Thromb Haemost 1994; 72(01): 105-112
DOI: 10.1055/s-0038-1648820
Original Article
Schattauer GmbH Stuttgart

Transport Phenomena and Clot Dissolving Therapy: An Experimental Investigation of Diffusion-Controlled and Permeation-Enhanced Fibrinolysis

Authors

  • Jung-He Wu

    1   The Bioengineering Laboratory, Department of Chemical Engineering, The State University of New York, NY, USA
  • Khalid Siddiqui

    2   Department of Medicine, Buffalo General Hospital, Buffalo, NY, USA
  • Scott L Diamond

    1   The Bioengineering Laboratory, Department of Chemical Engineering, The State University of New York, NY, USA
Further Information

Publication History

Received 06 January 1994

Accepted after revision 10 March 1994

Publication Date:
12 July 2018 (online)

Preview

Summary

We have investigated the effects of diffusive and convective transport on fibrinolysis. Using a constant pressure drop (ΔP/L) from 0 to 3.7 mmHg/cm-clot to drive fluid permeation, various regimes of lytic agents were delivered into fine and coarse fibrin gels (3 mg/ml) and whole blood clots. Using plasmin (1 μM) delivered into pure fibrin or urokinase (1 μM) delivered into glu-plasminogen (2.2 μM)-laden fibrin, the velocity at which a lysis front moved across fibrin was greatly enhanced by increasing ΔP/L. Lysis of fine and coarse fibrin clots by 1 μM plasmin at ΔP/L of 3.67 and 1.835 mmHg/cm-clot, respectively, led to a 12-fold and 16-fold enhancement of the lysis front velocity compared to lysis without pressure-driven permeation. For uPA-me-diated lysis of coarse fibrin at ΔP/L = 3.67 mmHg/cm-clot, the velocity of the lysis front was 25-fold faster than the lysis front velocity measured in the absence of permeation. Similar permeation-enhanced phenomenon was seen for the lysis of whole blood clots. Without permeation, the placement of a lytic agent adjacent to a clot boundary led to a reaction front that moved at a velocity dependent on the concentration of plasmin or uPA used. Overall, these studies suggest that transport phenomena within the clot can play a major role in determining the time needed for reperfusion during fibrinolysis.