USPatent applicationPatented

Concentated liquid single component TMB substrate for detection assay of horseradish peroxidase

Granted 25 Jul 2017 · no office action yet

Assignee: Hao Zhang

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Inventors: Hao Zhang · Examiner: Shafiqul Haq · AU 1678 · TC 1600

Application· this page
15/409,274
filed 18 Jan 2017
Publication
Not published
not published
Patent
US 9,714,939
granted 25 Jul 2017

Life of the application

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Abstract

Through special formulations, stable twenty-fold concentrate of single component TMB substrate is produced to minimize the volume and reduce the transportation cost. Reconstitution of the concentrate upon delivery to the distal site can be made with deionized water to yield single component TMB substrate solution for routine immunodiagnostic applications.

Description

5 parts
›This application claims the benefit of U.S. Provisional…

This application claims the benefit of U.S. Provisional Application No. 62/307,549 filed on Mar. 13, 2016, entitled “Hao Zhang”

›BACKGROUND OF INVENTION

The present invention relates to the concentrated forms of TMB substrate in the field of immunoassays by using horseradish peroxidase (HRP) for the enzyme labeling of detection antibodies. Preferably, single component TMB substrate is used for the signal detection during various forms of immunoassays. The stability and concentrated forms of such TMB substrate become desirable during the large scale practical applications in immunodiagnostics to facilitate the transportation to distal or remote sites.

›SUMMARY OF INVENTION

The present invention relates to the formulations of single component TMB substrate in concentrated form to facilitate the distant transport of liquid substrate component in its concentrated form. The key production protocols required the formulations of TMB substrate in high concentration (20 fold concentrate or higher) with good solubility and stability. To achieve this goal, a protocol is disclosed have to ensure TMB solubility as stability under such concentration at room temperature for 24-36 months.

In the process of the present invention, the addition of polyhydroxy alcohol such as glycerol, and low molecular weight PEG would enhance the solubility of TMB in high concentrations. EDTA at specific PH provides protection of TMB oxidation by heavy transition metals. Notably, encasing of TMB with β-cyclodextrin in essential for the stability of TMB during the long term storage. This encasing process of TMB has been widely disclosed in several previous inventions. Thus in brief summary, the current invention involves the inclusion of special polyhydroxyl organic solvents to enhance the solubility of the encasing TMB in the final concentration forms for long term stability during storage and transport at room temperature.

›DETAILS DESCRIPTION OF THE INVENTION

Abbreviated names of organic compounds.

DMSO—dimethyl sulfoxide TMB—3,3′,5,5′ tetramethylbenzidine BCD—β-cyclodextrin PEG—polyethyle glycol of defined molecular weight (<2000) EDTA—ethylediamine tetra-acetic acid H 2 O 2 — hydrogen peroxide HCl—Hydrochloric acid

As noted, TMB has been widely accepted as an excellent peroxidase substrate. The mechanism of action in using TMB substrate during enzyme immunoassay with peroxidase has been well established for decades. Methods of preventing spontaneous oxidation of TMB and subsequent precipitation have been elucidated previously. This will lead to the storage shell life of TMB reagent to as long as 36 months or longer. Therefore, polyhydroxy alcohol has been shown to increase solubility of TMB or encased TMB in mixture of organic solvents and H 2 O.

›EXAMPLE 1

The Production of A twenty fold concentrated TMB Solution for ELISA Methods is described as follows: The reagents that are required to formulate twenty fold plus TMB concentrate are listed in the preferred weigh or final volume per 100 ml by the following table:

Reagent Preparations Prior to Final Production of concentrate of one step TMB.

1. The resistance of deionized water should be greater than 18 megohm. 2. Preparation of BCD solution. 10 ml deionized water, 2 g, stirred until 2 g BCD is dissolved. 3. Additions of other chemicals are given as listed in the Table except for TMB and DMSO (sec 4.) and H 2 O 2 . 4. Prepare 1.3 g TMB in 40 ml DMSO with constant stirring 5. The final solution should consist of all the chemical reagents listed on the table with PH of the final solution adjusted to pH3.6+ or −0.02 with N HCl. 6. Deionized water was added until the final solution one step TMB concentrate to reach to 100 ml with 5-10 hours of constant stirring at 40-50° C. until all solid materials are fully dissolved.

›Tables in the description — 1
Nameml (g)/100 ml
a. Glycerol10ml
b. PEG200010g
c. DMSO10ml
d. TMB1.3g
e. BCD2g
f. EDTA0.24g
g. Citric Acid2g
h. H 2 O 20.22%
i. Isopropanol5ml
j. Fumaric Acid1g
k. Distill H 2 O70ml
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Classifications

6 codes
IPC · International Patent Classification
Section A — Human necessities
  • A61K47/10
  • A61K47/40
  • A61K47/08
Section C — Chemistry; metallurgy
  • C12Q1/28
Section G — Physics
  • G01N33/58
  • G01N33/535

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Pendency
0.5 y
188 days filing → grant
Office actions
0
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Examiner
Shafiqul Haq
art unit 1678 · TC 1600
Citations: 2 back · 3 forward

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