首页> 外国专利> Test system for the determination of in-vivo active hemostasis proteases or of trypsin or subtilisin in biological fluids and/or the usage thereof to determine the in-vivo activation of hemostasis or to diagnose a pancreatitis

Test system for the determination of in-vivo active hemostasis proteases or of trypsin or subtilisin in biological fluids and/or the usage thereof to determine the in-vivo activation of hemostasis or to diagnose a pancreatitis

机译:用于确定生物流体中体内活性止血蛋白酶或胰蛋白酶或枯草杆菌蛋白酶的测试系统和/或其用于确定体内止血激活或诊断胰腺炎的用途

摘要

Test system for the determination of in-vivo active hemostasis proteases or of trypsin or subtilisin in biological fluids and the usage thereof to determine the in-vivo activation of hemostasis or to diagnose a pancreatitis. ;The present invention describes a global assay of in vivo coagulation activation (GACA), i.e. the global determination of the in vivo activation of hemostasis, particularly of the in vivo activation of coagulation, of biological fluids, particularly of blood and/or plasma and the determination of in-vivo active trypsin and/or subtilisin. The sample to be tested, preferably a sample anticoagulated with EDTA and/or arginine (or guanidine), is incubated according to the invention with a chromogenic or fluorogenic substrate, particularly for Thrombin and/or Factor Xa and/or other enzymes of hemostasis in presence and/or absence of a contact activator and preferably in presence of EDTA. By detection of the absorbance, fluorescence and/or extinction of samples before and after the incubation the in-vivo activation of hemostasis of the biological fluid or the severity of a pancreatitis is determined. The resulting activity is compared with a known standard and indicated in percent of norm in relation to a 100% normal standard human plasma. The normal range is 100%±50% (mean±2 standard deviations). The GACA-activity of normal human plasma corresponds to a pure standard of 6 mlU/ml Thrombin.
机译:用于确定生物流体中体内活性止血蛋白酶或胰蛋白酶或枯草杆菌蛋白酶的测试系统及其在确定体内止血激活或诊断胰腺炎中的用途。本发明描述了体内凝结激活(GACA)的整体测定法,即对生物流体,特别是血液和/或血浆的止血的体内激活,特别是凝结的体内激活的整体测定。体内活性胰蛋白酶和/或枯草杆菌蛋白酶的测定。根据本发明,将待测试的样品,优选用EDTA和/或精氨酸(或胍)抗凝的样品,与发色或发荧光的底物一起温育,特别是用于凝血酶和/或因子Xa和/或其他止血酶。存在和/或不存在接触活化剂,优选在EDTA存在下。通过在温育之前和之后检测样品的吸光度,荧光和/或消光,确定生物流体止血或胰腺炎的严重程度的体内激活。将所得活性与已知标准进行比较,并以相对于100%正常标准人血浆的标准百分数表示。正常范围是100%加上50%(平均2个标准差)。正常人血浆的GACA活性对应于6 mlU / ml凝血酶的纯标准品。

著录项

  • 公开/公告号US2003044876A1

    专利类型

  • 公开/公告日2003-03-06

    原文格式PDF

  • 申请/专利权人 STIEF THOMAS W.;

    申请/专利号US20020115177

  • 发明设计人 THOMAS W. STIEF;

    申请日2002-04-02

  • 分类号C12Q1/37;C12Q1/00;

  • 国家 US

  • 入库时间 2022-08-22 00:07:54

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