Table 1.
Toxicokinetic parameters (unit) | Value |
---|---|
Intravenous administration | |
Kel (h) | 0.53 ± 0.11 |
K12 (h−1) | 1.33 ± 0.10 |
K21 (h−1) | 0.68 ± 0.17 |
t1/2α (h) | 0.10 ± 0.01 |
t1/2β (h) | 1.36 ± 0.29 |
CL (L/h/kg) | 0.34 ± 0.03 |
Vd (L/kg) | 6.40 ± 0.89 |
MRT (h) | 2.1 ± 0.41 |
Oral administration | |
Cmax (ng/ml) | 15.9 ± 4.5 |
Tmax (min) | 15.0 ± 0.0 |
Fpo (%) | 29.66 ± 5.6 |
Kel, elimination rate constant; K12, K21, micro-rate constants; t1/2α, distribution half-life; t1/2β, elimination half-life; CL, clearance; Vd, volume of distribution; MRT, mean residence time; Cmax, maximum concentration; Tmax, time at maximum concentration; Fpo, oral bioavailability.