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Enzymatic chemiluminescence based detection kit for UA (uric acid) determination

A detection kit and luminescence technology, applied in the biological field, can solve the problems of low specificity, interference and poor stability of peroxidase, and achieve the effects of enhancing anti-interference ability, reducing interference and high sensitivity

Active Publication Date: 2018-06-01
GUANGZHOU JINDE BIOTECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, this method uses luminol, isoluminol and their derivatives as luminescent substrates, which generally need to add catalysts such as peroxidase. The stability of these reagent components is poor, and the specificity of peroxidase The sensitivity is not high, because hydrogen peroxide is the main intermediate product in this reaction, it is easy to be interfered in the determination process
[0005] Secondly, what cannot be ignored in the process of detecting uric acid at present is the interference caused by endogenous substances in the sample such as hemoglobin, bilirubin and exogenous substances derived from clinical drug applications, such as ascorbic acid, which leads to the detection of uric acid. There is a certain difference between the result and the real value

Method used

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  • Enzymatic chemiluminescence based detection kit for UA (uric acid) determination
  • Enzymatic chemiluminescence based detection kit for UA (uric acid) determination
  • Enzymatic chemiluminescence based detection kit for UA (uric acid) determination

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Embodiment 1, the preparation of Tween 80 primary degradant

[0038] Add Tween 80 solution into a 100ml shake flask, inoculate 1~3wt% Trichoderma viride with a concentration of 1000cfu / mL, set the temperature at 35°C, rotate at 120r / min, cultivate for 12h, centrifuge, and take the supernatant; Microfiltration was performed on clear water, cation exchange and sterilization were performed on 732 type cation exchange resin, and the primary degradation product of Tween 80 was obtained.

Embodiment 2

[0039] Example 2, a detection kit for the determination of uric acid by enzymatic chemiluminescence

[0040] Reagent R1:

[0041]

[0042] Reagent R2:

[0043]

[0044] Reagent R3:

[0045] Lumigen HyPerBlu.

Embodiment 3

[0046] Example 3, a detection kit for the determination of uric acid by enzymatic chemiluminescence

[0047] The difference between Example 3 and Example 2 is that the anti-interference agent I in the reagent R1 is ascorbate oxidase and potassium ferrocyanide, the concentration of the primary degradation product of Tween 80 is 0.03w / v%, and the remaining parameters and operations are as implemented Example 2 shows.

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Abstract

The invention belongs to the technical field of biology and particularly relates to an enzymatic chemiluminescence based detection kit for UA (uric acid) determination. UA is oxidized into allantoin and hydrogen peroxide under catalysis of uricase, hydrogen peroxide is subjected to direct reaction with a luminescence substrate, and a persistent high-intensity chemical signal is formed without peroxidase. Compared with the traditional enzymatic colorimetry and chemiluminescence, hydrogen peroxide is subjected to direct reaction with the substrate for luminescence without need of adding catalasefor catalysis, and the method can be applied to full-automatic luminescence instruments and can meet clinical automatic batch detection.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to a detection kit for measuring uric acid by an enzyme chemiluminescence method. Background technique [0002] The molecular formula of uric acid (2,4,6-trihydroxypurine, referred to as UA) is C 5 h 4 N 4 o 3 , its molecular weight MW=168.11. It is a white crystalline substance that is insoluble in water, acid, ether and ethanol. It is weakly alkaline and can form a salt with strong acid. Uric acid exists in the form of salt in the living body, so it has a high solubility. Uric acid is the end product of purine metabolism in the human body. Most of it is excreted with urine, and a small part is excreted through feces and sweat. Normal value of plasma uric acid: male: 149-416 μmol / L, female: 89-357 μmol / L. When the purine metabolism in the human body is disturbed, the concentration of uric acid in the plasma is too high, which is called hyperuricemia (HUA). The solub...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N33/53
CPCG01N33/5308G01N2333/902
Inventor 李民友林伟荣张玲蔺涛
Owner GUANGZHOU JINDE BIOTECH
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