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. 2019 May 2;10:459. doi: 10.3389/fphar.2019.00459

Table 4.

Comparison of pharmacokinetic parameters of TAL after oral administration of TAL powder and SNEDDS formulation [F6, I308: TC (1:1)/HCO-30 (1/1)] containing TAL.

Parameter Unit TAL Powder ± SEM TAL SNEDDS ± SEM % Control
Lambda_z 1/h 0.39 0.03 0.41 0.03 6.11
t1/2 h 1.81 0.17 1.70 0.18 6.00
Tmax h 1.50 0.00 1.50 0.00 0.00
Cmax ng/ml 340.75*** 27.80 593.05*** 36.99 74.04
AUC 0-t ng/mlh 927.35*** 56.02 1468.23*** 78.29 58.33
AUC 0-t/0-inf_obs 0.94 0.01 0.96 0.01 1.55
MRT 0-inf_obs H 3.16 0.34 3.06 0.67 3.10
Vz/F_obs (mg)/(ng/ml) 0.37** 0.84 0.02** 0.001 95.70
Cl/F_obs (mg)/(ng/ml)/h 0.15* 0.39 0.01* 0.0001 95.594

Data are expressed as mean ± SEM (n = 6), p < 0.05, ∗∗p < 0.001, and ∗∗∗p < 0.0001. Tmax, time of peak concentration; Cmax, peak of maximum concentration; AUC0t, area under the concentration time profile curve up to time 24 h; AUC0→∞, area under the concentration time profile curve extrapolated to infinity; Kel, elimination rate constant; Vss, volume of distribution at steady state; T1/2, half-life; MRT, mean residence time; CL/F, oral clearance.