 
         
         
         ABSTRACT
         
         In the fibrin gel permeability assay, fibrin formation depends on thrombin generated
            endogenously, giving greater physiological relevance. The present study evaluated
            the effects of three direct thrombin inhibitors (argatroban, bivalirudin, and lepirudin)
            and one indirect factor Xa inhibitor (danaparoid) on fibrin gel permeability. Fibrin
            gels were prepared by adding tissue factor, phospholipids, and CaCl2 to normal plasma mixed with one of the inhibitors. The permeability constant (Ks)
            was determined through flow measurements. At concentrations corresponding to plasma
            levels during antithrombotic therapy, argatroban, bivalirudin, and danaparoid led
            to similar increases in Ks, by 320 to 370% of the control; in contrast, almost no
            effect on Ks could be detected for lepirudin. At concentrations above the “plasma-like”
            levels, the dose–response curve for lepirudin was noticeably steep, whereas those
            for the other drugs were shallow. This study suggests that argatroban, bivalirudin,
            and danaparoid have comparable potential to inhibit thrombin or Xa and the consequent
            coagulation, rendering the fibrin network permeable. The lack of influence on fibrin
            gel permeability by lepirudin at the “plasma-like” levels may contradict the antithrombotic
            effect observed in therapy, but the sharp dose–response curve shown at higher drug
            concentrations corresponds with reports of bleeding complications from lepirudin with
            overdosages.
         
         
         
            
KEYWORDS
         
         
            Thrombin inhibitor - factor Xa inhibitor - fibrin gel permeability - in vitro
          
      
    
   
      
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Shu HeM.D. 
            Coagulation Research, Clinical Chemistry, L2-5tr, Karolinska University Hospital
            
            S-17176, Stockholm, Sweden
            
            Email: he_shu@yahoo.com