Thromb Haemost 2000; 84(06): 1017-1022
DOI: 10.1055/s-0037-1614165
Review Article
Schattauer GmbH

A Collaborative Study to Establish the 5th International Standard for Unfractionated Heparin

Elaine Gray
1   From the National Institute for Biological Standards and Control, Potters Bar, Hertfordshire, UK
,
A. Dawn Walker
1   From the National Institute for Biological Standards and Control, Potters Bar, Hertfordshire, UK
,
Barbara Mulloy
1   From the National Institute for Biological Standards and Control, Potters Bar, Hertfordshire, UK
,
Trevor W. Barrowcliffe
1   From the National Institute for Biological Standards and Control, Potters Bar, Hertfordshire, UK
› Author Affiliations
We would like to thank the participants of the study and the following manufacturers for their kind donation of candidate samples: Diosynth bv, 5340 BH Oss, The Netherlands; Crinos Industria Farmacobiologica SpA, 22079 Villa Guardia, Como, Italy; Laboratori Derivati Organici, SS 31 bis Trino, Italy; Leo Pharmaceutical Products Ltd, 55 Industriparken, DK-2750 Ballerup, Denmark; Pharmacia & Upjohn, 160 Industrial Drive, Franklin, Ohio 45005, USA; Scientific Protein Laboratories, 700 E Main Street, Waunakee, USA; New Zealand Pharmaceuticals Ltd, Palmerston North 5330, Linton, New Zealand.
Further Information

Publication History

Received 19 March 2000

Accepted after resubmission 10 July 2000

Publication Date:
13 December 2017 (online)

Summary

Twenty-four laboratories participated in a collaborative study to calibrate a replacement for the 4th International Standard for Unfractionated Heparin (82/502). Both candidate materials A and B, gave excellent intra- and inter-laboratory variations (majority of mean %gcv <10%) when assayed against the 4th International Standard. No major differences of potency estimates were found between methods, although the USP method generally gave lower potencies than the other methods and candidate B gave a greater variation between methods than A. Overall, this study showed that the differences between the candidates are marginal. Based on its narrower molecular weight profile, higher specific activity and slightly lower inter-method variation, candidate A, 97/578, was proposed and accepted in October, 1998, by the Expert Committee on Biological Standardisation of the World Health Organisation to be the 5th International Standard for Unfractionated Heparin with an assigned potency of 2031 IU/ampoule.

 
  • References

  • 1 Crafoord C. Heparin and post-operative thrombosis. Acta Chirurgica Scandinavica 1939; 82: 319.
  • 2 World Health Organisation, Expert Committee on Biological Standardisation. Bull Wld Hlth Org. 1947/1948; 01: 9-10.
  • 3 Thomas DP, Curtis AD, Barrowcliffe TW. A collaborative study designed to establish the 4th International Standard for Heparin. Thromb Haemost 1984; 52 (02) 148-53.
  • 4 Mulloy B, Gray E, Barrowcliffe TW. Characterisation of unfractionated heparin: Comparison of materials from the last 50 years. Thromb Haemost 2000; 84: 1052-6.
  • 5 Finney DJ. Statistical methods in biological assay. 3rd edn. London: Charles Griffin; 1978
  • 6 Kirkwood TBL. Geometric means and measures of dispersion. Biometrics 1979; 35: 908-9.
  • 7 Bangham DR, Woodward PM. A collaborative study of heparins from different sources. Bull WHO 1970; 42: 129-49.
  • 8 Altman DG. Practical statistics for medical research. 1st Edn. London: Chapman and Hall; 1991