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Activated partial thromboplastin generation combined correction test and detection kit

A technology of thromboplastin time and kit, which is applied in biological tests, measuring devices, analytical materials, etc., can solve the problems of inconsistent standards and cumbersome processes.

Pending Publication Date: 2022-03-18
周丽艳
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The method of the present invention draws lessons from the inspection methods before the 1990s: "Serum Prothrombin Generation and Correction Test", "Simple Thromboplastin Generation and Correction Test". The reagent production and detection methods of this method are all manually operated, and the process is cumbersome. , standards are not uniform, sensitivity and accuracy are low, and the application has long been discontinued

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0011] Reagent

[0012] Activated partial thromboplastin reagent: available in the market.

[0013] Barium Sulfate Adsorbed Plasma Production Method:

[0014] The blood of more than 10 normal people was collected, anticoagulated with 109mmol / L sodium citrate 1:9, centrifuged at 3000rpm for 10min, the upper layer plasma was drawn, and the plasma of more than 10 people was mixed to obtain fresh mixed plasma. Take a certain amount of mixed plasma in a container and add 100mg of dry barium sulfate per milliliter of plasma, and keep stirring in a water bath at 37°C for 15 minutes. The above liquid was centrifuged at 3000 rpm for 30 minutes, and the separated supernatant was barium sulfate-adsorbed plasma.

[0015] Preparation method of stored serum:

[0016] Take the blood of more than 10 normal people respectively, and naturally coagulate in the container. Put it in a 37°C incubator for 24 hours, take it out and centrifuge at 3000 rpm for 10 minutes, absorb the upper serum, an...

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PUM

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Abstract

The invention relates to a method for simultaneously detecting five hemorrhagic diseases clinically and a preparation method of a kit. The method is characterized by comprising the following steps: (1) preparing a kit containing fresh mixed plasma, barium sulfate adsorbed plasma and stored serum; and (2) adding a certain amount of plasma of a patient to be detected into each tube of the kit, and respectively detecting activated partial thromboplastin time (APTT) of each tube. The five hemorrhagic diseases are diagnosed in a laboratory according to the comparison condition (correction condition) of the APTT time of the reagent containing tube and the APTT time of the plasma of the patient. And (3) diluting the mixed plasma with different concentrations by using the stored serum and the barium sulfate adsorbed plasma respectively, determining activated partial thromboplastin time (APTT) to obtain standard curves of factors VIII and IX, and quantitatively determining the factors VIII and IX of the patient.

Description

technical field [0001] The invention relates to a test method and a test kit for in vitro diagnosis of hemorrhagic diseases. Background technique [0002] At present, various clinical bleeding disorders require different testing methods for screening, exclusion, and diagnosis, and multiple blood collection tests are required, which is troublesome, time-consuming, and costly. The method uses a kit for one person and uses a hemagglutination instrument to carry out laboratory diagnosis of five bleeding diseases, which avoids the disadvantages of multiple blood collections for a single test, prolonged diagnosis time, and high price. The sensitivity and accuracy of this method are high. [0003] The method of the present invention draws lessons from the inspection methods before the 1990s: "Serum Prothrombin Generation and Correction Test", "Simple Thromboplastin Generation and Correction Test". The reagent production and detection methods of this method are all manually operate...

Claims

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Application Information

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IPC IPC(8): G01N33/86
CPCG01N33/86G01N2800/224
Inventor 周丽艳
Owner 周丽艳
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