Skip to main content
. 2022 Jul;63(7):727–734.

Table 1.

Pharmacokinetic parameters for flunixin meglumine and flunixin meglumine compounded with iron dextran determined by noncompartmental analysis in piglets.

Parameter Unit Flunixin meglumine
n = 8
Flunixin meglumine + Iron dextran
n = 8
AUC0–tlast h*μg/mL 18.21 ± 5.03 12.70 ± 2.88*
AUC0–∞ h*μg/mL 18.24 ± 5.03 12.72 ± 2.88*
t1/2 λz (HM) h 3.73 (LL 3.11, UL 4.66) 3.42 (LL 2.89, UL 4.19)
λz (HM) 1/h 0.17 (LL 0.14, UL 0.21) 0.19 (LL 0.16, UL 0.26)
CL/F mL/h/kg 129.19 ± 36.02 182.19 ± 48.65*
Cmax μg/mL 4.58 ± 0.74 3.22 ± 0.66*
Tmax h 0.57 (LL 0.36, UL 0.89) 0.68 (LL 0.43, UL 1.07)
VD/F mL/kg 750.10 ± 287.56 919.02 ± 245.44
MRT0–∞ (HM) h 3.89 (LL 3.43, UL 4.51) 3.92 (LL 3.45, UL 4.54)

AUC0–tlast — Area under the concentration time curve from time zero to last measured concentration; AUC0–∞ — AUC from time zero to infinity; t1/2λz — Elimination half-life; λz — Elimination rate constant; CL/F — Systemic clearance per fraction absorbed; Cmax — Maximum plasma concentration; Tmax — Time to maximal plasma concentration; VD/F — Volume of distribution per fraction absorbed; MRT0–∞ — Mean residence time from time zero to infinity. AUC0–tlast, AUC0–∞, CL/F, Cmax, and VD/F are expressed as mean ± SD. HM — Harmonic mean with 95% CI. Tmax is presented as median with lower and upper range limits.

*

Versus corresponding reference value (P < 0.05). n — Number of piglets per treatment group; LL — Lower limit; UL — Upper limit.