Development and characterization of an automated assay of effective heparin activity in plasma.
- 1 September 1987
- journal article
- research article
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 33 (9) , 1630-1634
- https://doi.org/10.1093/clinchem/33.9.1630
Abstract
We describe a fully automated assay for determining effective heparin activity in plasma, based on heparin-catalyzed inhibition of Factor Xa (EC 3.4.21.6) by antithrombin III (AT III). Residual Factor Xa is determined kinetically by the Du Pont aca discrete clinical analyzer with a chromogenic substrate and is inversely related to heparin activity. Because the test plasma is the sole source of AT III, the assay result is dependent on AT III activity and reflects effective rather than total heparin activity. The assay range is 20-1200 USP units/L, and the assay shows equivalent sensitivity to standard and low-molecular-mass heparins. Within-run reproducibility (CV) is 1.6% at 390 units/L. There was no interference from common blood components or drugs. Results agreed well with those by the Coatest heparin kit (Kabi) adapted to the Cobas-Bio analyzer (r = 0.85, n = 122).This publication has 7 references indexed in Scilit:
- Optimization of enzyme-based assays in coagulation testing.Clinical Chemistry, 1983
- Activation of factor X and prothrombin in antithrombin-III depleted plasma: The effects of heparinThrombosis Research, 1981
- Heparin Monitoring and ThrombosisAmerican Journal of Clinical Pathology, 1979
- Assay for plasma heparin using a synthetic peptide substrate for thrombin: Introduction of the fluorophore aminoisophthalic acid, dimethyl esterThrombosis Research, 1978
- The effect of metal ions on the amidolytic activity of human factor Xa (Activated Stuart-Prower Factor)Archives of Biochemistry and Biophysics, 1978
- Inactivation of bovine and human thrombin and factor Xa by antithrombin III studied with amidolytic methodsThrombosis Research, 1977
- Evaluation of an amidolytic heparin assay method: Increased sensitivity by adding purified antithrombin IIIThrombosis Research, 1977