TABLE 1.
Total dose (mg/kg/day) | Regimen (mg/kg) | Day 4
|
Day 7
|
||
---|---|---|---|---|---|
No. of infected animals/total (%) | Log CFU/swab (mean ± SD) | No. of infected animals/total (%) | Log CFU/swab (mean ± SD) | ||
None | 13/13 (100) | 4.0 ± 0.7 | 13/13 (100) | 3.9 ± 0.6 | |
3.75 | 1.25 TID | 5/5 (100) | 3.6 ± 0.9 | 4/5 (80) | 2.7 ± 0.8 |
5 | 5 OD | 5/5 (100) | 3.7 ± 0.8 | 4/5 (80) | 2.4 ± 0.4∗ |
7.5 | 2.5 TID | 5/5 (100) | 2.8 ± 0.3∗ | 3/5 (60) | 2.5 ± 0.3∗ |
10 | 5 BID | 5/5 (100) | 3.3 ± 0.5∗ | 3/5 (60) | 2.6 ± 0.4∗ |
15 | 5 TID | 2/5 (40) | 2.7 ± 0.3∗ | 0/5 (0) | <1.6∗∗ |
30 | 10 TID | 0/5 (0) | <1.6∗∗ | 0/5 (0) | <1.6∗∗ |
Rats were orally infected three times at 24-h intervals with 3 × 108 C. albicans 4711E cells/ml. GM237354 was administered subcutaneously once a day (OD), twice a day (BID), or TID for seven consecutive days (day 0 to day 6). The mean log CFU/swab just before treatment was 5.0 ± 0.7 (n = 43). ∗, P < 0.05; ∗∗, P < 0.01 (versus the control treatment). The limit of detection was 40 CFU/swab.