Wolf P, Grimley R
Haemostasis. 1983;13(2):113-8. doi: 10.1159/000214714.
Coagulation rates in fresh, normal, venous blood was investigated when a given volume of blood was allowed to contact various materials of equivalent surface area, at 22 degrees C, without disturbance. The coagulation rate was determined indirectly by measuring residual thrombin-clottable fibrinogen in cell-free supernatants after arresting coagulation at fixed time intervals with a Ca++-chelating type of anticoagulant and comparing the thrombin-clottable fibrinogen content of the test samples with control samples of blood anticoagulated immediately after venipuncture. In glass containers, after initial formation of the clot, progressive fibrin formation, measured by the rate of disappearance of thrombin-clottable fibrinogen, was found to take place as a gradual and linear progressive process not complete at 30 min after venipuncture with blood stored undisturbed at 22 degrees C. Various graft materials in tubular form were prepared to ensure equivalent blood surface contact. These were investigated for their influence on fibrinogen to fibrin conversion of fresh venous blood in a 15-min period at 22 degrees C. Fibrin formation was greatest in microvel pre-treated with clotting blood and decreased in the following order: microvel, woven Dacron, knitted dacron and Gore-tex. Gore-tex showed by far the least thrombogenicity of all the tested graft materials. We discuss our reasons for making our measurements under non-flow conditions and the reason for measuring fibrinogen to fibrin conversion rather than measuring platelet deposition on the various surfaces.
在22摄氏度下,让一定体积的新鲜、正常静脉血与各种具有相同表面积的材料接触,且不受干扰,以此来研究凝血速率。通过使用钙离子螯合型抗凝剂在固定时间间隔停止凝血后,测量无细胞上清液中残余的可被凝血酶凝固的纤维蛋白原,并将测试样品中可被凝血酶凝固的纤维蛋白原含量与静脉穿刺后立即抗凝的对照血样进行比较,从而间接确定凝血速率。在玻璃容器中,在最初形成凝块后,通过可被凝血酶凝固的纤维蛋白原消失速率来衡量的纤维蛋白的逐渐形成,被发现是一个逐渐的、线性的过程,在22摄氏度下不受干扰储存的血液静脉穿刺30分钟后仍未完成。制备了各种管状移植材料以确保血液表面积接触相同。研究了它们在22摄氏度下15分钟内对新鲜静脉血中纤维蛋白原向纤维蛋白转化的影响。在经凝血血液预处理的微孔聚乙烯上纤维蛋白形成最多,其顺序依次降低为:微孔聚乙烯、机织涤纶、针织涤纶和戈尔特斯。在所有测试的移植材料中,戈尔特斯的血栓形成性最小。我们讨论了在非流动条件下进行测量的原因,以及测量纤维蛋白原向纤维蛋白转化而非测量血小板在各种表面沉积的原因。