Clinical reagent kit D-Dimer for Automatic immunoassay analyzer in Cardiac Marker

CLIA Reagents of Inflammation (D-Dimer)

【Expected usage】
This product is used to quantitatively detect the content of D-dimer (D-Dimer) in human plasma in vitro.

D-dimer is a specific degradation product produced by plasmin hydrolysis after fibrin monomer is cross-linked by activating factor XIII. It is a specific marker of fibrinolysis process. D-dimers are derived from cross-linked fibrin clots lysed by plasmin.

The fibrinolytic system is the most important anticoagulant system in the human body and consists of four main components: plasminogen, plasminogen activator, plasmin, and plasmin inhibitor. When a fibrin clot is formed, in the presence of a plasminogen activator, plasminogen is activated and converted to plasmin, the fibrinolytic process begins, and plasmin degrades the fibrin clot to form various soluble fragments, forming Fibrin product, fibrin product consists of the following substances: X-oligomer, D-dimer, intermediate fragment, fragment E. Among them, X-oligomer and D-dimer both contain D-dimer units.

The human fibrinolytic system plays an important role in maintaining the normal permeability of the blood vessel wall, maintaining blood flow and tissue repair. Increased plasma levels of D-dimer indicate a secondary fibrinolytic process with thrombin production followed by activation of the fibrinolytic system. Thrombolytic therapy refers to the use of drugs to activate the fibrinolytic system. Generally, a plasminogen activator, such as urine enzyme, streptokinase or tissue-type plasminogen activator, is used to generate a large amount of plasmin, thereby accelerating the dissolution of thrombosis.

D-dimer mainly reflects fibrinolytic function. Increased or positive seen in secondary hyperfibrinolysis, such as hypercoagulable state, disseminated intravascular coagulation, renal disease, organ transplant rejection, thrombolytic therapy, etc. As long as there is active thrombosis and fibrinolysis in the body's blood vessels, D-dimer will increase. Myocardial infarction, cerebral infarction, pulmonary embolism, venous thrombosis, surgery, disseminated intravascular coagulation, infection and tissue necrosis can lead to elevated D-dimer. Especially for the elderly and hospitalized patients, due to bacteremia and other diseases, it is easy to cause abnormal blood coagulation and lead to increased D-dimer.
The current clinical and laboratory determination methods of D-dimer include enzyme-linked immunosorbent assay, colloidal gold method, fluorescence immunoassay, and chemiluminescence method.

【Inspection Principle】
This kit adopts the principle of direct sandwich method, uses magnetic microparticles as the solid phase of immune reaction, and uses chemiluminescence enzyme-linked immunosorbent assay method to cooperate with chemiluminescence measuring instruments to detect D-dimer (D-Dimer) in human plasma. )content.

The technical principle is: Fluorescein isothiocyanate (FITC)-labeled mouse monoclonal anti-D-Dimer antibody paired with alkaline phosphatase (AP)-labeled mouse monoclonal anti-D-Dimer antibody and samples, calibrators or The D-Dimer in the control product binds to form a "sandwich" complex. Subsequently, the magnetic particles linked with goat anti-fluorescein isothiocyanate (FITC) antibody were added, and the antigen-antibody immune complexes were bound to the magnetic particles through the specific binding of the anti-FITC antibody to FITC.

Under the action of an external magnetic field, the complex formed by the immune reaction is separated from other unbound substances, and after washing the complex, an enzymatic chemiluminescent substrate (adamantane derivative) is added. The substrate is catalytically cleaved under the action of the enzyme to form an unstable excited state intermediate.

When the excited state intermediate returns to the ground state, photons are emitted to form a luminescence reaction, and the luminescence intensity of the reaction can be detected by a chemiluminescence instrument. In the range of measurement wavelength (230-700nm), the luminescence intensity is proportional to the content of D-Dimer in the sample, and the D-Dimer concentration in the sample can be calculated by fitting the modified four-parameter Logistic equation.