Ascorbate interference-resistant composition, device and method for the determination of peroxidatively active substances

• US 4,587,220 A
• Filed: 02/02/1984
• Issued: 05/06/1986
• Est. Priority Date: 03/28/1983
• Status: Expired due to Term

• Current Assignee: Miles Laboratories, Inc. (Bayer AG)
• Original Assignee: Miles Laboratories, Inc. (Bayer AG)
• Inventors: Mayambala-Mwanika, Christine, White-Stevens, Rodric H.
• Primary Examiner(s): Turk, Arnold
• Application Number:
  US06/575,725
• Time in Patent Office: 824 Days
• Field of Search: 422/56, 422/57, 436/66, 436/135, 436/904, 436/175, 435/14, 435/28, 435/805, 427/2
• US Class Current: 436/66
• CPC Class Codes: C12Q 1/28 involving peroxidase
• CPC Class Codes: Y10S 436/904 Oxidation - reduction indicators
• CPC Class Codes: Y10T 436/25125 Digestion or removing interfering materials

Abstract

A composition, test means (and device) and method for determining peroxidatively active substances in a test sample are disclosed. The composition, test means (and device) and method are rendered resistant to the adverse affects of ascorbate which may be present in the sample by the inclusion in the composition of a metal chelate which is polycarboxyalkylamine derivative having the formula: ##STR1## where: (a) R₁ is hydrogen or straight or branched chain alkyl alcohol or alkyl carboxylic acid radicals having from 2 to 3 carbon atoms; R₂, R₃, R_x and R_y, same or different, are straight or branched chain alkyl alcohol or alkyl carboxylic acid radicals having from 2 to 3 carbon atoms; where at least two of R₁, R₂, R₃, R_x or R_y are alkyl carboxylic acid radicals so defined;

(b) R_p and R_q, same or different, are straight or branched chain alkylene radicals having from 1 to 3 carbon atoms or divalent 1,2-cycloaliphatic radicals having from 6 to 9 carbon atoms;

(c) n is an integer having a value of from 0 to 1; m is an integer having a value of from 0 to 2; where if m is greater than 0, repeated R_p and repeated R_q radicals may be the same or different; and

(d) M is Fe⁺³.

The composition also comprises an organic hydroperoxide and an indicator capable of providing a detectable response in the presence of peroxide and the peroxidatively active substance. The test means comprises a carrier matrix incorporated with the composition, and the method comprises immersing the test means (or device) in the test sample and observing a color or other detectable response.

Claims

1. In a composition for detecting the presence of a peroxidatively active substance in a test sample, the composition comprising an organic hydroperoxide and an indicator capable of providing a detectable response in the presence of the peroxidatively active substance and peroxide,

the improvement wherein the composition additionally comprises a metal chelate of a polycarboxyalkylamine derivative having a general formula:

##STR4## where;

(a) R₁ is hydrogen or straight or branched chain alkyl alcohol or alkyl carboxylic acid radicals having from 2 to 3 carbon atoms;

R₂, R₃, R_x and R_y, same or different, are straight or branched chain alkyl alcohol or alkyl carboxylic acid radicals having from 2 to 3 carbon atoms;

where at least two of R₁, R₂, R₃, R_x or R_y are alkyl carboxylic acid radicals so defined;

(b) R_p and R_q, same or different, are straight or branched chain alkylene radicals having from 1 to 3 carbon atoms or divalent 1,2-cycloaliphatic radicals having from 6 to 9 carbon atoms;

(c) n is an integer having a value of from 0 to 1;

m is an integer having a value of from 0 to 2;

where if m is greater than 0, repeated R_p and repeated R_q radicals may be the same or different; and

(d) M is Fe⁺³.

2. The composition of claim 1 in which

(a) m is 0;

and

(b) R_p is an ethylene radical.

3. The composition of claim 1 in which at least two of R₁, R₂, R₃, R_x and R_y are the alkyl carboxylic acid radical, --CH₂ COOH.

4. The composition of claim 1 in which the indicator is benzidine;

o-tolidine;

a 3,3'"'"',5,5'"'"'-tetra(lower alkyl)benzidine;

2,7-diaminofluorene;

or mixtures thereof.

5. The composition of claim 1 in which the metal chelate is selected from the group consisting of ferric chelates of N-(2-hydroxyethyl)ethylenediaminetriacetic acid, ethylenediaminetetraacetic acid, cyclohexylenediaminetetraacetic acid, nitrilotriacetic acid, iminodiacetic acid, α

-ethylenediaminediaceticdipropionic acid, β

-ethylenediaminediaceticdipropionic acid, hydroxylethylaminodiacetic acid and mixtures thereof.

6. The composition of claim 1 in which the metal chelate is a ferric chelate of N-(2-hydroxyethyl)-ethylenediaminetriacetic acid.

7. The composition of claim 1 in which the metal chelate is a ferric chelate of ethylenediaminetetraacetic acid.

8. The composition of claim 1 in which the organic hydroperoxide is selected from the group consisting of cumene hydroperoxide;

t-butyl hydroperoxide, diisopropylbenzene hydroperoxide, 2,5-dimethylhexane-2,5-dihydroperoxide;

paramenthane hydroperoxide; and

mixtures thereof.

9. The composition of claim 1 in which organic hydroperoxide is cumene hydroperoxide and the indicator is 3,3'"'"',5,5'"'"'-tetramethylbenzidine.

10. The composition of claim 1 in which the indicator is 3,3'"'"',5,5'"'"'-tetramethylbenzidine, the metal chelate is a ferric chelate of N-(2-hydroxyethyl)-ethylenediaminetriacetic acid and the organic hydroperoxide is cumene hydroperoxide.

11. A test means for determining the presence of a peroxidatively active substance in a test sample, comprising a carrier matrix incorporated with the composition of claim 1.

12. A test means for determining the presence of a peroxidatively active substance in a test sample, comprising a carrier matrix incorporated with the composition of any of claims 2 to 10.

23. A method for determining the presence of a peroxidatively active substance in a test sample, comprising the steps of contacting the sample with the test means of claim 11 and observing a detectable response.

13. A method for preparing a test means for determining the presence of a peroxidatively active substance in a test sample, wherein the test means is resistant to interfering affects of ascorbate which may be present in the sample, which method comprises the steps of:

(a) preparing a first reagent solution including an organic hydroperoxide, and a metal chelate of an polycarboxyalkylamine derivative having the general formula;

##STR5## where;

(i) R₁ is hydrogen or straight or branched chain alkyl alcohol or alkyl carboxylic acid radicals having from 2 to 3 carbon atoms;

R₂, R₃, R_x and R_y, same or different, are straight or branched chain alkyl alcohol or alkyl carboxylic acid radicals having from 2 to 3 carbon atoms;

where at least two of R₁, R₂, R₃, R_x or R_y are alkyl carboxylic acid radicals so defined;

(ii) R_p and R_q, same of different, are straight or branched chain alkylene radicals having from 1 to 3 carbon atoms or divalent 1,2-cycloaliphatic radicals having from 6 to 9 carbon atoms;

(iii) n is an integer having a value of from 0 to 1;

m is an integer having a value of from 0 to 2;

where if m is greater than 0, repeated R_p and repeated R_q radicals may be the same or different; and

(iv) M is Fe⁺³ ;

(b) incorporating the first reagent solution with a carrier matrix by wetting the matrix with the first solution;

(c) drying the wetted matrix to leave a residue of the metal chelate and the hydroperoxide;

(d) preparing a second reagent solution including an indicator and a solvent, the indicator being capable of providing a detectable response in the presence of a peroxide and the peroxidatively active substance;

(e) incorporating the second reagent solution with the dried carrier matrix by wetting the matrix with the second reagent solution; and

(f) drying the matrix to leave a combined residue including the metal chelate, the hydroperoxide and the indicator.

14. The method of claim 13 in which

(a) m is 0;

and

(b) R_p is an ethylene radical.

15. The method of claim 13 in which at least two of R₁, R₂, R₃, R_x and R_y are the alkyl carboxylic acid radical, --CH₂ COOH.

16. The method of claim 13 in which the indicator is benzidine;

o-tolidine;

a 3,3'"'"',5,5'"'"'-tetra(lower alkyl)benzidine;

2,7-diaminofluorene;

or mixtures thereof.

17. The method of claim 13 in which the metal chelate is selected from the group consisting of ferric chelates of N-(2-hydroxyethyl)ethylenediaminetriacetic acid, ethylenediaminetetraacetic acid, cyclohextlenediaminetetraacetic acid, nitrilotriacetic acid, iminodiacetic acid, α

-ethylenediaminediaceticdipropionic acid, β

-ethylenediaminediaceticdipropionic acid, hydroxylethylaminodiacetic acid and mixtures thereof.

18. The method of claim 13 in which the metal chelate is a ferric chelate of N-(2-hydroxyethyl)-ethylenediaminetriacetic acid.

19. The method of claim 13 in which the metal chelate is a ferric chelate of ethylenediaminetetraacetic acid.

20. The method of claim 13 in which the organic hydroperoxide is selected from the group consisting of cumene hydroperoxide;

t-butyl hydroperoxide, diisopropylbenzene hydroperoxide, 2,5-dimethylhexane-2,5-dihydroperoxide;

paramenthane hydroperoxide; and

mixtures thereof.

21. The method of claim 13 in which organic hydroperoxide is cumene hydroperoxide and the indicator is 3,3'"'"',5,5'"'"'-tetramethylbenzidine.

22. The method of claim 13 in which the indicator is 3,3'"'"',5,5'"'"'-tetramethylbenzidine, the metal chelate is a ferric chelate of N-(2-hydroxyethyl)-ethylenediaminetriacetic acid and the hydroperoxide is cumene hydroperoxide.