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. 2021 Oct 5;22(19):10773. doi: 10.3390/ijms221910773

Table 8.

Mean values of pharmacokinetic parameters calculated from the concentrations of 2 and 3 compounds in serum and tissues after single i.p. administration at a dose of 0.3 mg/kg (non-compartmental analysis) (n = 4/time point).

2
Tissue Tmax
(min)
Cmax
(ng/mL or ng/g)
AUC0-t
(ng·min/mL or ng·min/g)
Kp
Serum 15 5.20 ± 2.24 453.40 ± 145.83 -
Brain 5 11.63 ± 3.13 1219.94 ± 368.79 2.69
Heart 5 8.90 ± 8.15 1040.74 ± 448.65 2.30
Lungs 5 54.20 ± 21.61 3870.66 ± 680.07 8.54
Liver * 15 115.22 ± 93.46 6523.60 ± 4997.28 14.39
Kidneys 15 65.73 ± 34.94 7488.06 ± 4372.92 16.52
3
Serum 5 6.32 ± 5.04 423.91 ± 216.75 -
Brain 5 11.35 ± 6.93 859.08 ± 312.87 2.03
Heart 5 21.83 ± 17.16 1057.37 ± 285.41 2.49
Lungs 5 73.65 ± 63.94 2715.09 ± 1000.42 6.41
Liver * 5 129.62 ± 106.23 ** 4467.18 ± 2249.99 10.54
Kidneys 15 41.25 ± 8.41 2557.08 ± 1084.42 6.03

Cmax—maximum concentration; Tmax—time to reach the maximum concentration; Kp—ratio of AUC0-t tissue to AUC0-t serum. * Cmax ratio (2/3) = 0.89. ** Expressed with molar concentration: Cmax = 0.395 µM.