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一种对血小板第4因子不敏感的改良肝素测定法。

An improved heparin assay which is insensitive to platelet factor 4.

作者信息

Fickenscher K, Buckler U

机构信息

Department for Blood Coagulation, Research Laboratories of Behringwerke AG, Marburg, FRG.

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1989;116(6):873-8.

PMID:2483705
Abstract

A new reagent for the determination of heparin in plasma has been developed. In the assay heparin which was bound to platelet factor 4 is also measured. That is why samples, which have to be assayed for heparin with this reagent, do not need any special pretreatment like fast and cooled processing in order to prevent release of platelet factor 4 from platelets. Heparin can be assayed in samples anticoagulated with citrate which are used routinely for the determination of other coagulation parameters like PT or aPTT. Freezing prior to the assay is possible and does not influence the result. The assay is based on the inactivation of factor Xa by antithrombin III which is catalysed by heparin or smaller fragments of it. It can therefore be used for the determination of heparins of low molecular weight, too. The sample is first mixed with AT III in order to compensate for a potentially decreased level in the probe. Then the F Xa reagent is added, which releases bound heparin from plasma proteins like platelet factor 4 by an added polysulfated dextran simultaneously to the onset of the inhibitory reaction towards F Xa. Free and secondarily released heparin are then available for determination. After a defined period of time a substrate for F Xa is added and the remaining activity is measured in a photometer. An incubation time of 1 min or 3 min is used for the normal range of 0.1 to 1 U/ml or the low dose range from 0.01 to 0.3 U/ml heparin, respectively.

摘要

已研发出一种用于测定血浆中肝素的新型试剂。在该测定法中,与血小板因子4结合的肝素也会被检测到。这就是为什么使用该试剂检测肝素的样本无需进行任何特殊预处理,如快速冷却处理,以防止血小板因子4从血小板中释放出来。肝素可以在用柠檬酸盐抗凝的样本中进行检测,这些样本通常用于测定其他凝血参数,如PT或aPTT。检测前冷冻是可行的,且不会影响结果。该测定法基于抗凝血酶III对因子Xa的灭活作用,此过程由肝素或其较小片段催化。因此,它也可用于测定低分子量肝素。首先将样本与抗凝血酶III混合,以补偿样本中可能降低的水平。然后加入因子Xa试剂,该试剂在对因子Xa的抑制反应开始时,通过添加的多硫酸化葡聚糖从血浆蛋白(如血小板因子4)中释放结合的肝素。游离的和二次释放的肝素随后可用于检测。在规定时间后,加入因子Xa的底物,并在光度计中测量剩余活性。对于肝素正常范围0.1至1 U/ml或低剂量范围0.01至0.3 U/ml,分别使用1分钟或3分钟的孵育时间。

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