Analytical method and element for protein assay

• US 4,786,605 A
• Filed: 06/22/1987
• Issued: 11/22/1988
• Est. Priority Date: 06/22/1987
• Status: Expired due to Term

• Current Assignee: Clinical Diagnostic Systems Inc.
• Original Assignee: Eastman Kodak Company
• Inventors: Mauck, John C., Warren, Harold C. III
• Primary Examiner(s): Marcus, Michael S.
• Assistant Examiner(s): Alfandary-Alexander, Lyle
• Application Number:
  US07/064,640
• Time in Patent Office: 519 Days
• Field of Search: 422/56, 422/57, 422/58, 436/86, 436/82, 436/88, 436/164, 436/161
• US Class Current: 436/86
• CPC Class Codes: G01N 33/526 the element being adapted for a specific analyte
• CPC Class Codes: G01N 33/6833 Copper, e.g. Folin-, Lowry-, biuret methods

Abstract

There is disclosed a method for quantitatively determining protein, comprising the steps of:

(a) providing a sample of the protein in an aqueous medium;

(b) providing an aqueous medium having a pH in excess of 12 and comprising

(i) a cupric salt and a pyridyl-azo dye; or

(ii) a preformed cupric-pyridylazo dye complex;

(c) combining the aqueous mediums of a) and b) thereby providing a color having an intensity which is inversely proportional to the amount of unreacted dye present in the combined mediums; and

(d) determining the quantity of protein present in the sample colorimetrically.

The method can be used with a multilayer dry analytical element.

Claims

1. A method for quantitatively determining protein, comprising the steps of:

(a) providing a sample of the protein in an aqueous medium;

(b) providing an aqueous medium having a pH in excess of 12 and comprising

(i) a cupric salt and a pyridyl-azo dye;

or

(ii) a preformed cupric-pyridyl-azo dye complex;

(c) combining the aqueous mediums of (a) and (b) thereby forming a color having an intensity which is inversely proportional to the amount of unreacted dye present in the combined mediums; and

(d) determining the quantity of protein present in the sample colorimetrically.

2. The method of claim 1 wherein the dye has the structure ##STR3## wherein R represents --OH, NH₂ or dialkylamino;

R¹ represents H, OH, NH₂ or dialkylamino;

R² represents H, NH₂, or OH;

R³ represents H or C₆ H₅ NHSO₂, CH₃ SO₂, Cl, Br, or CN;

R⁴ represents H, (CH₃)₂ NSO₂ or NO₂ or R⁴, together with R⁵ and the carbon atoms to which they are attached form a fused phenyl group.

3. The method of claim 2 wherein R represents OH, NH₂ or COOH.

4. The method of claim 1 or 2 wherein the dye is ##STR4## and the cupric salt is Cu⁺² (ethylacetoacetate)₂.

5. The method of claim 1 wherein the colorimetric measurement is taken at 670 nanometers.

6. An analytical element for determination of protein in an aqueous medium comprising an absorbent material which contains

(i) a cupric salt and a pyridyl-azo dye or a preformed cupric-pyridyl-azo dye complex and

(ii) a base composition capable of establishing a pH in excess of 12 when the absorbent material is contacted with an aqueous medium.

8. The element of claim 6 or 7 wherein the pyridyl-azo dye has the structure ##STR5## wherein R represents an electron donor;

R¹ represents H, OH, NH₂ or dialkylamino;

R² represents H, NH₂, or OH;

R³ represents H or C₆ H₅ NHSO₂, CH₃ SO₂, Cl, Br, or CN;

R⁴ represents H, (CH₃)₂ NSO₂ or NO₂, dimethylamino or R⁴, together with R⁵ and the carbon atoms to which they are attached form a fused phenyl group.

9. The element of claim 6 or 7 wherein the cupric salt is Cu⁺² (ethylacetoacetate)₂ and the dye is ##STR6##

12. The element of claim 6 or 7 wherein the base composition is a mixture of lithium hydroxide and poly(acrylamide-co-N-vinyl-2-pyrolidone) in weight ratio of 50:

1.

13. The element of claim 6 or 7 wherein the copper salt is Cu⁺² (ethylacetoacetate)₂ ;

the dye has the structure ##STR7## and the base composition comprises lithium hydroxide, and poly(acrylamide-co-N-vinyl-2-pyrolidone) weight ratio 50;

1.

14. The element of claim 6 or 7 comprising 0.02 to 0.3 g/m² of the copper salt and 0.02 to 0.3 g/m² of the pyridyl-azo dye.

7. A multilayer analytical element for determination of protein in an aqueous medium, comprising

(i) a support bearing,

(ii) a spreading layer,

(iii) one or two reagent layers in fluid contact with the spreading layer;

and

(iv) a cupric salt, a pyridyl-azo dye or a preformed cupric-pyridyl-azo dye complex and a base composition capable of establishing a pH in excess of 12;

wherein

the salt and the dye are in the same or different layers.

10. The element of claim 7 wherein the cupric salt is in the spreading layer and the pyridyl-azo dye is in the reagent layer.

11. The element of claim 7 wherein the dye and the cupric salt or a preformed cupric-pyridyl-azo dye complex are in the reagent layer.

15. A method for the quantitative analysis of proteins in an aqueous liquid sample which comprises

(a) providing an analytical element for the determination of protein in an aqueous medium comprising an absorbent material which contains

(i) a support bearing,

(ii) a spreading layer,

(iii) a reagent layer in fluid contact with the spreading layer, and comprising a cupric salt and a pyridyl-azo dye or a preformedd cupric-pyridyl-azo dye complex;

and

(b) applying a portion of the sample to the spreading layer of the analytical element,

(c) colorimetrically determining, after a predetermined time, the quantity of protein in the sample wherein the color intensity is inversely proportional to the amount of unreacted dye.