Skip to main content
. 2013 Nov;51(11):3547–3554. doi: 10.1128/JCM.01498-13

Table 1.

Oral doxycycline pharmacokinetics in dogs

Source No. of subjects Dose (mg/kg) Mean ± SDa
t1/2 (h) kel (h−1) Vd/F (liters/kg) CL/F (liters/kg/h) AUC (μg·h/ml) Cmax (μg/ml) Absorption t1/2 (h) Tmax (h) F (%)
van Gool et al. (11) 4 10 8.34 ± 2.77 0.0831 ± 0.0277 1.28 ± 0.5 0.1 ± 0.02 NR 4.03 ± 1.25 0.87 ± 0.4 3.04 ± 1.15 57.3 ± 17.2
Gutierrez et al. (10) 12 10 5.59 ± 0.03 0.124 ± 0.0007 1.49 ± 0.27 0.137 ± 0.012 72.89 ± 6.3 5.58 ± 0.5 1.49 ± 0.07 3.88 ± 0.4 74.88
Dominguez et al. (presented at the American Academy of Veterinary Pharmacology and Therapeutics 18th Biennial Symposium) 5 10 NR NR NR 0.215 ± 0.065 NR NR NR NR NR
Rogar (unpublished data) 6 5.023 29.496 ± 6.15 0.0235 ± 0.0049 2.299 ± 1.333 0.0676 ± 0.035 92.962 ± 53.89 3.968 ± 3.904 NR 4.125 ± 2.326 53.36 ± 28.57
Overall mean ± SD 14.475 ± 3.066 0.077 ± 0.015 1.690 ± 0.559 0.102 ± 0.012 82.926 ± 33.651 4.526 ± 1.789 1.180 ± 0.233 3.682 ± 0.971 61.847 ± 8.040
Weighted mean ± SD 27 12.61 ± 11.10 1.67 ± 0.81 0.131 ± 0.061
a

t1/2, terminal half-life; kel, terminal rate constant; Vd/F, apparent volume of distribution per fraction absorbed; CL/F, systemic clearance per fraction absorbed; AUC, area under the curve; Cmax, maximal (peak) plasma concentration; absorption t1/2, half-life for oral absorption; Tmax, time to peak concentration; F, fraction of oral dose absorbed; NR, not reported in the study. Weighted means and standard deviations (described in more detail in the text) account for weighted differences in the numbers of subjects per study and within-study variations. Weighted means were calculated only for parameters that were necessary for Monte Carlo simulations.