DETERMINATION OF THROMBIN AND PLASMIN ACTIVITY IN HUMAN BLOOD PLASMA USING THE TURBIDIMETRIC CURVE OF CLOT FORMATION AND DISSOLUTION

A. V. Udovenko
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Abstract

The aim of the study was to develop a method for determination the activity of thrombin, which is based on the turbidimetry curve of the formation and dissolution of a blood plasma clot. Methods. Donor blood samples were collected in 3.8% sodium citrate (1 part of sodium citrate and 9 parts of blood, pH 7.4). Plasma was separated from blood cells within 1 hour after blood collection by centrifugation the latter at 1200 g for 20 minutes. Aliquots of plasma were stored at -20 °C. Results. To determine the concentrations of thrombin and plasmin, TDCs of the formation and dissolution of blood plasma clots, initiated by the APTT reagent, were used. Based on the values of τ obtained, a calibration curve was constructed in the coordinates 1/τ – [Thr] (the rate of protofibrils formation in s-1 vs thrombin concentration in NIH units in 1 ml). Conclusion. The proposed methods to determine the activity of thrombin and plasmin made it possible to quantitatively calculate the rate of prothrombin activation in the lag period, the concentration and activity of thrombin based on the rate of fibrin and protofibrils formation as well as the activity and concentration of plasmin at the point of the complete clot dissolution,
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用凝块形成和溶解浊度曲线测定人血浆中凝血酶和纤溶酶活性
本研究的目的是开发一种测定凝血酶活性的方法,该方法基于血浆凝块形成和溶解的浊度曲线。方法。在3.8%的柠檬酸钠(1份柠檬酸钠和9份血液,pH 7.4)中采集供体血液样本。在血液采集后1小时内,通过将血细胞以1200g离心20分钟从血细胞中分离血浆。血浆等分试样在-20°C下储存。后果为了测定凝血酶和纤溶酶的浓度,使用了由APTT试剂引发的血浆凝块形成和溶解的TDCs。基于获得的τ值,在坐标1/τ–[Thr](s-1中原纤维形成的速率与1ml中NIH单位中凝血酶浓度)中构建了校准曲线。结论所提出的测定凝血酶和纤溶酶活性的方法使得可以定量计算滞后期凝血酶原活化的速率、基于纤维蛋白和原纤维形成的速率的凝血酶的浓度和活性以及在完全溶解凝块时纤溶酶的活性和浓度,
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审稿时长
20 weeks
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