Becker U, Jering H, Bartl K, Jilek F
Clin Chem. 1984 Apr;30(4):524-8.
We modified a test for prothrombin time, to automate its performance by centrifugal analysis. The sample is activated with calcium-thromboplastin in the presence of a thrombin-specific chromogenic peptide substrate, Tos-Gly-Pro-Arg-p-nitroaniline (Chromozym TH). The endpoint of the reaction is set as the time after onset until a defined amount of substrate has been cleaved, as reflected in a fixed change in absorbance. The assay is as sensitive as clotting-type methods are to the clotting factors of the extrinsic pathway--except for fibrinogen, which can be estimated from the maximum absorbance difference. Substrate concentration has little effect on the result, and varying it does not significantly change the sensitivity to factor X, which indicates little interference with the enzymes of the coagulation cascade. The method was applied to the Cobas Bio centrifugal analyzer. An external calculator must be used to convert absorbance readings into reaction times, which can be expressed as percent-of-normal values or as "ratios" by use of reagent-specific factors. CVs were less than 2% within run, less than 6% day to day. Overall correlation with the clotting test (r = 0.95) was good. Using the Cobas Bio, we achieved a throughput rate of 200 samples per hour.
我们改进了凝血酶原时间检测方法,通过离心分析实现其自动化操作。在凝血酶特异性显色肽底物Tos-Gly-Pro-Arg-p-硝基苯胺(Chromozym TH)存在的情况下,用钙组织凝血活酶激活样本。反应终点设定为从反应开始到一定量底物被裂解后的时间,这可通过吸光度的固定变化反映出来。该检测方法对外源性途径凝血因子的敏感性与凝血型方法相同——除纤维蛋白原外,纤维蛋白原可从最大吸光度差值估算得出。底物浓度对结果影响很小,改变底物浓度不会显著改变对因子X的敏感性,这表明对凝血级联反应的酶干扰很小。该方法应用于Cobas Bio离心分析仪。必须使用外部计算器将吸光度读数转换为反应时间,反应时间可以用正常数值的百分比表示,或通过使用试剂特异性因子表示为“比值”。批内变异系数小于2%,日间变异系数小于6%。与凝血检测的总体相关性良好(r = 0.95)。使用Cobas Bio,我们实现了每小时200个样本的检测通量。