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. 2000 Jun;44(6):1598–1603. doi: 10.1128/aac.44.6.1598-1603.2000

TABLE 2.

Effects of early or delayed treatment with AMB-DOC or its derivates on survival of leukopenic micea and growth of C. albicans in the kidney

Time of treatment Drug usedb Dose (mg of AMB/kg) Log10 CFU/kidneyc at time of treatment Day 7 after inoculation
Survival rate (%) Log10 CFU/kidneyc in surviving mice No. of mice with sterile kidneys/no. of surviving mice
6 h None (untreated) 3.3 ± 0.2
Placebo (5-DW) 0
AMB-DOC 0.8 100 5.1 ± 0.6 0/10
hAMB-DOC 0.8 100 5.0 ± 0.6 0/10
hAMB-DOC 3 100 1.0 ± 0.8d 3/10
hcAMB-DOC 0.8 100 5.2 ± 0.6 0/10
hcAMB-DOC 3 100 1.3 ± 0.5d 0/10
16 h None (untreated) 4.2 ± 0.1
Placebo (5-DW) 0
AMB-DOC 0.1 0
hAMB-DOC 0.6 100 5.1 ± 0.7 0/10
hcAMB-DOC 0.6 60 5.8 ± 0.8 0/6
a

Leukopenic mice were inoculated i.v. at time zero with 3 × 104 CFU of C. albicans; untreated mice died within 3 days after C. albicans inoculation. 

b

AMB-DOC, its derivates, and placebo were administered i.v. 

c

Each value is the geometric mean ± SD. 

d

Significant decrease (P ≤ 0.001) from number of CFU at the time of treatment.