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. Author manuscript; available in PMC: 2010 Nov 9.
Published in final edited form as: Clin Pharmacol Ther. 2007 Jul 4;83(2):273–280. doi: 10.1038/sj.clpt.6100275

Table 4.

Metformin pharmacokinetic parameters from Oct1+/+ and Oct1−/− mice.

0ct1+/+ (n=5)
Octl−/− (n=6)
Mean SD Mean SD
T1/2 (h) 5.5 2.0 5.4 1.7
AUC0–1 h (μg h/ml) 3.1 0.57 4.0* 0.73
AUC0–24h (μg h/ml) 19.0 1.9 21.8 2.5
V/F (ml) 356 200 187 75
CL/F (ml/h) 29.7 6.0 23.6 4.5
Urine recovery (%) 60 7 50 13
Feces recovery (%) 30 10 29 3

AUC, area under the curve of blood concentration–time of metformin; CL/F, oral clearance (clearance over oral bioavailability); T1/2, half-life; V/F, oral volume of distribution (volume of distribution over oral bioavailability). The mice were given an oral dose of metformin (15mg/kg containing 0.2mCi/kg of 14C-metformin), approximating the single dose of 1,000mg in humans. The radioactivity in blood was determined and converted to mass amounts.

*

P=0.05 compared with Oct1+/+/ mice