Skip to main content
. Author manuscript; available in PMC: 2014 Jul 31.
Published in final edited form as: Pharmacogenomics. 2013 Jul;14(10):1141–1151. doi: 10.2217/pgs.13.94

Table 5.

Population pharmacokinetics analysis.

Parameters Weight-based model, estimate (%CV) Final model with OCT-dependent CL, estimate (%CV) Bootstrap value, median (%CV)
Fixed effects
CL (l/min) 1.2 (9.7) 1.2 (9.9) 1.2 (10.5)
Factor for OCT1 homozygotes 0.83 (6.2) 0.83 (6.4)
V1 (l) 3.9 (38.9) 3.9 (38.5) 4.0 (36)
Q (l/min) 1.6 (32.3) 1.6 (32.1) 1.6 (30.2)
V2 (l) 21.3 (22.3) 21.2 (22.3) 20.9 (21.9)
γ CL 0.75 0.75 0.75
γ V1 1 1 1
γ Q 0.75 0.75 0.75
γ V2 1 1 1
Interindividual variability
Omega on CL 0.1826 (13.2) 0.173 (14.3) 0.172 (29.9)
Residual error
Proportional 0.2464 (9.7) 0.2478 (9.7) 0.245 (19.3)

All reported pharmacokinetic parameters are for a standard adult weighing 70 kg.

γCL: Allometric coefficient for clearance; γQ; Allometric coefficient for intercompartmental clearance; γv1: Allometric coefficient for central volume; γV2: Allometric coefficient for peripheral volume; CL: Clearance; CV: Coefficient of variation; Q: Intercompartmental clearance; V1: Central volume; V2: Peripheral volume.