Compositions and methods for in vitro diagnostic tests including sulfonic acid compound
View Patent ↗The invention provides compositions, kits, and methods for performing colorimetric analysis. A substrate is reacted to generate a chromogenic reaction product, and a reaction stop reagent that is a sulfonic acid is added to stop and stabilize the reaction product. The absorbance properties of the chromogenic reaction product can be maintained over significantly longer periods of time of that of conventional reagents and methods. The sulfonic acid can be used in assays such as ELISAs in order to provide a more accurate and safer detection of analytes in a biological sample.
1. A kit for colorimetric analysis comprising:
a chromogenic substrate capable of forming a chromogenic reaction product,
wherein the chromogenic substrate is a benzidine compound of formula:
wherein X, X′, Y, Y′, R, and R′ are independently hydrogen, alkyl, alkoxy, wherein the alkyl or alkoxy group(s), if present, have four or less carbon atoms, and
a composition comprising a sulfonic acid, wherein the sulfonic acid is a compound of formula R—SO 3 H, wherein R is selected from the group consisting of methyl, ethyl, propyl, and —NH 2 , and wherein the composition is configured for addition to a solution composition comprising the chromogenic reaction product, wherein the sulfonic acid provides the solution composition with a pH of 2.0 or less.
2. The kit of claim 1 wherein;
the chromogenic substrate is tetramethylbenzidine (TMB); and
the sulfonic acid is methanesulfonic acid or sulfamic acid.
3. The kit of claim 1 further comprising a peroxidase, an oxidase, or a conjugate of a peroxidase or an oxidase.
4. The kit of claim 3 further comprising an analyte specific binding member.
5. The kit of claim 3 further comprising an analyte positive control, an analyte negative control, or mixtures thereof.
6. The kit of claim 3 further comprising an analysis plate upon which a colorimetric analysis can be performed.
7. The kit of claim 3 wherein the peroxidase and/or oxidase is selected from the group consisting of horseradish peroxidase, soybean peroxidase, glucose oxidase, galactose oxidase, xanthine oxidase, lactoperoxidase, microperoxidase, NADH peroxidase, NADPH peroxidase, fatty-acid peroxidase, and catalase.