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. 2013 Mar 7;18(3):3050–3059. doi: 10.3390/molecules18033050

Table 5.

Main pharmacokinetic parameters of QGR in rats determined after intravenous and oral administration (n = 3, mean ± SD).

PK parameters Unit Intravenous Oral
t1/2 min 118.89 ± 5.65 236.87 ± 28.59
AUC(0t) μg/mL × min 1,775.96 ± 36.92 120.81 ± 11.38
AUC(0∞) μg/mL × min 1,790.24 ± 37.53 122.14 ± 16.15
Tmax min - 20
Cmax ng/mL - 495.69 ± 58.36
F % - 3.41 ± 1.21