TY - JOUR
T1 - Standardization of methods for measuring plasminogen activator inhibitor activity in human plasma
AU - Chandler, W. L.
AU - Loo, S. C.
AU - Nguyen, S. V.
AU - Schmer, G.
AU - Stratton, J. R.
PY - 1989
Y1 - 1989
N2 - 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°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 in. 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 wtih the standardized assay, two of three previously described assays underestimated PAI-1 activity in plasma by 77% and 85%, respectively.
AB - 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°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 in. 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 wtih the standardized assay, two of three previously described assays underestimated PAI-1 activity in plasma by 77% and 85%, respectively.
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U2 - 10.1093/clinchem/35.5.787
DO - 10.1093/clinchem/35.5.787
M3 - Article
C2 - 2498016
AN - SCOPUS:0024400739
SN - 0009-9147
VL - 35
SP - 787
EP - 793
JO - Clinical Chemistry
JF - Clinical Chemistry
IS - 5
ER -