Table 1.
Human (mg kg −1) |
Route | Intensity | Mouse (mg kg −1) |
Hamster (mg kg −1) |
---|---|---|---|---|
3–5 | Intravenous | Twice weekly | 37–62 | 22–37 |
10–15 | Intravenous | Every 7–10 days | 123–185 | 74–111 |
40–50a | Intravenous | Over 2–5 days | 492–615 | 296–370 |
1–5a | Oral | Daily | 12–62 | 7–37 |
Human equivalent schedules used in this murine study. To convert human doses expressed in mg kg−1 to animal doses, the human dose was multiplied by a factor of 12.3 for mouse and 7.4 for hamster. Clinical dose schedules were obtained from the Thomson Reuters (Healthcare) (Greenwood Village, CO, USA) DRUGDEX database.19 Human-to-animal conversion factors are based on recommendation by the US Food and Drug Administration for estimating the maximum safe starting dose in clinical trials.20 Mice were dosed intraperitoneally at 120 mg kg−1 daily for 4 days (human 10 mg kg−1 × 4 doses) or by oral gavage at 40 mg kg−1 daily for 8 days (human 3 mg kg−1 × 8).