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. 2017 Oct;363(1):12–19. doi: 10.1124/jpet.117.243246

TABLE 1.

Pharmacokinetic parameters of ponatinib in WT mice and hCYP1A1/2 pre-treated with TCDD or 3-MC

The PK parameters were calculated as outlined in Materials and Methods. The P values were calculated using an unpaired t test: *P ≤ 0.05; **P ≤ 0.01; ***P ≤ 0.001.

Genotype
Pretreatment
t1/2
Cmax
AUC0–8 hours
AUC0–∞
hour µg/ml hour*µg/ml hour*µg/ml
WT Vehicle 6.2 ± 0.2 1,212 ± 222 7,011 ± 1,490 12,620 ± 2,230
WT TCDD 2.4 ± 0.8** 253 ± 42** 908 ± 59** 1,044 ± 175**
hCYP1A1/1A2 Vehicle 13.9 ± 1.7 705 ± 96 4,170 ± 500 9,740 ± 2,100
hCYP1A1/1A2 3-MC 4.6 ± 0.8** 620 ± 245 1,920 ± 520* 3,650 ± 1,890*