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Kit for quantitatively detecting cTnT/NT-proBNP/D-dimer and application thereof

A quantitative detection and kit technology, applied in biological tests, measurement devices, material inspection products, etc., can solve the problems of single diagnosis and few simultaneous detection methods, and achieve timely and targeted treatment and improve the effect of survival rate.

Pending Publication Date: 2022-02-11
广州达泰生物工程技术有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] 1. The detection methods for cTnI, NT-proBNP and D-dimer include enzyme-linked immunoassay, fluorescent immunoassay, chemiluminescence, immunoturbidimetry and colloidal gold immunochromatography, etc., but the detection products and methods are mainly Limited to the detection of one or two of them, there are very few methods for simultaneous detection of the three
[0008] 2. Most myocardial injuries are treated with cardiac troponin I / T (cardiac troponin I / cardiac troponinT, cTnT / T), creatine kinase-MB (CK-MB), myoglobin (myoglobin, MYO), these three joint tests, although very important, are relatively single in terms of diagnosis. For patients with non-cardiac chest pain, these three tests have certain limitations, especially for emergency departments. challenged

Method used

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  • Kit for quantitatively detecting cTnT/NT-proBNP/D-dimer and application thereof
  • Kit for quantitatively detecting cTnT/NT-proBNP/D-dimer and application thereof
  • Kit for quantitatively detecting cTnT/NT-proBNP/D-dimer and application thereof

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preparation example Construction

[0067] Second, the preparation method of the sample pad:

[0068] Soak the glass fiber membrane in the treatment solution containing 1.0% Triton X-100, 2.5% BSA, 0.15M Tris buffer, pH7.5, soak at 4°C for 4 hours, then place it in an oven and dry it at 37°C 2 hours.

[0069] Three, the preparation method of binding pad:

[0070] The bonding pad described in the application is prepared by the following steps:

[0071] Soak the glass fiber membrane in 150mM Tris-HCL treatment solution (containing 1.0% Triton X-100, 2.5% BSA, pH7.4), soak at 4°C for 2 hours, then take it out of the oven at 37°C and dry it for 4 hours for use. The glass fiber membrane was placed on the Bio-DotXYZ3050 three-dimensional spraying platform, and the rare earth fluorescent microspheres labeled anti-cardiac troponin T, anti-N-terminal atrial natriuretic peptide, and anti-D- Dimeric antibody and goat anti-chicken IgY antibody, the obtained anti-cardiac troponin T antibody-fluorescent microsphere couplin...

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Abstract

The embodiment of the invention belongs to the technical field of fluorescence immunochromatography, and relates to a kit for quantitatively detecting cTnT / NT-proBNP / D-dimer and application thereof, the kit comprises a detection card, the detection card comprises a card shell and a test paper card, the test paper card comprises a PVC bottom plate, and the PVC bottom plate is provided with a sample pad, a conjugate pad, a nitrocellulose membrane and absorbent paper; three monoclonal antibodies, namely anti-cardiac troponin T, anti-N-terminal atrial natriuretic peptide and anti-D dimer, which are respectively marked by rare earth Eu < 3 + > fluorescent microspheres, and a goat anti-chicken IgY antibody marked by rare earth Eu < 3 + > fluorescent microspheres are adsorbed on the combination pad; the nitrocellulose membrane is provided with a first detection line, a second detection line, a third detection line and a quality control line, the first detection line is coated with a D-dimer monoclonal antibody, the second detection line is coated with a cTnT monoclonal antibody, the third detection line is coated with an NT-proBNP monoclonal antibody, and the quality control line is coated with a chicken IgY antibody; and the cTnT, NT-proBNP and D-dimer can be rapidly, accurately and quantitatively detected at the same time through one-time sampling.

Description

technical field [0001] The application relates to the technical field of fluorescence immunochromatography, in particular to a kit for quantitatively detecting cTnT / NT-proBNP / D-dimer and its application. Background technique [0002] Chest pain is a common and life-threatening condition. The causes of chest pain are complex and diverse, including acute coronary syndrome (Acute Coronary Syndrome, ACS), acute aortic dissection (Acute Aortic Dissection, AAD) and acute pulmonary embolism (Acute Pulmonary Embolism). Pulmonary Embolism, APE), among which ACS accounts for the highest proportion of these serious life-threatening diseases. In recent years, its incidence rate has been increasing year by year, and the risk of death of patients is also increasing. How to quickly and accurately diagnose and differentiate the etiology of ACS and other fatal chest pains has become the difficulty and focus of emergency treatment. All patients with chest pain need to undergo an electrocardi...

Claims

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Application Information

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IPC IPC(8): G01N33/533G01N33/558G01N33/68G01N21/64
CPCG01N33/558G01N33/6893G01N33/533G01N21/6408G01N2333/58G01N2333/75G01N2800/329G01N2800/324
Inventor 石磊黎文娟邓成刚谢丽娟陈魏穗
Owner 广州达泰生物工程技术有限公司
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