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. 2021 Aug 19;59(1):1131–1136. doi: 10.1080/13880209.2021.1964544

Table 3.

The main pharmacokinetic parameters of ambrisentan in rat plasma in two groups (n = 6).

Parameters Group A Group B
AUC(0–t) (μg/L·h) 41,308.92 ± 19,275.09 53,368.89 ± 7,683.32*
AUC(0–∞) (μg/L·h) 44,893.16 ± 22,304.94 53,861.05 ± 7,773.54*
t1/2z (h) 0.92 ± 0.42 0.55 ± 0.11
Tmax (h) 0.60 ± 0.55 0.22 ± 0.08
Vz/F (L/kg) 0.09 ± 0.06 0.04 ± 0.01
CLz/F (L/h/kg) 0.07 ± 0.03 0.05 ± 0.01
Cmax (μg/L) 31,474.53 ± 18,255.05 57,182.51 ± 14,900.22*

Group A: control group; Group B: a single dose of 20 mg/kg shikonin. *p < 0.05.