Harenberg J, de Vries J X, Weber E, Zimmermann R
Dtsch Med Wochenschr. 1984 Jun 15;109(24):951-4. doi: 10.1055/s-2008-1069304.
The coagulation-inhibiting effect of subcutaneously administered commercial and a low-molecular heparin was compared in healthy volunteers. Global clotting activity, measured as activated partial thromboplastin time as well as thrombin activity were inhibited almost equally by commercial and low-molecular heparin. Low-molecular heparin caused a ten-fold stronger inhibition of factor Xa. The effect on factor Xa increased nearly logarithmically with the injected dose. Half-life of heparin measured in terms of the inhibition of factor Xa was 5.5 hours for the low-molecular and 3.5 hours for the commercial preparation. These results indicate that low-molecular heparin has a high specificity in the inhibition of factor Xa. A lower dose of low-molecular heparin, administered once daily, may have an anti-thrombotic effect while reducing the risk of bleeding.
在健康志愿者中比较了皮下注射的市售肝素和低分子肝素的抗凝作用。以活化部分凝血活酶时间衡量的整体凝血活性以及凝血酶活性,受到市售肝素和低分子肝素的抑制程度几乎相同。低分子肝素对Xa因子的抑制作用强十倍。对Xa因子的作用几乎随注射剂量呈对数增加。以对Xa因子的抑制作用衡量,低分子肝素的半衰期为5.5小时,市售制剂为3.5小时。这些结果表明,低分子肝素在抑制Xa因子方面具有高特异性。每日一次给予较低剂量的低分子肝素可能具有抗血栓形成作用,同时降低出血风险。