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. 2016 Aug 1;233:3371–3381. doi: 10.1007/s00213-016-4379-6

Table 3.

Pharmacokinetic model estimates for group 1 and the combined (groups 1 and 2) sample

Parameter (units) Group 1 (n = 20) Combined (n = 45)
Estimate RSE (%) Estimate RSE (%)
ka 0.87 14 0.85 16
Cl 84 7 54.3 8
β-Cl,weight 0.75 ne 0.75 ne
β-Cl,Age ne ne −2.9 (p = 2.3e-007)
V1 668 (Men) 15 455 13
399 (Women) 13
β-V1, weight 1 ne ne ne
β-V1,Gender −0.52 (p = 6.6e-005) 25 ne ne
Q 117 15 111 16
β-Q,weight 0.75 ne ne ne
V2 population 808 12 736 11
β-V2,weight 1 ne ne ne
Random effect
ω_ka% 37 21 48 24
ω_Cl% 31 16 36 16
ω_V1% 42 21 43 27
ω_Q% 61 19 63 20
ω_V2% 50 17 46 18
ω_Cl_V1% 73 19 73 23
ω_Cl_Q% 68 21 60 29
ω_V1_Q% 51 48 73 23
ω_Cl_V2% 60 25 66 22
ω_V1_V2% 97 9 90 16
ω_Q_V2% 54 33 60 30
Residual error
σ (group 1)% 13 5 13 6
σ (group 2)% 53 24

ka absorption constant, Cl apparent clearance from central compartment, V1 central volume of distribution, Q intercompartmental clearance, V2 peripheral volume of distribution, ω inter-individual variability (expressed as a percentage), σ residual unexplained variability (expressed as a percentage and separated on the basis of group), weight log transformed and centred around a standard 70 kg weight, age log transformed and centred around the mean, RSE relative standard error, ne not estimated