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. 2013 Oct 9;9:202. doi: 10.1186/1746-6148-9-202

Table 1.

Pharmacokinetic parameters of phenobarbital following oral administration of 100 mg Luminal® vet or Phenoleptil® in a group of 8 dogs

Parameter Luminal® vet Phenoleptil® P
Tmax (h) observed
3.75 ± 0.79
2.75 ± 0.37
0.2275
Tmax (h) calculated
5.97 ± 1.33
2.64 ± 0.51
0.0588
Cmax (μg/ml) observed
10.9 ± 0.92
10.5 ± 0.77
0.2426
Cmax (μg/ml) calculated
10.3 ± 0.92
10.0 ± 0.85
0.2569
T0.5 (h)
50.3 ± 3.1
52.9 ± 2.8
0.2348
AUC(0-119) (μg ml-1 h) observed
644 ± 52.5
618 ± 44.5
0.1499
AUC∞ (μg ml-1 h) calculated
807 ± 66.8
781 ± 54.0
0.2961
Relative bioavailability (AUCPhenoleptil® /AUCLuminal® vet)
0.98 ± 0.031
(range: 0.90-1.15; 90% CI: 0.92-1.04)
Relative Cmax observed (Cmax, observed Phenoleptil®/ Cmax, observed Luminal® vet)
0.96 ± 0.031
(range: 0.85-1.05; 90% CI: 0.90-1.03)
Relative Cmax calculated (Cmax, calculated, Phenoleptil®)/Cmax, calculated, Luminal® vet)
0.97 ± 0.028
  (range: 0.81-1.08; 90% CI: 0.92-1.03)

All data are shown as means ± SEM; for ratios also the range and 90% confidence intervals (90% CI) are shown. Abbreviations: Tmax, time to reach peak plasma concentration; Cmax, peak plasma concentration; t0.5, elimination half-life in plasma; AUC, area under the plasma concentration curve.