Table 21.

Pharmacokinetic parameters of HEDT-Glu Following after intravenous administration 13.2 mg·kg⁻¹ HEDT-Glu in rats (n = 6).

Parameters	Values
AUC	16.04 ± 3.19 μ g·h·mL−1.
Elimination half-life at the α phases (t1/2,a)	0.06 ± 0.01 h
Elimination half-life at the β phase (t1/2,b) phases	1.27 ± 0.31 h
Ke	9.78 ± 1.61 h−1
CL	0.85 ± 0.17 l·kg−1·h−1.

AUC = area under the concentration-time curve; CL = clearance; Ke = elimination rate constant.