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Kit for detecting glucose by using glucose dehydrogenase method and preparation method

A technology of glucose dehydrogenase and glucose, which is applied in the field of kits and preparations for detecting glucose by glucose dehydrogenase method, and can solve problems such as endogenous interference

Inactive Publication Date: 2013-05-08
李立和
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0015] In order to solve the problem of endogenous interference in the determination of glucose by the glucose dehydrogenase method in the prior art, the present invention provides a test kit for resisting endogenous interference and improving the accuracy of glucose determination by the glucose dehydrogenase method in clinical laboratories and Preparation

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  • Kit for detecting glucose by using glucose dehydrogenase method and preparation method
  • Kit for detecting glucose by using glucose dehydrogenase method and preparation method
  • Kit for detecting glucose by using glucose dehydrogenase method and preparation method

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Embodiment Construction

[0060] 4 bottles of glucose dehydrogenase reagent (500ml / bottle); 1 glucose standard solution (concentration: 5.55mmol / L, 2ml).

[0061] 2. Preparation of reagents:

[0062] a. The preparation method of phosphate buffer (pH7.5) 120.0mmol / L concentration phosphate buffer: weigh 96g NaCl, 2.4g KCl, 17.3g Na 2 HPO 4 and 2.88g KH 2 PO 4 , dissolved in 800ml distilled water, adjust the pH value, and finally add distilled water to make the volume to 1L.

[0063] b. Reagent preparation method: Add glucose dehydrogenase to the prepared phosphate buffer, dissolve sodium oxalate, mutarotase, NAD in sequence + , Mix well, so that the concentration of each component reaches 8.0mmol / L sodium oxalate, glucose dehydrogenase 6000U / L, mutarotase 180U / L, NAD+4.0mmol / L, 0.2% ProClin 300.

[0064] c. Preparation method of glucose standard solution: Weigh glucose (analytical grade, molecular weight: 180.16) and dissolve it in distilled water to make the concentration 5.55mmol / L. After mixing,...

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Abstract

The invention discloses a kit for detecting glucose by using a glucose dehydrogenase method, and belongs to the kit for detecting glucose containing enzymes. The kit disclosed by the invention comprises 4 bottles of glucose dehydrogenase method reagents and a glucose standard solution. The kit disclosed by the invention comprises 8.0mmol / L of sodium oxalate dissolved in the phosphate buffer solution of which the concentration is 120.0mmol / L, 6000U / L of glucose dehydrogenase, 180U / L of mutarotase, 4.0 mmol / L of NAD + (Nicotinamide Adenine Dinucleotide), and 0.2% of ProClin300 preservative. In the determination, the sodium oxalate inhibits activities of endogenous lactate dehydrogenase and alpha-hydroxybutyrate dehydrogenase to control interfere reaction, so as to increase the specificity of the reaction, and improve the accuracy of detection results. The kit disclosed by the invention is less affected by a sample / reagent volume ratio during a detecting process, and the linear range is up to 35.0mmol / L. The use method of the kit is identical with the original glucose dehydrogenase method, so that the kit does not increase the burden on an experimenter, and almost does not increase the cost of the reagent, is economical, convenient and easy and is the kit for determining glucose by using glucose dehydrogenase method with high accuracy.

Description

technical field [0001] The invention belongs to an enzyme-containing glucose detection kit, in particular to a glucose dehydrogenase detection kit and a preparation method. Background technique [0002] There are as many as 12 known determination methods for glucose. Among these methods, some methods are susceptible to high or low deviation due to the interference of reducing substances and other sugars in the reaction solution and are rarely used. At present, the most commonly used method for detecting glucose in clinical laboratories at home and abroad is the enzymatic method. Using enzymes as reagents can improve the specificity. The glucose oxidase method is easily interfered by vitamin C, uric acid, urea, bilirubin, and creatinine. The substance does not interfere with the glucose dehydrogenase method. At present, the glucose dehydrogenase method kits used in various laboratories have different manufacturers, but the composition of the kits is basically similar. The bu...

Claims

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Application Information

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IPC IPC(8): C12Q1/54C12Q1/533C12Q1/32
Inventor 李立和
Owner 李立和
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