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An evaluation of the British Pharmacopoeial assay of heparin: a comparison with other methods.
  1. G A Shah,
  2. T Z Dhall,
  3. I Ferguson,
  4. M R Davis,
  5. D T Graham,
  6. A R Pomeroy,
  7. D P Dhall

    Abstract

    The potencies of six commercially manufactured heparins have been measured by the British Pharmacopoeial (BP) assay and activated partial thromboplastin time (APTT), protamine sulphate, and anti-Xa assays. The APTT/BP potency ratios were found to vary with the preparation but this was not dependent on the tissue source of heparin. For mucosal heparins, the anti-Xa/BP potency ratios were close to unity, but for heparin of lung origin the anti-Xa potency was approximately one-quarter of the BP potency. Four heparin fractions prepared by column gel chromatography of a commercial heparin were similarly examined by all four assays, and there was a wide divergence between the BP potency estimates and those obtained with the other methods. The degree of divergence was found to depend on the molecular size of the fraction.

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