Standardization of methods for measuring plasminogen activator inhibitor activity in human plasma

Clin Chem. 1989 May;35(5):787-93.

Abstract

We have standardized the measurement of plasminogen activator inhibitor type 1 (PAI-1) activity in plasma. One-chain tissue-type plasminogen activator (t-PA; EC 3.4.21.31; final activity, 5 int. units/mL) was incubated with plasma (final dilutions 1:4 to 1:40) in phosphate buffer (pH 7.4, ionic strength = 0.15) for 15 min at 37 degrees C, followed by acidification and measurement of residual t-PA activity by an amidolytic method. The PAI-1 activity assay was 98% specific for PAI-1 activity in samples from both pregnancy and nonpregnancy, and varied linearly with added plasma volume when the percent inhibition of t-PA was between 8% and 50%. For the standardized method, analytical recovery was 93 +/- 5%, the detection limit was 1.6 arbitrary units per milliliter (1 arb. unit of PAI-1 activity = inhibition of 1 int. unit of t-PA activity), and total imprecision was 10.2 (SD 0.7) arb. units/mL (CV = 7%, n = 20). The average PAI-1 activity in 10 healthy individuals drawn between 0800 and 1000 hours was 23.9 +/- 15.4 arb. units/mL. Compared with the standardized assay, two of three previously described assays underestimated PAI-1 activity in plasma by 77% and 85%, respectively.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Blood Chemical Analysis / standards
  • Buffers
  • Chromogenic Compounds
  • Cyanogen Bromide
  • Female
  • Glycoproteins / blood*
  • Glycoproteins / immunology
  • Humans
  • Hydrolysis
  • Peptide Fragments / blood
  • Plasminogen Activators / antagonists & inhibitors*
  • Plasminogen Inactivators*
  • Pregnancy

Substances

  • Buffers
  • Chromogenic Compounds
  • Glycoproteins
  • Peptide Fragments
  • Plasminogen Inactivators
  • Plasminogen Activators
  • Cyanogen Bromide