PK parameter | Unit | Mean ± SD |
---|
A | μg/mL | 2.09 ± 1.46 |
B | μg/mL | 0.41 ± 0.17 |
α | 1/h | 0.81 ± 0.41 |
β | 1/h | 0.10 ± 0.02 |
Ka | 1/h | 2.00 ± 0.51 |
K10 | 1/h | 0.25 ± 0.08 |
K12 | 1/h | 0.32 ± 0.20 |
K21 | 1/h | 0.34 ± 0.23 |
T1/2Ka | h | 0.37 ± 0.09 |
T1/2α | h | 1.07 ± 0.60 |
T1/2β | h | 7.28 ± 1.10 |
AUC | h*μg/mL | 5.25 ± 1.35 |
Tmax | h | 0.97 ± 0.08 |
Cmax | μg/mL | 0.76 ± 0.08 |
CL | L/h | 7.75 ± 1.74 |
Vc | liter/kg | 2.28 ± 0.39 |
Vp | liter/kg | 2.16 ± 0.86 |
Vss | liter/kg | 4.17 ± 0.76 |
- A and B: Y-axis intercept terms; α: distribution rate constant; β: elimination rate constant; Ka: absorption rate constant; K10: central compartment elimination rate constant; K12: rate constant from central to peripheral compartment; K21: rate constant from peripheral to central compartment; T1/2Ka: absorption half-life of the drug; T1/2α: distribution half-life of the drug; T1/2β: elimination half-life of the drug; AUC: area under the curve of plasma concentration-time; Tmax: the time point of maximum plasma concentration of the drug; Cmax: the maximum plasma concentration; CL: body clearance; Vc: volume of distribution in the central compartment; Vp: volume of distribution; Vss: volume of distribution at steady state