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Dry chemistry test paper for quantitative determination of urea content in human blood

A technology for quantitative determination of urea content, applied in biological testing, color/spectral property measurement, material inspection products, etc., can solve the problems of complex production process, expensive reagents, hindering the widespread application of dry chemical products, etc.

Active Publication Date: 2012-10-10
SHANGHAI KEHUA BIO ENG
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0009] Some of the above products have complex production processes, such as Roche test strips; some require specialized equipment and technology, such as Johnson & Johnson and Fuji dry tablets
In particular, its reagents are expensive and can only be used in large hospitals, and are difficult to be accepted by small and medium hospitals, especially small hospitals, hindering the general application of dry chemical products
Moreover, the dry biochemical analyzers used in conjunction with it are mostly large and medium-sized instruments, which have certain limitations in terms of price and portability.

Method used

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  • Dry chemistry test paper for quantitative determination of urea content in human blood
  • Dry chemistry test paper for quantitative determination of urea content in human blood
  • Dry chemistry test paper for quantitative determination of urea content in human blood

Examples

Experimental program
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Embodiment 1

[0024]Embodiment 1: The upper, middle and lower support layers are made of PVC material, the thicknesses are respectively 0.14mm, 0.12mm and 0.14mm; the length is 20cm, and the width is 8cm. Wherein the upper and lower supporting layers are attached with viscose glue on one side, and the middle supporting layer is attached with viscose glue on both sides. Punch a sample hole, a vent hole and a test hole at one end respectively, the hole diameter is 4mm, and the hole distance is 8mm. The diffusion layer is made of nylon mesh, the reagent layer is made of fiber fabric, and the chromogenic layer is made of nitrocellulose membrane with plastic backing, all of which are 8mm wide. Paste the diffusion layer, the reagent layer and the chromogenic layer to the corresponding positions of the upper, middle and lower support layers respectively, that is, at the sample injection hole, the ventilation hole and the test hole. Then the upper support layer and the middle support layer are ali...

Embodiment 2

[0034] Embodiment 2: The upper, middle, and lower support layers are made of PET, with thicknesses of 0.12 mm, 0.15 mm, and 0.12 mm; the length is 20 cm, and the width is 8 cm. Wherein the upper and lower supporting layers are attached with viscose glue on one side, and the middle supporting layer is attached with viscose glue on both sides. Punch out the air hole of the sample hole and the test hole at one end respectively, the hole diameter is 4mm, and the hole distance is 8mm. The diffusion layer is made of polyester mesh cloth, the reagent layer is made of filter paper material, and the chromogenic layer is made of nitrocellulose membrane with plastic backing, and the width is 8mm. Paste the diffusion layer, the reagent layer and the chromogenic layer to the corresponding positions of the upper, middle and lower support layers respectively, that is, at the sample injection hole, the ventilation hole and the test hole. Then the upper support layer and the middle support la...

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Abstract

The invention belongs to the technical field of in-vitro clinical diagnostic reagent, in particular to a dry chemistry test paper for quantitative determination of urea content in human blood. The test paper comprises an upper, a middle and a lower support layers and testing layers thereof and is separated into a hand-held area and a test area. The test area is composed of a diffusion layer, a reagent layer and a color reagent layer from the top down. A loading hole is arranged on the upper support layer, a test sample is introduced into the diffusion layer from the loading hole to penetrate into the reagent layer, then enzymatic reaction is carried out on the reagent layer, ammonia is generated by catalyzing urea by using urease, and under the alkaline environment, the generated ammonia spreads to the color reagent layer to perform color reaction with the indicator of ammonia. The variation of optical density can be measured with a reflectance spectrophotometer through a test hole onthe lower support layer. The test paper can be used to quantitatively test the urea content in human blood, provides basis for the diagnosis of renal function, and is suitable to be used in emergencyrooms of the hospitals.

Description

technical field [0001] The invention belongs to the technical field of in vitro clinical diagnostic reagents, in particular to a dry chemical test paper suitable for quantitatively measuring urea content in human blood. Background technique [0002] Urea is the end product of protein metabolism in the human body. Amino acids in the body are decomposed into α-keto acids and NH by deamination 3 , NH 3 Enter the urea cycle and CO in hepatocytes 2 This produces urea. The liver is the most important organ that produces urea. The amount of urea produced depends on dietary protein intake, tissue protein catabolism, and liver function. The urea produced in the liver is mainly excreted by the kidneys, and a small part is excreted by sweat. It is mainly filtered by the glomeruli and excreted with the urine. If kidney function is impaired, the glomerular filtration rate decreases and the concentration of urea in the blood increases. [0003] The urea content in blood is one of t...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N33/52G01N21/31
Inventor 宁绍华朱世成王缦
Owner SHANGHAI KEHUA BIO ENG
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