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. 2024 Apr 25;11:1389810. doi: 10.3389/fvets.2024.1389810

Table 1.

PK parameters (mean ± SEM) of CBD following single oral dose administration of one of four different dosage forms.

Pharmacokinetic parameter OM (n = 7) NM (n = 6) WM (n = 6) CM (n = 6) p-value
AUC0-t (μg/L*h) 1432.06 ± 208.38 853.29 ± 188.83 1158.98 ± 317.83 296.05 ± 41.22 0.0431 a
AUC0-inf (μg/L*h) 1494.14 ± 209.87 935.19 ± 200.42 1308.98 ± 378.85 313.84 ± 41.92 0.0381 a
Cmax (μg/L) 270.10 ± 31.88 175.35 ± 28.19 314.30 ± 81.09 92.29 ± 21.45 0.1329 a
Tmax (h) 3.21 ± 0.82 2.00 ± 0.37 2.58 ± 0.80 2.83 ± 0.70 0.6584
T1/2 (h) 8.47 ± 1.31 10.19 ± 1.35 10.23 ± 4.05 9.56 ± 1.01 0.4796
Ke (1/h) 0.10 ± 0.02 0.08 ± 0.01 0.11 ± 0.03 0.08 ± 0.01 0.4467
Vz/F (L/kg) 55.94 ± 19.80 93.93 ± 15.01 64.48 ± 12.88 141.75 ± 20.30 0.0199
CL/F (L/h/kg) 4.00 ± 0.85 7.00 ± 1.80 5.59 ± 1.31 10.54 ± 1.61 0.0381
MRTinf (h) 8.96 ± 0.27 9.77 ± 1.11 10.69 ± 3.66 8.14 ± 0.75 0.5032
a

A value of p ≤ 0.05 was defined as significant and indicated the data with dose-normalization where applicable.

CBD infused in an oil base (OM), a nanoemulsion base (NM), a water-soluble base (WM), or a semi-solid form (CM) in the OM, NM, WM and CM groups, respectively, where p values are based on post hoc multiple comparisons using Brown-Forsythe ANOVA and otherwise (underlined) using non-parametric Kruskal-Wallis test.