Stabilization of H
View Patent ↗The invention relates to stannous halide stabilized and/or enhanced alkaline solutions to be used in combination with colorimetric, luminescent and fluorescent assays. The buffered solutions stabilize hydrogen peroxide at a pH greater than 7.0 and preferably greater than 9.0. By stabilizing and/or enhancing hydrogen peroxide in the buffer system, the compositions used in such assays may have a higher shelf-life and provide enhanced detection of the subject analyte.
1. A composition for use in a fluorescent, luminescent or colorimetric assay comprising a heme containing protein, a peroxide, a peroxide stabilizing and/or enhancing amount of a stannous halide and an alkaline buffer, and wherein said composition has a pH of about 8.0 or greater.
2. The composition of claim 1 , wherein the peroxide stabilizing and/or enhancing amount of the stannous halide is in the amount of about 0.005% to about 5.0%.
3. The composition of claim 1 , wherein the peroxide stabilizing and/or enhancing amount of stannous halide is in the amount of about 1 mg/L to about 50 mg/L.
4. The composition of claim 1 , wherein the stannous halide is stannous fluoride or stannous chloride.
5. The composition of claim 1 , wherein the heme containing protein is a catalase, a peroxidase, a hemoglobin, a myoglobin, a ferritin, or a cytochrome oxidase.
6. The composition of claim 5 , wherein said peroxidase is horseradish peroxidase.
7. The composition of claim 1 , wherein the alkali buffer is a phosphate buffer, an aminomethylpropanediol buffer, a glycine-sodium hydroxide buffer, a barbitol buffer, a tricine buffer, a Bis-Tris buffer, a Tris buffer, an imidazole buffer, a sodium tetraborate decarbohydrate buffer, a sodium carbonate buffer, or a CHAPS buffer.
8. The composition of claim 1 , wherein said peroxide is hydrogen peroxide.
9. The composition of claim 1 , wherein said composition further comprises a substrate.
10. The composition of claim 9 , wherein said substrate is a chromagen, a chemifluorescent compound, a chemiluminescent compound, or a bioluminescent compound.
11. The composition of claim 10 , wherein said chromagen is 4CN, 5AS, ABTS, AEC, DAB, Hanker-Yates, o-dianisidine, OPD, PPD or TMB.
12. The composition of claim 10 , wherein said chemiluminescent compound is luminol, a diacyl hydrazide, isoluminol, or a polyphenol.
13. The composition of claim 12 , wherein said polyphenol is purpurogallin, pyrogallol, gallic acid, or umbelliferone.
14. A kit for conducting an assay for detecting the presence or concentration of a heme containing protein in a sample which comprises in one or more containers:
(A) a substrate which is rendered detectable by said heme containing protein;
(B) a peroxide;
(C) an alkaline buffer; and
(D) a peroxide stabilizing and/or enhancing amount of a stannous halide;
and wherein the substrate, the peroxide, the alkaline buffer, and the stannous halide when admixed have a pH of about 8.0 or greater.
15. The kit of claim 14 , wherein said heme containing protein is a peroxidase, a hemoglobin, a myoglobin, a catalase, a cytochrome oxidase, or a ferritin.
16. The kit of claim 15 , wherein said peroxidase is horseradish peroxidase.
17. The kit of claim 14 , wherein said alkaline buffer is a phosphate buffer, an aminomethylpropanediol (AMPD) buffer, a glycine-sodium hydroxide buffer, a barbitol buffer, a Bis-Tris buffer, a sodium carbonate buffer, a Tris buffer, a tricine buffer, an imidazole buffer, a sodium tetraborate decarbohydrate buffer, or a CHAPS buffer.
18. The kit of claim 14 , wherein said peroxide is H 2 O 2 .
19. The kit of claim 14 , wherein said substrate comprises a colorimetric compound, a chemiluminescent compound, or a chemifluorescent compound.
20. The kit of claim 19 , wherein said substrate is a colorimetric compound selected from the group consisting of 3-amino-9-ethylcarbazole (AEC), 3,3′,4,4′-diaminobenzidene (DAB), 3,3′,5,5′-tetramethylbenzidine (TMB), 2,2′-azino-di[3-ethylbenzthiazolin] sulfonate) (ABTS), 4-chloro-1-naphthol (4CN), 5-aminosalicyclic acid (5AS), o-phenylenediamine (OPD), Hanker-Yates, p-phenylenediamine (PPD), and o-dianisidine.
21. The kit of claim 19 , wherein said substrate is a chemiluminescent compound selected from the group consisting of luminol, isoluminol, a polyphenol, and a diacyl hydrazide.
22. The kit of claim 21 , wherein said chemiluminescent compound is luminol or isoluminol and said kit further comprises a peroxidase activity enhancer selected from the group consisting of: N,N-dimethylindo-(aniline), 2,6-dichlorophenolindo-o-cresol, phenolindophenol, N-methylphenothiazine, and mixtures thereof.
23. The kit of claim 21 , wherein said chemiluminescent compound is a polyphenol and is pyrogallol, purpurogallin, gallic acid, or umbelliferone.
24. The kit of claim 19 , wherein said substrate is a chemifluorescent compound selected from the group consisting of hydroxyphenylacetic acid (HPA) 3-p-hydroxyphenylproprionic acid (HPPA), and 10-acetyl-3,7-dihydroxyphenoxazine.
25. The kit of claim 14 , wherein components are admixed at a pH of about 8.0 to about 10.0.
26. The kit of claim 14 , wherein components are admixed at a pH of about 9.5.
27. The kit of claim 14 , which further comprises a compound which binds specifically to said heme containing protein.
28. The kit of claim 27 , which further comprises a compound which binds specifically to said compound which binds specifically to said heme containing protein.
29. The kit of claim 27 , wherein said compound which binds to said heme containing protein is a nucleic acid or a polypeptide.
30. The kit of claim 28 , wherein said compound which binds to said compound which binds to said heme containing protein is a nucleic acid or a polypeptide.