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. 2011 May;55(5):1975–1981. doi: 10.1128/AAC.01627-10

Table 4.

Pharmacokinetic parameters after i.v. and p.o. dosing of CD1 micea

Cyclophilin inhibitor Clearance (liter/h/kg) t1/2 (h) Vss (liter/kg) AUClastb (h · ng/ml)
p.o. Cmaxc (ng/ml) F (%)
I.v. P.o.
SfA 0.054 8.02 0.522 16,473 2,332 192 1.42
SfB 0.068 5.89 0.439 14,067 5,693 809 3.94
SfC 0.824 1.11 0.383 1,257 26 22 0.21
SfD 0.545 1.64 0.244 2,157 20 12 0.09
a

Data were generated after analysis of whole-blood samples, following doses of 1 mg/kg i.v. and 10 mg/kg p.o. to CD1 mice.

b

AUClast, area under the concentration-time curve.

c

Cmax, maximum concentration of drug in serum.