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内源性凝血活性测定

The intrinsic coagulation activity assay.

作者信息

Stief Thomas W, Otto Stefanie, Renz Harald

机构信息

Department of Clinical Chemistry - Central Laboratory, University Hospital Giessen & Marburg, Germany.

出版信息

Blood Coagul Fibrinolysis. 2006 Jul;17(5):369-78. doi: 10.1097/01.mbc.0000233367.95733.d8.

Abstract

A new assay for the contact-phase-mediated generation of thrombin activity has been developed - the intrinsic coagulation activity assay (INCA). Citrated plasma (50 microl) is incubated with 5 microl SiO2, 250 mmol/l CaCl2 in polystyrole flat-bottom wells. After exactly 4 and 5 min (37 degrees C) coagulation reaction times (INCA-4 and INCA-5), 100 microl of 2.5 mol/l arginine, pH 8.6, is added to inhibit hemostasis activation in the important ascending part of the thrombin generation curve and to depolymerize fibrin. After 20 min, 50 microl of 1 mmol/l (final concentration 0.24 mmol/l) chromogenic thrombin substrate CHG-Ala-Arg-pNA in 1.25 mol/l arginine, pH 8.7, is added. The increase in absorbance is determined at 405 nm using a microtiterplate photometer. The assay is calibrated against 1 IU/ml thrombin. The normal thrombin activity range of INCA-4 (main value) or INCA-5 (control value) is 100 +/- 30% of normal (mean value +/- 1 SD; 100% = 0.5 IU/ml for INCA-4 and 1.9 IU/ml for INCA-5). With the INCA the normal range of intrinsic hemostasis is reflected, low-molecular-weight heparins can be monitored, the plasma matrix is not changed significantly, and the assay results are a percentage of normal generated thrombin activity and not coagulation seconds.

摘要

一种用于接触相介导的凝血酶活性生成的新检测方法已被开发出来——即内源性凝血活性检测(INCA)。将枸橼酸盐血浆(50微升)与5微升二氧化硅、250毫摩尔/升氯化钙在聚苯乙烯平底孔中孵育。在精确的4分钟和5分钟(37℃)凝血反应时间(INCA - 4和INCA - 5)后,加入100微升2.5摩尔/升、pH 8.6的精氨酸以抑制凝血酶生成曲线重要上升部分的止血激活并使纤维蛋白解聚。20分钟后,加入50微升1毫摩尔/升(终浓度0.24毫摩尔/升)的发色凝血酶底物CHG - Ala - Arg - pNA于1.25摩尔/升、pH 8.7的精氨酸中。使用酶标仪在405纳米处测定吸光度的增加。该检测以1国际单位/毫升凝血酶进行校准。INCA - 4(主要值)或INCA - 5(对照值)的正常凝血酶活性范围为正常的100±30%(平均值±1标准差;对于INCA - 4,100% = 0.5国际单位/毫升,对于INCA - 5,100% = 1.9国际单位/毫升)。通过INCA可以反映内源性止血的正常范围,可监测低分子量肝素,血浆基质没有显著变化,并且检测结果是正常生成的凝血酶活性的百分比而非凝血秒数。

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