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Hepatitis C virus antigen-antibody combined detection kit and detection method

A combined detection technology for hepatitis C virus, applied in the field of immune detection, can solve problems such as weakened capture ability, high quality control requirements, and errors, and achieve the effects of improving blood use and blood transfusion safety, improving work efficiency, and saving costs

Active Publication Date: 2014-03-12
山东莱博生物科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] 1. Hepatitis C antibody detection: It is the most widely used detection method at present, but its disadvantage is that there is a "window period". 66 days on average), at this time, blood donors have been infected and are infectious, and cannot be detected by current antibody detection reagents, this stage is called the window period before seroconversion (perseroconversion window phase, PWP).PWP The existence of HCV is one of the important threats to blood transfusion safety, so that blood recipients still have the risk of HCV infection after transfusion of blood that is negative for anti-HCV screening
[0006] 2. HCV RNA detection: It is mainly used for the selection of antiviral therapy and efficacy monitoring, but it needs to be operated in strict accordance with the PCR operating procedures, and the testing personnel need to be professionally trained and have corresponding qualifications, and the quality control requirements of the samples are high. Submit for inspection under low temperature conditions within 2 hours, and extract RNA aseptically, which is prone to errors caused by instruments, reagents, personnel, and the environment, resulting in false positives and false negatives
[0018] 1. Coating problem: Because the corresponding antigen and antibody are coated on the microwell plate at the same time, even if they do not react with each other, one protein will cover or dominate the other protein, and the other protein will be overwhelmed. The capture ability is greatly weakened, which greatly affects the target of simultaneous detection of hepatitis C antigen antibody
[0023] 3. If the test sample is positive, it is impossible to confirm whether it is hepatitis C antigen positive, hepatitis C antibody positive, or both positive, and it needs to be tested with other independent detection kits

Method used

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  • Hepatitis C virus antigen-antibody combined detection kit and detection method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Example 1 Preparation of Microwell Plates of Hepatitis C Virus Chimeric Antigen and Hepatitis C Virus Monoclonal Antibody

[0038] (1) Through the sequence analysis of HCV and the design of chimeras, reconstitute the chimeric antigens of HCV core antigen and other non-structural proteins, and clone monoclonal antibodies with different epitopes, so that the two cannot combine with each other when they are coated with antigens and antibodies at the same time , to avoid affecting the combination of the corresponding HCV antibody and HCV-cAg in the sample to be tested. After sequence analysis and chimera design, the preparation methods of antigens and monoclonal antibodies were operated according to the conventional methods in "Molecular Cloning".

[0039] A. Antigen preparation and purification identification

[0040] ① Extract the total RNA of HCV virus;

[0041] ② RT-PCR amplified and cloned the corresponding gene fragments of NS-3, NS-4 and Core;

[0042] ③ cloned in...

Embodiment 2

[0069] Embodiment 2 Preparation of sample diluent

[0070] The content of hepatitis C antibody is high in the blood, and the core region antigen used for detection of hepatitis C antibody has strong homologous and heterologous binding ability in vivo or in vitro, which can easily cause high background or even false positive, so it is used to detect hepatitis C antibody The required sample size is very small. Currently, the sample size of common hepatitis C antibody detection kits is generally 10ul. However, the content of hepatitis C antigen in the blood is very small, and the detection sample requires a lot of sample size. Currently, the commercialized hepatitis C antigen The sample volume requirement in the test kit is 100ul. Therefore, there is a certain contradiction in the sample size requirements when the two are tested at the same time.

[0071] In the present invention, by adding protein sedimentation agent, reducing agent, detergent, etc. to the sample diluent, the h...

Embodiment 3

[0090] Example 3 Preparation of Enzyme Working Solution and Detection Operation Process

[0091] (1) Preparation of enzyme-labeled protein: take an appropriate amount of horseradish peroxidase (according to 1mg protein plus 1mg HRP), dissolve 5mg HRP in 1.0ml NaHCO 3 solution to fully dissolve the HRP. Add appropriate amount of 0.06M NaIO 4 Stir at room temperature in the dark for 30 minutes. Transfer to a dialysis bag and dialyze overnight with 0.01M pH9.6 carbonate buffer. Take an appropriate amount of purified protein to be labeled, and use 0.01M NaHCO 3 The solution was fully dissolved, mixed with the enzyme solution, put into a dialysis bag, and dialyzed with 0.01M pH9.6 carbonate buffer solution at 4°C in the dark for 20 hours, and the medium was changed 3 times in the middle. Take the combined solution after dialysis, add 0.4% NaBH 4 (Based on the basis of 5mg HRP dissolved in 0.2ml NaBH4 solution) after stirring for 30 minutes, stand at 4°C for 4 hours. The enzym...

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PUM

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Abstract

The invention discloses a hepatitis C virus (HCV) antigen-antibody combined detection kit. The kit comprises a microwell plate coated with an HCV chimeric antigen and an HCV monoclonal antibody, a sample diluent, an HCV antigen-antibody combined detection enzyme working fluid, an HCV abzyme working fluid, an HCV antigen enzyme working fluid, a substance A fluid, a substance B fluid, a 20-times concentrated washing fluid and a stopping fluid. The invention also discloses preparation and usage of the key components of the kit, such as the microwell plate of the HCV chimeric antigen and the HCV monoclonal antibody, the sample diluent, and the diluent of enzyme working fluid. The kit and detection method, disclosed by the invention, are able to be used for detecting the HCV antigen and antibody at the same time, or individually detecting the situation of the HCV antigen during the early hepatitis c or the acute infection period, or before the antibody is produced, or when an antigen-antibody compound is produced, or individually detecting the situation of the HCV antibody after the antibody is produced; the kit and detection method can be applied to early HCV detection and therapy evaluation, so as to provide important detection evaluation index for clinical guideline.

Description

technical field [0001] The invention belongs to the technical field of immunoassay, and specifically relates to a hepatitis C virus (HCV) antigen-antibody combined detection kit and a detection method thereof. Background technique [0002] Hepatitis C is a global infectious disease caused by hepatitis C virus (HCV) infection. It is estimated that there are currently 170 million hepatitis C virus-infected people in the world, and the hepatitis C infection rate in my country is about 3.2%. At present, there are at least 40-60 million hepatitis C patients. The incidence of chronicity of hepatitis C is significantly higher than that of hepatitis B, and it is more prone to early liver cirrhosis than hepatitis B, leading to liver cancer and higher mortality rate, especially the early diagnosis of HCV is very important for screening the source of infection of HCV and guiding clinical practice. Treatment and prognosis are of great significance. Therefore, it is necessary to find a...

Claims

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Application Information

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IPC IPC(8): G01N33/577G01N33/531
CPCG01N33/54393G01N33/56983G01N33/5767G01N2333/186
Inventor 朱之炜吕红娟欧兰香王佳颖陈振王岩寇宗阳丁兴龙
Owner 山东莱博生物科技有限公司
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