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. 2001 Feb;45(2):596–600. doi: 10.1128/AAC.45.2.596-600.2001

TABLE 1.

Estimated compartmental pharmacokinetic parameters of caspofungin in plasmaa

Drug dose (mg/kg) Cmax (μg/ml) Cmin (24 h) (μg/ml) AUC0–∞ (μg/ml · h) Vss (liter/kg) CL (liter/h/kg) t1/2αb (h) t1/2β (h) t1/2γ (h)
Single dose
 1 20.02 ± 1.18 0.00 ± 0.00 20.57 ± 0.89 0.239 ± 0.011 0.050 ± 0.002 0.09 ± 0.00 2.00 ± 0.06 31.61 ± 0.12
 3 60.47 ± 8.49 0.00 ± 0.00 47.14 ± 3.60 0.277 ± 0.033 0.068 ± 0.005 0.05 ± 0.00 1.84 ± 0.07 30.23 ± 1.19
 6 123.40 ± 5.17 0.10 ± 0.00 119.30 ± 10.91 0.275 ± 0.006 0.053 ± 0.006 0.11 ± 0.01 1.85 ± 0.14 26.19 ± 1.29
Multiple dose
 1 16.01 ± 0.61 0.00 ± 0.00 13.15 ± 2.37 0.299 ± 0.011 0.086 ± 0.017 0.09 ± 0.01 1.62 ± 0.21 31.87 ± 0.18
 3 51.05 ± 4.59 0.18 ± 0.18 63.70 ± 21.34 0.378 ± 0.050 0.065 ± 0.015 0.09 ± 0.01 2.20 ± 0.37 34.77 ± 3.09
 6 105.52 ± 8.92 0.63 ± 0.26 158.43 ± 15.58 0.351 ± 0.016 0.043 ± 0.004 0.10 ± 0.00 3.53 ± 0.48 30.86 ± 0.96
a

All values represent the means ± standard errors of the means of values three rabbits each. Abbreviations: Cmin(24 h), plasma concentration at the end of the dosing interval (24 h); t1/2α distributional half-life; t1/2β, apparent elimination half-life; t1/2γ, terminal elimination half-life. 

b

P ⩽ 0.05 for the comparison among dosage groups by ANOVA.