TABLE 1.
Parameter | Estimate | % SE |
---|---|---|
CL (liters/h) | 1.18 | |
V (liters) | 41 | |
ka (h−1) | 2 | |
MTT (h) | 1.1 | |
No. of transit compartments | 10 | |
θdose,F | 0.025 | |
CLm/Fm (liters · h−1) | 3.1 | 22.3 |
Vm/Fm (liters) | 15.5 | 18.3 |
θdose,Fm | 0.049 | 57.6 |
IIVa (variances plus % CV) | ||
ƞCL | 0.136 (36.9) | |
ƞV | 0.0566 (23.8) | |
ƞMTT | 0.307 (55.4) | |
ƞCLm | 0.32 (56.6) | 32.2 |
Covariance for ƞCL∼ ƞV (covariance and correlation) | 0.0684 (0.780) | |
Residual variability | ||
Additive error for RFP (mg · liter−1) | 0.48 | 14.4 |
Proportional error for RFP | 0.26 | 3.0 |
Additive error for desRFP (mg · liter−1) | 0.072 | 17.8 |
Proportional error for desRFP | 0.40 | 2.5 |
IIV, interindividual variability. Values of IIV are shown in parentheses as % CV; etas represent the random variable with zero mean that distinguishes individual pharmacokinetic parameters from the population mean (the variances of etas are data before the parentheses).