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Determination of inorganic phosphorus and its diagnostic reagent kit

A diagnostic kit and inorganic phosphorus technology are applied in the field of medical testing and determination, which can solve problems such as influence on use and promotion, differences in the accuracy of sensitivity test results, etc.

Inactive Publication Date: 2006-05-31
SUZHOU ANJ BIOTECHNOLOGY CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, with different reagents and testing routes, the sensitivity of detection and the accuracy of detection results will be very different, which directly affects the use and promotion of this method.

Method used

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  • Determination of inorganic phosphorus and its diagnostic reagent kit
  • Determination of inorganic phosphorus and its diagnostic reagent kit
  • Determination of inorganic phosphorus and its diagnostic reagent kit

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0070] Embodiment one (single agent)

[0071] Prepare the diagnostic kit for inorganic phosphorus in serum according to the following components and dosage:

[0072] Glycine buffer 80mmol / l,

[0073] Inosine 0.2mmol / l,

[0074] Nucleoside phosphatase 5000U / l,

[0075] Xanthine oxidase 5000U / l,

[0076] Urease 5000U / l,

[0077] Peroxidase 5000U / l,

[0078] 4-Aminoantiarsenic 2mmol / l,

[0079] carbolic acid 10mmol / l,

[0080] Ethylene glycol 50% (accounting for the total volume of the reagent).

[0081] Set on the automatic biochemical analyzer (Hitachi-7080): temperature 37°C, reaction time 10 minutes, test main wavelength 495-505nm, test secondary wavelength 600nm or more, the volume ratio of the tested sample to the reagent is 1:25, The reaction direction is positive reaction (absorbance rises, the same below).

[0082] Add the serum sample and the prepared single dose, and the two are automatically mixed in the analyzer, and the increase of the absorbance at 495-505...

Embodiment 2

[0083] Embodiment two (two doses)

[0084] Prepare the diagnostic kit for inorganic phosphorus in serum according to the following components and dosage:

[0085] Reagent I——

[0086] Imidazole ~ hydrochloric acid buffer 100mmol / l,

[0087] Nucleoside phosphatase 9000U / l,

[0088] Xanthine oxidase 9000U / l,

[0089] Urease 9000U / l,

[0090] Peroxidase 9000U / l,

[0091] 4-Aminoantiarsenic 1mmol / l,

[0092] Glycerol 50% (accounting for the total volume of reagent I);

[0093] Reagent II——

[0094] Imidazole ~ hydrochloric acid buffer 100mmol / l,

[0095] Inosine 5mmol / l,

[0096] 2,4,6-tribromo-3-hydroxy-benzenesulfonic acid 1mmol / l,

[0097] Dextran 50% (total volume of reagent II).

[0098] Set on the automatic biochemical analyzer (Hitachi-7080): temperature 30°C, reaction time 15 minutes, test main wavelength 546nm, test secondary wavelength 630nm or more, the ratio of the total volume of the tested sample to reagent I and reagent II is 1:25, the ratio of the amoun...

Embodiment 3

[0100] Embodiment three (three doses)

[0101] Prepare the diagnostic kit for inorganic phosphorus in serum according to the following components and dosage:

[0102] Reagent I——

[0103] Triethanolamine buffer 120mmol / l,

[0104] Xanthine oxidase 12000U / l,

[0105] Urease 12000U / l,

[0106] Peroxidase 12000U / l,

[0107] 3-methyl-2-benzothiazolone hydrazone 2mmol / l,

[0108] Propylene glycol 50% (accounting for reagent I gross volume);

[0109] Reagent II——

[0110] Triethanolamine buffer 120mmol / l,

[0111] Nucleoside phosphatase 12000U / l,

[0112] Dimethylaniline 2mmol / l,

[0113] Propylene glycol 50% (accounting for the total volume of reagent II);

[0114] Reagent III——

[0115] Triethanolamine buffer 120mmol / l,

[0116] Inosine 10mmol / l,

[0117] Mannitol 20mmol / l.

[0118] Set on the automatic biochemical analyzer (Hitachi-7080): temperature 25°C, reaction time 20 minutes, test main wavelength 578nm, test secondary wavelength 700nm or more, the total volume o...

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Abstract

The invention is about the measuring method of Inorganic Phosphates and its diagnosis reagent box. Producing hypoxanthine by reacting nucleoside phosphorylase with carnine under the existence of Inorganic Phosphates in the sample of plasma, serum and so on, then producing urate and hydroperoxide by reactinghypoxanthine withxanthine oxidase, and then reacting bimolecular hydroperoxide with peroxidaseand oxidating the colorless reduced chromogen combination to quinoneimine chromogen or indamide chromogen dyer with color, testing the variation of dominant wave-length400ú¡600nmabsorbance during the reaction and finally measuring the content of Inorganic Phosphates . This method has high specificity and would not be contaminated by material of internal and exogenous sources, and the result is precise and accurate. Using this method can realize the fast testing in common ultraviolet / visible light analyzer or semiautomatic / automatic analyzer and doesní»t require special or additional apparatus, so the cost is low. Thus, this method can be easily promoted and applied in the whole industry.

Description

technical field [0001] The invention relates to a method for measuring inorganic phosphorus and a diagnostic kit prepared by using the method, belonging to the technical field of medical examination and measurement. Background technique [0002] About 87% of the phosphorus in the human body exists in the bones, and the phosphorus in the blood maintains a dynamic balance relationship with the phosphorus in the bones. On the other hand, there is a certain relationship between the concentration of calcium and phosphorus in the blood, and the product of the two is kept within a certain range. In milligrams, the product of the content of calcium and phosphorus in about 100 ml of blood plasma is 35-40 . In normal people, when blood calcium increases, blood phosphorus decreases, and vice versa. When the above product is greater than 40, calcium and phosphorus are deposited in the bone tissue in the form of bone salt; when it is greater than 70, metastatic calcification may occur;...

Claims

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Application Information

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IPC IPC(8): C12Q1/28
Inventor 王尔中
Owner SUZHOU ANJ BIOTECHNOLOGY CO LTD
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