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. 2022 Nov 23;27(23):8140. doi: 10.3390/molecules27238140

Table 2.

Pharmacokinetic parameters of M10 in DSS-group mice tissues after oral administration of M10 at a dose of 50 mg/kg (mean ± SD, n = 3).

Parameters Colon Small Intestine Stomach Liver Spleen Lung Kidney
Cmax (ng/mL) 5742.32 ± 3986.73 8332.84 ± 3882.24 156,014.34 ± 74,478.59 417.13 ± 91.93 242.35 ± 34.51 133.65 ± 41.13 5607.33 ± 1791.25
Tmax (h) 2.03 ± 1.96 0.08 ± 0.00 0.08 ± 0 2.25 ± 3.25 2.67 ± 1.56 0.5 ± 0.43 2.06 ± 3.42
T1/2 (h) 0.52 ± 0.53 7.20 ± 7.34 2.06 ± 0.70 28.14 ± 0 7.15 ± 2.17 1.13 ± 0.80 * 2.75 ± 2.05
MRT (h) 0.524 ± 0.53 * 1.45 ± 0.35 1.26 ± 0.25 4.20 ± 0.45 3.97 ± 0.20 1.88 ± 0.70 3.73 ± 1.73
AUC0–t (ug/L * h) 6694.89 ± 7279.721 4248.33 ± 1659.42 79,911.87 ± 14,176.32 1099.64 ± 212.87 1470.70 ± 194.90 210.52 ± 35.58 5066.59 ± 3652.48
AUC0–∞ (ug/L * h) 6809.75 ± 7478.41 4989.31 ± 1007.26 83,897.97 ± 16,033.17 2163.86 ± 1645.71 2957.86 ± 594.32 233.66 ± 48.96 10,496.80 ± 11,408.11

* p < 0.05 for DSS-group mice compared with normal-group mice.