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Average resveratrol pharmacokinetic parameters in both rats and human.
| Bioavailability | Volume of distribution | Systemic clearance | Elimination half-life | ||||
|---|---|---|---|---|---|---|---|
| F (%) | V d (L/kg) | Cl (mL/min/kg) | t 1/2 (min) | ||||
| Rats | Human | Rats | Human | Rats | Human | Rats | Human |
| 29 | 70 | 35 | 30 | 184 | 157 | 130 | 180 |
