Table 1.
Pharmacokinetic parameters for three models
In vivo | PBPK | PBPK-LiverODE | PBPK-GSMN | ||
---|---|---|---|---|---|
i.v. – 0.3 mg | AUC | 10.2 ± 1.18 | 10.4 ± 0.23 | 6.1 ± 0.17 | 5.9 ± 0.56 |
Oral – 2 mg | Tmax | 3.8 ± 0.4 | 2.5 ± 0.34 | 3.5 ± 0.38 | 2.4 ± 0.18 |
Cmax | 0.44 ± 0.24 | 0.34 ± 0.19 | 0.35 ± 0.24 | 0.32 ± 0.23 | |
AUC | 10.3 ± 1.18 | 8.9 ± 0.19 | 9.2 ± 0.13 | 8.1 ± 0.04 | |
Oral – 4 mg | Tmax | 3.4 ± 0.6 | 3.1 ± 0.31 | 3.2 ± 0.35 | 2.3 ± 0.26 |
Cmax | 0.63 ± 0.3 | 0.67 ± 0.25 | 0.71 ± 0.26 | 0.65 ± 0.21 | |
AUC | 13.4 ± 3.47 | 17.3 ± 0.38 | 17.4 ± 0.24 | 16.2 ± 0.09 |