Determination of blood ammonia content and blood ammonia diagnostic reagent kit

A diagnostic kit and blood ammonia technology, applied in the field of medical testing and determination, can solve the problems of high recovery rate, no detection method of blood ammonia, influence of accuracy and precision, etc.

Inactive Publication Date: 2006-05-31
SUZHOU ANJ BIOTECHNOLOGY CO LTD
View PDF1 Cites 24 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

These methods require alkalization, which is affected by the formation of endogenous ammonia, which affects its accuracy and precision, and is rarely used at present; the ion exchange method is more accurate than the diffusion method, and the CV is 8%-13%; Selective electrode method is to use NH 3 Diffusion to the surface of the electrode, causing the pH of the electrode to

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0082] Embodiment one (single dose)

[0083] The blood ammonia diagnostic kit of the present embodiment comprises:

[0084] Buffer 80mmol / l

[0085] 2-ketoglutarate 5mmol / l

[0086] Reduced coenzyme 0.2mmo / l

[0087] Adenosine triphosphate 2mmol / l

[0088] Phosphoenolpyruvate 2mmol / l

[0089] Glutamate dehydrogenase 5000U / l

[0090] Glutamate kinase 5000U / l

[0091] Pyruvate Kinase 1000U / l

[0092] Lactate dehydrogenase 5000U / l

[0093] Stabilizer 50% (total volume)

[0094] Set on the automatic biochemical analyzer: temperature 37°C, reaction time 10 minutes, test main wavelength 340nm, test sub-wavelength above 405nm, the volume ratio of the measured blood ammonia sample to reagent is 1 / 25, and the reaction direction is negative reaction .

[0095] After the sample and reagents are added and allowed to mix, the following reactions occur:

[0096] Ammonium ion + 2-ketoglutarate + reduced coenzyme glutamate dehydrogenase

[0097] Glutam...

Embodiment 2

[0105] Embodiment two (two doses)

[0106] The blood ammonia diagnostic reagent of the present embodiment has:

[0107] Reagent I

[0108] Buffer 100mmol / l

[0109] 2-ketoglutarate 12mmol / l

[0110] Reduced coenzyme 0.25mmo / l

[0111] Adenosine triphosphate 5mmol / l

[0112] Phosphoenolpyruvate 5mmol / l

[0113] Glutamate kinase 12000U / l

[0114] Pyruvate kinase 6000U / l

[0115] Lactate dehydrogenase 12000U / l

[0116] Stabilizer 50% (total volume)

[0117] Reagent II

[0118] Buffer 100mmol / l

[0119] Glutamate dehydrogenase 12000U / l

[0120] Stabilizer 50% (total volume)

[0121]When measuring the blood ammonia content, the temperature is controlled at 30°C, the reaction time is 15 minutes, the main wavelength of the test is 340nm, the secondary wavelength of the test is above 405nm, the volume ratio of the blood ammonia sample to the reagent is 1 / 25, and the reaction direction is negative reaction.

[0122] The specific measurement steps are:

[0123] Ammonium io...

Embodiment 3

[0132] Embodiment three (three doses)

[0133] The blood ammonia diagnostic reagent of the present embodiment is three doses, has:

[0134] Reagent I

[0135] Buffer 120mmol / l

[0136] 2-ketoglutarate 20mmol / l

[0137] Reduced coenzyme 0.3mmo / l

[0138] Adenosine triphosphate 8mmol / l

[0139] Phosphoenolpyruvate 8mmol / l

[0140] Stabilizer 20mmol / l

[0141] Reagent II

[0142] Buffer 120mmol / l

[0143] Glutamate kinase 20000U / l

[0144] Pyruvate Kinase 10000U / l

[0145] Lactate dehydrogenase 20000U / l

[0146] Stabilizer 50% (total volume)

[0147] Reagent III

[0148] Buffer 120mmol / l

[0149] Glutamate dehydrogenase 20000U / l

[0150] Stabilizer 50% (total volume)

[0151] Set on the automatic biochemical analyzer: temperature 25°C, reaction time 20 minutes, test main wavelength 340nm, test sub-wavelength above 405nm, the volume ratio of the measured blood ammonia sample to reagent is 1 / 25, and the reaction direction is negative reaction .

[0152] The specifi...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention is about a method of measuring the content of blood ammonia, and it also concerns the reagent box of blood ammonia diagnosis. This invention belongs to the field of medical testing and measuring technology. The reagent box is consisted of buffer solution, 2ú¡ketoglutarate, reduced coenzyme, adenosine triphosphate, phosphoenolpyruvate, glutamate dehydrogenase, glutamate kinase, pyruvate kinase, lactate dehydrogenase and stabilizer. Firstly, we cause an enzyme-coupled reaction through mixing the sample and the reagent according to a certain proportion of volume; secondly, put the final reactant under the biochemical analyzer and test the absorbance variational situation (speed) of dominant wavelength; then we can get the content of blood ammonia. By using this invention, we can get the necessary measuring result with high sensitiveness and fine precision through biochemical analyzer, and the result would not be contaminated by material of internal and exogenous sources. Thus, this method can be conveniently promoted and applied.

Description

technical field [0001] The invention relates to a method for measuring blood ammonia content, and at the same time, the invention also relates to a blood ammonia diagnosis kit, which belongs to the technical field of medical examination and measurement. Background technique [0002] Ammonia determination methods include micro-diffusion method, ion exchange method, enzymatic method and ammonia electrode method. The most widely used methods are enzymatic method and blood ammonia analyzer analysis method based on ion selective electrode. [0003] The diffusion method is that after the sample is alkalized, NH is released 3 , Titrate the released ammonia with acid, or use the Nessler reaction to form brown-yellow mercuric ammonium iodide for colorimetry. These methods require alkalization, which is affected by the formation of endogenous ammonia, which affects its accuracy and precision, and is rarely used at present; the ion exchange method is more accurate than the diffusion ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C12Q1/48
Inventor 王尔中
Owner SUZHOU ANJ BIOTECHNOLOGY CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products