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. 2018 Oct 5;14(3):313–320. doi: 10.1016/j.ajps.2018.08.007

Table 5.

Pharmacokinetic parameters of dutasteride after oral administration of the reference (Avodart®) or DuγCD-PS complex at a dose of 2.39 mg/kg of dutasteride in rats.

Rx Tmax (h) Cmax (ng/ml) AUC0-24h (ng·h/ml) Relative BA% (to the reference)
Reference (Avodart®) 10.4 ± 7.8 253.4 ± 22.8 4336.9 ± 497.4
F1 12.0 ± 8.0 63.7 ± 23.5 1282.4 ± 334.9 29.6
F2 8.9 ± 9.0 148.8 ± 31.9 3147.3 ± 689.1 72.6
F3 10.4 ± 7.8 170.6 ± 43.4 3228.2 ± 459.9 74.4
F4 3.0 ± 1.2 215.2 ± 51.3 4061.1 ± 588.9 93.6
F5 11.0 ± 8.9 195.8 ± 21.3 4060.2 ± 295.3 93.6

Each value is the mean ± SD (n = 4–6).