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. 2023 Oct 4;14:1263975. doi: 10.3389/fphar.2023.1263975

TABLE 6.

Pharmacokinetic parameters of rivaroxaban in rats after oral administration alone and combined multiple doses of almonertinib.

Parameters (Unit) Rivaroxaban (2 mg/kg, group 1) Multiple-doses almonertinib with rivaroxaban (2 mg/kg, group 5) Multiple-doses almonertinib with rivaroxaban (1 mg/kg, group 6)
AUC0-t (μg/L*h) 763.89 ± 164.17 3,511.15 ± 783.84** 2,216.88 ± 455.02**
AUC0-∞(μg/L*h) 796.70 ± 168.72 3,536.15 ± 793.55** 2,234.87 ± 464.38**
Cmax (μg/L) 200.50 ± 37.99 862.00 ± 110.34** 457.33 ± 101.03**
Tmax (h) 0.92 ± 0.30 2.21 ± 0.95** 2.08 ± 0.49**
t1/2z (h) 6.84 ± 3.46 4.47 ± 0.80 4.30 ± 0.91
CLz/F (L/h/kg) 2.62 ± 0.62 0.60 ± 0.18** 0.47 ± 0.12**
Vz/F (L/kg) 26.35 ± 18.02 3.75 ± 0.72** 2.83 ± 0.55**
MRT0-t (h) 4.72 ± 0.57 3.94 ± 0.56* 4.10 ± 0.41
MRT0-∞ (h) 6.09 ± 1.45 4.12 ± 0.60** 4.30 ± 0.47**

*p < 0.05, **p < 0.01, compared with 2 mg/kg rivaroxaban alone, demonstrating statistically significant difference. The main pharmacokinetic parameters are revealed as the mean ± standard deviation.