Thromb Haemost 1978; 39(02): 426-436
DOI: 10.1055/s-0038-1646702
Original Article
Schattauer GmbH Stuttgart

Immobilization of Plasminogen Activator, Urokinase, on Nylon

Authors

  • Akio Sugitachi

    The Departments of Surgery, Osaka National Hospital, the Centre for Adult Diseases, Osaka, Osaka University Medical School and the Research and Development Centre, Unitika Ltd., Kyoto, Japan
  • Kunihiko Taragi

    The Departments of Surgery, Osaka National Hospital, the Centre for Adult Diseases, Osaka, Osaka University Medical School and the Research and Development Centre, Unitika Ltd., Kyoto, Japan
  • Shingi Imaoka

    The Departments of Surgery, Osaka National Hospital, the Centre for Adult Diseases, Osaka, Osaka University Medical School and the Research and Development Centre, Unitika Ltd., Kyoto, Japan
  • Goroh Kosaki

    The Departments of Surgery, Osaka National Hospital, the Centre for Adult Diseases, Osaka, Osaka University Medical School and the Research and Development Centre, Unitika Ltd., Kyoto, Japan
Further Information

Publication History

Received 10 November 1977

Accepted 06 October 1977

Publication Date:
12 July 2018 (online)

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Summary

Urokinase (UK), a fibrinolytic enzyme activator purified from human material was immobilized on nylon using different procedures. One was a modified method of immobilization of antigen or antibody initially carried out by Edelman and others in 1971 (Procedure I). The other was our newly devised method (Procedure II) (Sugitachi et al. 1976).

Major specificities of the immobilized UK are as follows:

1. The UK revealed properties of a plasminogen activator and the optimum pH of the immobilized UK was between 7.2 and 7.4, these values being in good parallel with that of soluble UK. The immobilized UK maintained a stable fibrinolytic activity after long-term preservation and heat-treatment.

2. As the fibrinolytic activity of immobilized UK was found to be inhibited by the antiplasmin in human plasma, an antiplasmin inhibitor was immobilized on the nylon together with the UK.

The antiplasmin activity was to some extent prevented using this procedure.

3. Nylon tubes immobilized with UK and antiplasmin inhibitor were used for thrombotic coagulation studies carried out according to the method of Chandler. Thrombus formation time (TFT) of UK-immobilized tubes was 30 min, while that of the non-treated tubes was no longer than 10 min.