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. 2020 Sep 23;2:100056. doi: 10.1016/j.ijpx.2020.100056

Table 3.

Pharmacokinetic profiles of after GemHCl and 4NSG were administered intravenously to mice.

Parameter Unit One-compartment model
Significance level p-value
GemHCl 4NSG
K10 1/h 1.01 ± 0.03 0.36 ± 0.04 0.0001
t1/2 h 0.70 ± 0.01 1.93 ± 0.06 0.0001
Vd mL 21.7 ± 1.9 19.3 ± 0.2 0.3619
CL mL/h 21.3 ± 3.2 7.1 ± 1.1 0.0001
AUC (0-t) μg/(mL * h) 28.2 ± 4.3 86.2 ± 5.4 0.0001
AUMC(0-inf) μg/(mL * h2) 28.2 ± 4.1 86.6 ± 4.8 0.0001
MRT h 1.2 ± 0.1 2.8 ± 0.4 0.02
Vss μg/(μg/mL) 21.7 ± 3.6 23.9 ± 1.6 ns

k10, elimination rate constant; t1/2, half-life; AUC(0-t),area under the plasma concentration–time curve; AUMC(0-inf), area under the first moment curve; MRT, mean residence time; Cl, clearance; Vd, volume of distribution; Vss, volume of distribution at steady state. (Data analyzed using t-test).