Thromb Haemost 1995; 74(03): 893-899
DOI: 10.1055/s-0038-1649843
Original Article
Coagulation
Schattauer GmbH Stuttgart

A Collaborative Study of Proposed European Pharmacopoeia Reference Preparations of Low Molecular Mass Heparin

Authors

  • E Gray

    The National Institute for Biological Standards and Control, South MImms, Potters Bar, Hertfordshire, UK
  • A B Heath

    The National Institute for Biological Standards and Control, South MImms, Potters Bar, Hertfordshire, UK
  • B Mulloy

    The National Institute for Biological Standards and Control, South MImms, Potters Bar, Hertfordshire, UK
  • J-M Spiese

    1   The European Pharmacopoeia Commission, Strasbourg, France
  • T W Barrowcliffe

    The National Institute for Biological Standards and Control, South MImms, Potters Bar, Hertfordshire, UK
Further Information

Publication History

Received 13 February 1995

Accepted after revision 08 May 1995

Publication Date:
26 July 2018 (online)

Preview

Summary

A European collaborative study, in which 16 laboratories participated, was carried out to assess the performance of the European Pharmacopoeia (EP) monograph methods for anticoagulant activities (anti-Xa and anti-IIa assays) of low molecular mass (EMM) heparin and to assess the suitability of six candidate materials as the EP working standard for LMM heparin. There was good interlaboratory agreement for both types of assays as indicated by most gcv’s being less than 10%, indicating acceptable performance of the EP assay methods. All the candidate preparations gave dose-response curves parallel to the 1st International Standard for Low Molecular Weight heparin and to each other. All preparations, possibly with the exception of E and F, gave similar performance as measured by interlaboratory agreement and would be suitable as working standards. Based on these data, preparations A, B, C and D have been established by the EP as official EP Biological Reference Preparations and they will be issued as successive batches.