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. Author manuscript; available in PMC: 2015 May 20.
Published in final edited form as: Drug Test Anal. 2009 Jan;1(1):14–21. doi: 10.1002/dta.12

Table 1.

Pharmacokinetic parameters of IFLs

Cmaxa rb tmaxc t1/2d C24e C36f C48g
(μM) (hours) (hours) (rel. to Cmax) (%) (rel. to Cmax) (%) (rel. to Cmax) (%)
DE 1.97 ± 0.63 0.93 6.2 ± 1.5 7.7 ± 3.3 20 7 2
GE 2.37 ± 0.41 0.71 5.7 ± 1.8 9.5 ± 3.2 26 11 5
D* 3.46 ± 0.75 0.85 7.5 ± 1.6 7.0 ± 1.6 20 6 2
G* 3.78 ± 1.00 0.85 6.8 ± 1.4 9.5 ± 1.7 29 12 5
a

Peak plasma levels in μM per mg IFL per kg BW.

b

correlation between dose and plasma levels by linear regression.

c

time to reach peak plasma levels.

d

time to reach peak plasma levels.

a–d

mean of 16 studies.[59]

e

% plasma level after 24 hours relative to peak plasma levels.

f

% plasma level after 36 hours relative to peak plasma levels.

g

% plasma level after 48 hours relative to peak plasma levels.

*

When dosed in aglycon units.