Lange U, Nowak G, Bucha E
HaemoSys GmbH, Medical Faculty, Friedrich Schiller University, Jena, Germany.
Pathophysiol Haemost Thromb. 2003;33(4):184-91. doi: 10.1159/000081506.
A new sensitive and precise method for quantitative determination of direct thrombin inhibitors is described, the ecarin chromogenic assay (ECA). Ecarin is used as the specific prothrombin-activating principle. The cleavage of a chromogenic substrate by meizothrombin is inhibited in a concentration-dependent fashion by direct thrombin inhibitors. For the ECA, the linear measuring range is about 0.1-3.0 microg hirudin/ml plasma. Coefficients of variations between 2.3 and 4% over the whole concentration range were achieved. The ECA has proved to be more sensitive than the compared tests (ecarin clotting time and a thrombin-based chromogenic assay); a detection limit of 0.011 microg hirudin/ml and a quantitation limit of 0.032 microg hirudin/ml were calculated. The ECA is independent of the variations of the coagulation variables fibrinogen and prothrombin. Neither heparin nor oral anticoagulants interfere with the ECA.
本文描述了一种用于定量测定直接凝血酶抑制剂的灵敏且精确的新方法——蛇毒凝血酶显色法(ECA)。蛇毒凝血酶用作特异性凝血酶原激活剂。直接凝血酶抑制剂以浓度依赖方式抑制中间凝血酶对显色底物的裂解。对于ECA,线性测量范围约为0.1 - 3.0微克水蛭素/毫升血浆。在整个浓度范围内变异系数达到2.3%至4%。已证明ECA比对照试验(蛇毒凝血酶凝固时间和基于凝血酶的显色法)更灵敏;计算得出检测限为0.011微克水蛭素/毫升,定量限为0.032微克水蛭素/毫升。ECA不受凝血变量纤维蛋白原和凝血酶原变化的影响。肝素和口服抗凝剂均不干扰ECA。