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. Author manuscript; available in PMC: 2019 Oct 1.
Published in final edited form as: Eur J Drug Metab Pharmacokinet. 2018 Oct;43(5):543–554. doi: 10.1007/s13318-018-0464-z

Table 1.

Pharmacokinetic parameters of 14C-C3 in C57B6 mice

Parametera dose t1/2 AUC k Cl V Tmax Cmax
Units mg/kg hr μg-hr/mL 1/hr mL/kg-min l/kg min μg/mL
i.p. 1.1 8.0 ± 0.6 13.9 ± 1.4 0.087 ± 0.007 1.32 ± 0.13 0.91 ± 0.12 60 1.3 ± 0.1
i.v. 1.1 8.2 ± 0.2 15.2 ± 1.4 0.085 ± 0.002 1.20 ± 0.11 0.85 ± 0.08 5 4.0 ± 0.2
i.v.0-1b 1.1 0.8 ± 0.1 0.90 ± 0.12
p.o. 1.1 0.36 60 0.03
a

Parameters and formulas are described in the methods section.

b

values in the i.v.0-1 row are from data collected within the first hour after C3 injection. Values are mean ± SEM (n=6).

i.p. = intraperitoneal, i.v. = intravenous, and p.o. = per os,

AUC = area under the curve, Cl = systemic clearance, V= volume of distribution