Multifunctional dry plate test board and preparation method and application thereof
A detection board, a multifunctional technology, applied in the preparation of test samples, biochemical equipment and methods, biological testing, etc., can solve the problems of low detection efficiency, not very wide application, hindering the development and comprehensive popularization of detection technology, etc. Achieve the effects of high degree of automation, fast detection speed, scientific design and development and technical route
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[0022] Example 1 ALT dry film detection board
[0023] The ALT dry slice detection plate is based on the pyruvate oxidase method to quantitatively detect alanine aminotransferase in human blood samples. First, ALT catalyzes the conversion of alanine and α-ketoglutarate to pyruvate and glutamic acid. Pyruvate and phosphate, O 2 When oxidized under the catalysis of pyruvate oxidase, acetyl phosphate and hydrogen peroxide are generated. The generated hydrogen peroxide has strong oxidizing properties and can oxidize the reducing color developer to produce color changes. The reaction formula is as follows:
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[0027] Each test plate contains the following biochemical reaction reagents:
[0028] L-alanine 168~252μg
[0029] α-ketoglutarate 15.7~25.6μg
[0030] TPP 10.9~17.4μg
[0031] MgCl 2 1.7~2.4μg
[0032] Pyruvate oxidase 1.9~2.8U
[0033] Peroxidase 18.0~26.3U
[0034] Chromogenic agent 24.8~35.6μg
[0035] Preparation of ALT dry sli...
Example Embodiment
[0043] Example 2 (Detection board for blood lipids and blood sugar dry tablets)
[0044] The blood lipid and blood sugar dry film detection board is based on the cholesterol oxidase method, the glycerol phosphate oxidase method, and the glucose oxidase method to quantitatively detect the total cholesterol, high-density lipoprotein, triglycerides and glucose in human blood samples. The reaction equations are as follows:
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[0054] Each test plate contains the following biochemical reaction reagents:
[0055] Cholesterol esterase 0.1~0.9U
[0056] Cholesterol oxidase 0.01~0.07U
[0057] Glycerin kinase 0.2~0.7U
[0058] Phosphoglycerol oxidase 0.1~0.9U
[0059] Horseradish peroxidase 0.1~0.5U
[0060] MgCl 2 1.7~2.4μg
[0061] Glucose oxidase 0.2~1U
[0062] ATP 18~26μg
[0063] Chromogenic agent 50~120μg
[0064] Preparation of blood lipids and blood sugar dry tablets
...
Example Embodiment
[0071] Example 3 Renal function (creatinine, urea nitrogen, blood potassium, carbon dioxide content) detection board
[0072] The detection principle of creatinine is based on the fact that creatinine produces creatine under the action of creatinase, creatine produces creatine under the action of creatinase, and finally creatine produces hydrogen peroxide under the action of creatine oxidase, thereby oxidizing the color reagent Color rendering.
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[0077] The detection principle of urea nitrogen is based on the formation of ammonia under the action of urease, and the colour of ammonia under the action of sodium hypochlorite and sodium salicylate.
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[0080] The detection principle of serum potassium is based on the ionophore (2,3-naphtho-15-crown-5) in the reaction system that once specifically binds to potassium ions, the reporter substrate (7-decyl-MEDPIN) will lose protons and change Its color.
[0081] The detection...
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