D. Pape et al., NONINTERCHANGEABILITY OF SPECIFIC RADIOIMMUNOASSAY AND MONOCLONAL-ANTIBODY FLUORESCENT POLARIZATION IMMUNOASSAY IN CYCLOSPORINE MEASUREMENTS, Fundamental and clinical pharmacology, 10(5), 1996, pp. 484-489
This study compares cyclosporine (CsA) concentrations in whole blood f
rom patients receiving bone marrow (n = 10), renal (n = 48), heart (n
= 50) or liver (n = 50) transplants, as measured by monoclonal antibod
y flurorescence polarization immunoassay (FPIA) and specific I-125-rad
ioimmunoassay (RIA). The FPIA overestimated CsA by an average of 25%.
Results were higher for all indications: FPIA/RIA ratios were 1.17 for
bone marrow, 1.23 for renal and 1.27 for both heart and liver transpl
ants, and these values were significantly different from 1.0. The perc
entage of overestimation was higher at low CsA concentrations (less th
an or equal to 100 mu g/L) than at high CsA concentrations (greater th
an or equal to 400 mu g/L). In all indications, results by both method
s correlated well (r > 0.96) but slopes and intercepts were different
from 1.0 and 0.0, respectively, and these parameters varied greatly be
tween the grafted populations. These findings obtained with the two me
thods could nor be attributed to matrix effect because the mean FPIA/R
IA ratio for spiked control samples was 1.0. The discrepancy between t
he FPIA and RIA could be explained by the lower specificity of the mon
oclonal antibody contained in the FPIA kit. These results suggest that
FPIA is not as accurate as RIA and that the two methods are not inter
changeable in CsA level measurement.