阅读说明：本技术 一种用于尿酸定量检测的干片试剂 (Dry tablet reagent for quantitative detection of uric acid ) 是由 郑日记 黄利寒 甘斌 武伟民 李菁杨 于 2019-10-31 设计创作，主要内容包括：本发明提供一种用于尿酸定量检测的干片试剂,包括外壳,所述外壳内依次贴合有扩散层、试剂层、树脂层、基材,所述外壳上表面中心位置开有样品滴加孔,底部中心位置开有透光孔,所述扩散层、试剂层、树脂通过涂布工艺从上到下依次分层贴合在基材上,所述该扩散层主要由二氧化钛、醋酸纤维素组成,所述试剂层主要包括尿酸酶、过氧化物酶、色素、缓冲液、交联剂、凝胶、酶保护剂。通过本发明,以解决现有技术存在的湿化学检测试剂不稳定、测试结果误差较大的问题。(The invention provides a dry plate reagent for quantitative detection of uric acid, which comprises a shell, wherein a diffusion layer, a reagent layer, a resin layer and a base material are sequentially attached to the shell, a sample dripping hole is formed in the center of the upper surface of the shell, a light transmission hole is formed in the center of the bottom of the shell, the diffusion layer, the reagent layer and the resin are sequentially attached to the base material in a layered mode from top to bottom through a coating process, the diffusion layer mainly comprises titanium dioxide and cellulose acetate, and the reagent layer mainly comprises uricase, peroxidase, a pigment, a buffer solution, a cross-linking agent, gel and an enzyme protective agent. The invention solves the problems of unstable wet chemical detection reagent and larger error of test result in the prior art.)

1. The utility model provides a dry piece reagent for uric acid quantitative determination, a serial communication port, includes shell (6), laminating diffusion layer (2), reagent layer (3), resin layer (4), substrate (5) in proper order in the shell, shell (6) upper surface central point puts to open there is sample dropwise add hole, and bottom central point puts to open there is the light trap, lamination laminating in proper order on the substrate from the top down through coating process is passed through in diffusion layer (2), reagent layer (3), resin (4), this diffusion layer (2) mainly comprises titanium dioxide, cellulose acetate, reagent layer (3) mainly include uricase, peroxidase, pigment, buffer solution, cross-linking agent, gel, protection enzyme agent.

2. The dry sheet reagent for uric acid quantitative determination according to claim 1, characterized in that the resin layer (4) is an aqueous epoxy resin.

3. The dry plate reagent for uric acid quantitative determination according to claim 1, wherein the substrate (5) is pet material for providing a skeleton for supporting reagents, and the transparency of the substrate is more than 80%.

4. The dry plate reagent for uric acid quantitative determination according to claim 1, wherein the casing (6) is made of plastic material for protecting the reagent from deformation caused by various external forces during transportation, storage and testing, thereby avoiding damage to the reagent.

5. The dry plate reagent for uric acid quantitative determination according to claim 1, characterized in that the diffusion layer (2) uses cellulose acetate as a three-dimensional network skeleton, and the three-dimensional network skeleton is wrapped with the corresponding reagent.

6. The dry sheet reagent for uric acid quantitative determination according to claim 1, characterized in that the reagent layer (3) is formed by coating the corresponding reagent with coagulated and dried gelatin as a carrier.

Technical Field

The invention relates to a uric acid detection reagent, in particular to a dry tablet reagent for quantitative detection of uric acid.

Background

So-called "dry-patch reagents" are relatively conventional "wet chemistry". The method is a mode that liquid in a detected sample is used as a reaction medium, and an object to be detected directly reacts with a reagent fixed on a carrier, and the method is different from the traditional wet chemistry in the medium participating in the chemical reaction. With the development of techniques for separation, purification, storage, etc. of enzymes in biochemistry, the progress of sensor, photometer, and electrode techniques, and the popularization of computers, dry chemistry has also rapidly developed.

Dry chemistry has unique advantages over wet chemistry, and as for reagents, dry chemistry reagents do not need preparation before measurement, do not need calibration, and are stable, and whole blood can be directly measured; as for the instrument, a water supply and drainage system and a pure water system are not required, so that the operation is simple and the maintenance is easy.

Disclosure of Invention

The invention provides a dry sheet reagent for quantitative detection of uric acid, which solves the problems of unstable wet chemical detection reagent and large error of test result in the prior art.

In order to solve the technical problems, the invention provides a dry plate reagent for quantitative detection of uric acid, which comprises a shell, wherein a diffusion layer, a reagent layer, a resin layer and a base material are sequentially attached to the shell, a sample dripping hole is formed in the center of the upper surface of the shell, a light transmission hole is formed in the center of the bottom of the shell, the diffusion layer, the reagent layer and the resin are sequentially attached to the base material in a layering manner from top to bottom through a coating process, the diffusion layer mainly comprises titanium dioxide and cellulose acetate, and the reagent layer mainly comprises uricase, peroxidase, a pigment, a buffer solution, a cross-linking agent, gel and an enzyme protective agent.

The resin layer is a water-based epoxy resin.

The substrate is a pet material for providing a skeleton for supporting the reagent, the substrate having a transparency greater than 80%.

The shell is made of plastic and is used for protecting the reagent from deformation caused by various external forces in the processes of transportation, storage and testing, so that the reagent is prevented from being damaged.

The diffusion layer takes cellulose acetate as a three-dimensional network framework, and the three-dimensional network framework is wrapped with a corresponding reagent.

The reagent layer is formed by coating corresponding reagents with coagulated and dried gelatin as a carrier.

The invention has the following beneficial effects: the dry tablet reagent is used for testing the uric acid by a dry chemical method on the basis of wet chemistry, has excellent performance, long storage time and accurate test result, can obviously improve various performance indexes of the uric acid in the detection and storage processes, and makes up for the deficiency of the wet chemistry.

Drawings

FIG. 1 is a schematic sectional structure diagram of a dry plate reagent for quantitative detection of uric acid according to the present invention.

FIG. 2 is a schematic diagram of the overall structure of the dry tablet reagent.

Wherein, 1-sample, 2-diffusion layer, 3-reagent layer, 4-resin layer, 5-substrate, and 6-shell.

Detailed Description

In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention will be described in further detail below with reference to the accompanying drawings and specific embodiments.

The invention provides a dry tablet reagent which is established on the basis of wet chemistry and is used for a dry chemical method for testing uric acid, and the dry tablet reagent can obviously improve various performance indexes of uric acid in the detection and storage processes and make up for the deficiency of wet chemistry.

As shown in fig. 1, the reagent dry sheet comprises:

and the diffusion layer 2 comprises necessary materials such as titanium dioxide and cellulose acetate and has the main functions of uniformly diffusing the sample, filtering macromolecular substances and interfering substances in the sample. The diffusion layer 2 is a three-dimensional network framework made of cellulose acetate, the three-dimensional network framework is wrapped with corresponding reagents such as titanium dioxide, and the structure of the diffusion layer is similar to that of a sponge and is wrapped with corresponding reagents such as titanium dioxide. The content of each diffusion layer component in each dry sheet is as described in table 1 below:

table 1: table of contents of components of diffusion layer

Name of reagent	Content per tablet (unit g)
		Cellulose acetate	0.0025
Titanium dioxide	0.03
		Surface active agent	0.00023
Magnesium chloride	0.00122
		Glycerol	0.0005
Polyethylene glycol	0.0005

And a reagent layer 3, which mainly comprises uricase, peroxidase, pigment, buffer solution, a cross-linking agent, gel, an enzyme protective agent and other necessary biochemical reagents. The reagent layer is formed by wrapping corresponding reagents by using coagulated and dried gelatin as a carrier, and the structure of the reagent layer is similar to that of jelly; the contents of the components of the reagent layer in each dry tablet are shown in table 2:

table 2: table of contents of each component of reagent layer

Name of reagent	Each tablet content
		Uricase	0.04U
Peroxidase enzymes	0.6U
		Imidazole dyes	0.0002MG
Tris buffer	25UL
		Polyacrylamide	0.03667G
Polyvinylpyrrolidone	0.0453G
		Gelatin	0.083G
EDTA	0.01667G
		Triton-100	0.00064G

Resin layer 4, this resin layer can be effectual makes reagent layer adhere to on the substrate, can reduce the requirement to the material and the performance of substrate, can use the substrate of not doing any processing, avoids handling the interference of substrate to detect reagent, and the resin layer is waterborne epoxy, and the structure is similar ordinary liquid glue, and the purchase of former factory is used directly.

A substrate 5, which mainly provides a skeleton supporting the reagents, the transparency of which must be greater than 80%, the substrate being pet material, structured like a hard plastic paper sheet.

The shell 6, this shell layer is mainly that the protection reagent is in the transportation, stores, and the deformation that the in-process of test leads to because various power to avoid the damage of reagent, especially in last machine test, no matter be automatic or semi-automatic send into the detection machine with the dry film reagent in, the dry film inevitably receives corresponding power, and the reagent shell can avoid the damage of reagent dry film. The housing 6 is plastic and the overall structure of the dry tablet reagent is shown in figure 2.

The preparation method of the dry tablet reagent comprises the following steps:

preparing a resin material to be coated on a base material;

coating reagent on the resin, wherein the reagent layer has different coating methods according to the needs and the process;

a diffusion layer is coated on the reagent.

In summary, the reagent is coated on the transparent plastic film in the form of a film to be made into a dry sheet, and the dry sheet reagent corresponding to the concentration of the target substance is obtained by detecting the reflected light. The dry chemical reagent prepared by the method has excellent performance and long storage time.

The specific operation of the dry-plate reagent detection is as follows: as shown in fig. 1, 10ul of sample 1 to be tested is added to the surface of the diffusion layer, the sample 1 can be uniformly diffused downwards horizontally and longitudinally through the diffusion layer, and enters the reagent layer, the target substance uric acid in the sample reacts with the corresponding substance in the dry slice, and the color change is generated, the reaction equation is shown in table 3, and the reaction process is specifically that uric acid in the sample is oxidized to generate hydrogen peroxide and allantoin under the catalysis of uricase. The peroxidase then catalyzes the oxidative coupling reaction of the dye precursor to produce a dye. The intensity of the dye is measured by reflected light and is in direct proportion to the concentration of glucose in the blood and urine. After sample adding, using 760nm light to irradiate to the central position of the substrate, recording the change of the reflected light of the dry plate after sample adding, wherein the reflected light density is inversely proportional to the concentration layer of the target substance uric acid, and calculating the corresponding concentration, namely the detection concentration of the sample corresponding to the uric acid through a computer.

Table 3: uric acid reaction equation

Reaction type

The above description is only an example of the present invention, and is not intended to limit the present invention, and it is obvious to those skilled in the art that various modifications and variations can be made in the present invention. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the scope of the claims of the present invention.