Pharmacokinetic and Bioavailability Studies of Embelin after Intravenous and Oral Administration to Rats

Table 3

Main pharmacokinetic parameters of embelin (n=6, mean±SD).

Parameters	intravenous (5mg/kg)	oral administration (15mg/kg)
(h)	0.03±0.00	0.71±0.19
(μg/mL)	3.91±1.34	1.05±0.21
(μg/mL h)	2.17±0.49	1.97±0.78
(μg/mL h)	3.21±0.62	2.92±0.69
t1/2(h)	1.52±0.83	1.01±0.58
(h)	1.28±0.11	1.49±0.49
(h)	3.43±0.41	3.21±1.15