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. 2013 Jan 10;14(1):294–300. doi: 10.1208/s12249-012-9915-z

Table V.

Pharmacokinetic Parameters of the In Vivo Study (n = 3)

Pharmacokinetic parameters Oral Transdermal
Cmax/μg·mL−1 0.2929 ± 0.1607 0.4964 ± 0.0763
Tmax/h 0.56 ± 0.19 1.67 ± 0.58
AUC0→t/μg·h·mL−1 0.5259 ± 0.2278 7.860 ± 2.151
F 1,494%

Cmax peak concentration, Tmax peak time, AUC bioavailability, F relative bioavailability of transdermal administration to oral