Thromb Haemost 1989; 61(02): 289-293
DOI: 10.1055/s-0038-1646578
Original Article
Schattauer GmbH Stuttgart

Evaluation of Fibrinolytic Capacity in Plasma during Thrombolytic Therapy with Single (scu-PA) or Two-chain Urokinase Type Plasminogen Activator (tcu-PA) by a Combined Assay System for Urokinase Type Plasminogen Activator Antigen and Function

Johann Wojta
1   The Department of Pathology and Pediatrics, Vanderbilt University, Nashville, TN, USA
2   The Laboratory for Clinical Experimental Physiology, Department of Medical Physiology, Universityof Vienna, Austria
,
Bernd R Binder
2   The Laboratory for Clinical Experimental Physiology, Department of Medical Physiology, Universityof Vienna, Austria
,
Kurt Huber
3   The Department of Cardiology, University of Vienna, Austria
,
Richard L Hoover
1   The Department of Pathology and Pediatrics, Vanderbilt University, Nashville, TN, USA
› Author Affiliations
Further Information

Publication History

Received 23 February 1988

Accepted after revision 08 November 1988

Publication Date:
30 June 2018 (online)

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Summary

A combined assay for urokinase type plasminogen activator (u-PA) activity and antigen determination in plasma samples is described. This assay is based on binding of u-PA to an antibody immobilized on a microtiter plate followed by determination of the enzymatic activity of the bound u-PA. Thereafter bound u-PA antigen can be quantified by means of a specific peroxidase labelled monoclonal antibody against u-PA. By use of this assay system u-PA activity and antigen can be determined with lower detection limits of 0.08 IU/ml and 1.0 ng/ml, respectively, and intraassay as well as interassay coefficients of variation of 10% and 12% for activity and 5% and 7% for antigen determinations, respectively. Normal plasma levels of u-PA antigen could be determined to be 1.88 nglml ± 0.61. Furthennore, this assay system allows specific quantification of u-PA antigen and activity during thrombolytic therapy.