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. 2001 Dec;45(12):3322–3327. doi: 10.1128/AAC.45.12.3322-3327.2001

TABLE 2.

Multiple-dose compartmental pharmacokinetic parameters of micafungin in plasmaa

Drug dose (mg/kg) Cmax (μg/ml) Cmin (μg/ml) AUC0–∞ (μg  ·  h/ml) Vp (liter/kg) Vc (liter/kg) VSS (liter/kg) CLd (liter/h/kg) CLt (liter/h/kg) α-HL (h) β-HL (h)
0.5 9.443 ± 1.83 <LLQ 6.22 ± 0.97 0.226 ± 0.053 0.031 ± 0.004 0.258 ± 0.057 0.182 ± 0.085 0.075 ± 0.012 0.07 ± 0.006 2.988 ± 0.424
1.0 18.093 ± 1.19 <LLQ 14.16 ± 2.11 0.215 ± 0.02 0.029 ± 0.002 0.245 ± 0.02 0.235 ± 0.009 0.067 ± 0.01 0.063 ± 0.002 3.178 ± 0.192
2.0 19.165 ± 0.305 <LLQ 22.29 ± 1.76 0.223 ± 0.011 0.090 ± 0.011 0.313 ± 0.007 0.393 ± 0.043 0.083 ± 0.009 0.101 ± 0.011 3.347 ± 0.447
P valueb 0.0096 NA 0.0040 0.9774 0.0002 0.5479 0.0306 0.9227 0.0222 0.7995
a

All values represent the means ± SEMs of 3 rabbits each. Abbreviations: Vp and Vc, volume of distribution of the peripheral and central compartment, respectively; CLd, distributional clearance; α-HL, distributional half-life; β-HL, elimination half-life; NA, not applicable. The LLQ of the analytical assay was 0.1 μg/ml. 

b

P  values for the comparison among dosage groups by ANOVA.