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. 1999 Oct;43(10):2345–2349. doi: 10.1128/aac.43.10.2345

TABLE 1.

Pharmacokinetic dataa

Administration Site AUC (μg · h · ml−1) Cmax (μg · ml−1) Tmax (h) t1/2 (h) Clearance (liter · h−1)
I.v. Plasma 22.9 ± 11.1 3.7 ± 0.7 1.0 ± 0.2 14.3 ± 2.4 2.3 ± 0.4
Muscle 9.5 ± 5.9* 1.2 ± 0.8 1.8 ± 0.6
Subcutis 7.9 ± 4.6* 1.0 ± 0.5 2.0 ± 1.0
Saliva 21.4 ± 5.0 5.1 ± 1.4 1.0 ± 0.1 14.9 ± 2.7
Capillary 22.1 ± 2.0 4.2 ± 0.4 1.0 ± 0.0 12.3 ± 2.1
Blister 16.7 ± 4.1 1.7 ± 0.3 5.6 ± 4.5
P.o. Plasma 19.8 ± 1.5 3.2 ± 0.6 1.6 ± 0.8 14.3 ± 2.0 2.4 ± 0.4
Muscle 8.5 ± 2.0* 0.9 ± 0.2 3.2 ± 1.4 10.2 ± 1.7
Subcutis 8.0 ± 2.1* 0.9 ± 0.2 2.4 ± 1.7 7.5 ± 2.6
Saliva 17.6 ± 2.7 3.6 ± 1.0 1.7 ± 0.7 14.3 ± 3.2
Capillary 18.7 ± 3.1 2.7 ± 0.8 2.5 ± 3.3 12.0 ± 2.2
Blister 12.3 ± 3.3* 1.6 ± 0.2 8.0 ± 3.7
a

Pharmacokinetic parameters for venous plasma (0 to 12 h), skeletal muscle and subcutaneous adipose interstitial fluid (0 to 12 h), saliva (0 to 12 h), capillary plasma (0 to 12 h), and cantharides-induced skin blister fluid (0 to 12 h) following administration of moxifloxacin (single i.v. dose of 400 mg over 60 min or p.o. dose of 400-mg tablet) in healthy volunteers (n = 12). The results are presented as means ± SD. *, P < 0.05 versus AUCplasma