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. 2014 Jan;85(1):139–147. doi: 10.1124/mol.113.088914

TABLE 1.

Pharmacokinetic parameters for plasma LVA in LCN and WT mice

Data from Fig. 3 were used for the determination of pharmacokinetic parameters, as described in Materials and Methods. Values represent means ± S.D. (n = 5 to 6).

Strain Dose Tmax Cmax t1/2 AUC0–4h CL/F
mg/kg min μg/ml min min ⋅µg/ml ml/min
WT 50 27.4 ± 7.8 0.67 ± 0.11 49.6 ± 10.0 56.5 ± 8.9 18.1 ± 3.0
LCN 33.8 ± 10.6 1.30 ± 0.19* 68.2 ± 14.7** 154.5 ± 30.6* 6.7 ± 1.4*
WT 5 15.0 ± 0 0.067 ± 0.008 27.4 ± 12.2 4.1 ± 1.1 29.1 ± 9.2
LCN 20.0 ± 8.7 0.033 ± 0.004** 26.7 ± 12.8 2.1 ± 0.4** 49.4 ± 10.2

AUC, area under the curve.

*

P < 0.01; **P < 0.05; compared with the corresponding WT group (Student’s t test).