Thromb Haemost 1982; 47(02): 109-113
DOI: 10.1055/s-0038-1657140
Original Article
Schattauer GmbH Stuttgart

A Comparison of Pentosan Polysulphate and Heparin II: Effects of Subcutaneous Injection

Authors

  • A-M Fischer

    The National Institute for Biological Standards and Control, Hampstead, London, U.K.
  • R E Merton

    The National Institute for Biological Standards and Control, Hampstead, London, U.K.
  • N A Marsh

    The National Institute for Biological Standards and Control, Hampstead, London, U.K.
  • S Williams

    The National Institute for Biological Standards and Control, Hampstead, London, U.K.
  • P J Gaffney

    The National Institute for Biological Standards and Control, Hampstead, London, U.K.
  • T W Barrowcliffe

    The National Institute for Biological Standards and Control, Hampstead, London, U.K.
  • D P Thomas

    The National Institute for Biological Standards and Control, Hampstead, London, U.K.
Further Information

Publication History

Received 06 November 1981

Accepted 21 January 1982

Publication Date:
13 July 2018 (online)

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Summary

A comparison has been made between the effects of pentosan polysulphate (SP54) and mucosal heparin following subcutaneous injection in man. Unlike heparin, pentosan polysulphate has relatively little effect in vivo as measured by anti-factor Xa clotting assay and none by an anti-Xa amidolytic assay (S-2222). However, pentosan polysulphate is at least as potent as heparin on a weight basis in producing activation of lipoprotein lipase, shortening of the euglobulin clot lysis time and impairing the generation of factor Xa. Our data indicate that pentosan polysulphate has more marked effects in vivo than in vitro, that the action of the drug on clotting is mediated mainly via an At III-independent pathway, and that its effects are not confined to the coagulation system.