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. 2018 Sep 5;9(11):1383–1389. doi: 10.1111/1759-7714.12843

Table 3.

Primary pharmacokinetic parameters after oral administration of AZD‐3759 in rats (n = 6, Mean ± SD)

Pharmacokinetics parameters Oral administration (n = 6)
AUC(0–t) (ng/mL·h) 4301.756 ± 890.667
AUC(0–∞) (ng/mL·h) 4403.952 ± 904.901
MRT(0–t) (h) 9.178 ± 0.932
MRT(0–∞) (h) 9.649 ± 1.358
t1/2 (h) 3.481 ± 0.91
Tmax (h) 9 ± 1.897
CL (L/h/kg) 2.339 ± 0.403
Vz (L/kg) 11.781 ± 3.872
Cmax (ng/mL) 325.983 ± 63.936

AUC, area under the plasma concentration–time curve; CL, plasma clearance; Cmax, maximum plasma concentration; MRT, mean residence time; SD, standard deviation; t1/2, half‐life; Tmax, maximum plasma time.