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. 2016 Jan 20;10:357–370. doi: 10.2147/DDDT.S95934

Table 1.

Pharmacokinetic characteristics of nemonoxacin in 12 healthy Chinese volunteers after a single oral dose of 500 mg of nemonoxacin alone or with probenecid

Parameters Nemonoxacin alone (Treatment A) Nemonoxacin with probenecid (Treatment B) Geometric mean ratio (B:A)a
AUC0−t, h·μg/mL 46.3 (7.4) 58.7 (11.5) 1.25 (1.19–1.32)
AUC0−∞, h·μg/mL 46.5 (7.5) 58.4 (11.5) 1.25 (1.19–1.32)
Cmax, μg/mL 5.67 (7.04) 5.76 (1.04) 1.01 (0.96–1.06)
tmax, h 1 (0.67–3.0)b 1.5 (0.67–4.0)b
t1/2, h 9.76 (0.74) 9.62 (0.74)
MRT, h 9.24 (0.51) 11.1 (0.9)
CL/F, L/h 11.0 (1.8) 8.83 (1.77)
Vz/F, L 155 (31) 123 (31)
Fe, % 58.2 (9.4) 56.5 (7.1) 0.96 (0.88–1.03)
CLr, L/h 6.41 (1.85) 4.96 (1.10) 0.76 (0.71–0.82)

Note: Data are mean (standard deviations), except

a

point estimates (90% confidence intervals) and

b

medians (ranges). The dash indicates no data available.

Abbreviations: AUC0−∞, area under the plasma concentration–time curve from time 0 to infinity; AUC0−t, area under the plasma concentration time curve from time 0 to the last time point; Cmax, maximum concentration; CL/F, oral clearance; CLr, renal clearance; Fe, percentage of the administered dose recovered in the urine; MRT, mean residence time; t1/2, terminal elimination half-life; tmax, time to reach Cmax; Vz/F, terminal volume of distribution without correction for bioavailability.