol-phosphate oxidase.

7. An assay test strip for use in assaying the concentration of an analyte in a blood sample, where the analyte is one which can serve as a substrate for an oxidase enzyme, with the generation of H₂ O₂ comprising:

(a) an absorbent matrix effective to absorb a volume of said sample;

(b) analyte-reaction reagents embedded in the matrix, including (i) an analyte-specific oxidase enzyme effective to react with analyte present in such a sample to produce H₂ O₂ ;

(ii) 4-amino antipyrine and a peroxidase effective to oxidize the 4-amino antipyrine inthe presence of H₂ O₂ ; and

(iii) a secondary substrate effective to react with the oxidized 4-amino antipyrine to produce an analyte-dependent amount of a colored reaction product; and

(c) embedded in the matrix, a trapping compound which is effective to (i) compete with the secondary substrate for reaction with the oxidized 4-amino antipyrine to produce a substantially colorless product, and (ii) reduce the amount of colored reaction product, generated by a given amount of analyte, in proportion to the relative amounts of trapping compound and secondary substrate present in the matrix, said trapping compound being present in an amount, relative to the amount of secondary substrate in the matrix, which is effective to reduce the analyte-dependent amount of colored reaction product formed to between about 10%-70% of the colored product formed in the absence of trapping compound.

8. The test strip of claim 7, wherein said trapping agent is benzenediol which is effective to react with the oxidized 4-amino antipyrine to produce said non-colored product.

9. The test strip of claim 8, wherein said secondary substrate is N-ethyl-N-sulfohydroxy propyl-m-toluidine and said trapping compound is selected from the group consisting of 1,3-benzenediol and 1,4-benzenediol.

10. A method for assaying the concentration of an analyte in an aqueous fluid sample, where the analyte is one which can serve as a substrate for an oxidase enzyme, with the generation of H₂ O₂, comprising:

(a) adding a volume of the fluid sample to an absorptive matrix that contains (i) analyte-reaction reagents, including an analyte-specific oxidase enzyme effective to react with analyte present in such a sample to produce H₂ O₂, a peroxidase enzyme, a primary substrate which can be converted from a reduced to an oxidized form by the peroxidase enzyme in the presence of H₂ O₂, and a secondary substrate capable of reacting with the oxidized form of the primary substrate to form an analyte-dependent amount of a colored reaction product;

included in the absorptive matrix is a trapping compound which is effective to compete with the secondary substrate for reaction with the oxidized form of the primary substrate, to produce a substantially colorless product, colored reaction product generated by a given amount where the amount of trapping compound includes in the matrix is such as to reduce the analyte-dependent amount of colored reaction product formed;

(b) by said adding, reacting the analyte with the analyte-specific oxidase enzyme, whereby H₂ O₂ generated by said reacting is utilized, in the presence of peroxidase, to generate said colored and colorless reaction products, in proportion to the relative concentrations of secondary substrate and trapping compound present in the matrix; and

(c) determining the amount of colored reaction product formed in the matrix.

11. The method of claim 10, wherein said trapping compound is effective to reduce the analyte-dependent amount of said colored reaction product, as a function of analyte-concentration, to between about 10%-70% of the amount of colored reaction product formed in the absence of trapping compound.

12. The method of claim 10, for use in assaying serum cholesterol, wherein said analyte-reaction reagents further include cholesterol esterase, and said oxidase enzyme is cholesterol oxidase.

13. The method of claim 10, for use in assaying serum triglycerides, wherein said analyte-reaction reagents includes lipase, a source of ATP, and glycerol kinase, and said oxidase enzyme is glycerol-phosphate oxidase.