THROMBIN GENERATION DETERMINATION METHOD
    7.
    发明授权
    THROMBIN GENERATION DETERMINATION METHOD 有权
    血栓形成的确定方法

    公开(公告)号:EP2529221B1

    公开(公告)日:2017-12-20

    申请号:EP11737503.0

    申请日:2011-01-25

    IPC分类号: G01N33/50 C12Q1/56

    CPC分类号: C12Q1/56

    摘要: A method for measuring a generation of thrombin in a sample of whole blood as a function of time includes adding to a sample of whole blood a fluorogenic substrate and a thrombin activator to form an activated sample. A conversion product is permitted to form in the activated sample. Fluorescence is measured as a function of time from a fluorescent group that is released during the formation of the conversion product with the use of a fluorescence detector. The fluorescence detector operates in an extended range mode and has an increased sensitivity. Thrombin generation as a function of time can then be calculated from the measured fluorescence as a function of time.

    IMPROVED CLOTTING COMPOSITION
    9.
    发明公开
    IMPROVED CLOTTING COMPOSITION 审中-公开
    改进的编制组成

    公开(公告)号:EP3209323A1

    公开(公告)日:2017-08-30

    申请号:EP15852949.5

    申请日:2015-10-23

    申请人: Q-Sera Pty Ltd

    摘要: The present invention relates to improved clotting compositions for producing high quality blood serum samples for analyte testing, such as for pathology testing and other biological assays. In particular, the present invention relates to the use of prothrombin activators in combination with stabilizing agents such as colloids for producing high quality blood serum samples. The present invention also relates to associated methods for preparing clotting compositions, tubes, kits and methods of diagnosis, prognosis and monitoring for responsiveness to therapy.

    摘要翻译: 本发明涉及用于生产用于分析物测试的高质量血清样品例如用于病理学测试和其他生物测定的改进的凝血组合物。 具体而言,本发明涉及凝血酶原激活剂与稳定剂如胶体组合用于生产高质量血清样品的用途。 本发明还涉及用于制备凝结组合物,试管,试剂盒以及诊断,预后和监测对治疗响应性的方法的相关方法。

    METHODOLOGIES AND REAGENTS FOR DETECTING FIBRINOLYSIS AND HYPERFIBRINOLYSIS
    10.
    发明公开
    METHODOLOGIES AND REAGENTS FOR DETECTING FIBRINOLYSIS AND HYPERFIBRINOLYSIS 审中-公开
    方法:联合化疗联合化疗联合维生素

    公开(公告)号:EP3140650A1

    公开(公告)日:2017-03-15

    申请号:EP14734284.4

    申请日:2014-05-05

    IPC分类号: G01N33/49 G01N33/86

    CPC分类号: G01N33/86 C12Q1/56 G01N33/49

    摘要: In some embodiments, the invention provides methods for detecting fibrinolysis or hyperfibrinolysis in a blood sample from a patient. The method includes subjecting a first portion of a blood sample comprising reduced platelet function to viscoelastic analysis in the absence of an inhibitor of fibrinolysis to obtain a coagulation characteristic of the first portion at a time point; and subjecting a second portion of the blood sample comprising reduced platelet function to viscoelastic analysis in the presence of an inhibitor of fibrinolysis to obtain a coagulation characteristic of the second portion at the time point; wherein a difference between the coagulation characteristic of the first portion and the coagulation characteristic of the second portion indicates fibrinolysis or hyperfibrinolysis in the blood sample.

    摘要翻译: 在一些实施方案中,本发明提供了用于在来自患者的血液样品中检测纤维蛋白溶解或超纤维蛋白溶解的方法。 所述方法包括在不存在纤维蛋白溶解抑制剂的情况下使包含减少血小板功能的血液样品的第一部分进行粘弹性分析,以在时间点获得第一部分的凝结特征; 并且在纤维蛋白溶解抑制剂存在的情况下使包含减少的血小板功能的血液样品的第二部分进行粘弹性分析,以获得在该时间点的第二部分的凝结特征; 其中第一部分的凝固特性与第二部分的凝固特性之间的差异表示血液样品中的纤维蛋白溶解或超纤维蛋白溶解。