Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Mar;48(2):103-109.
doi: 10.1111/jvp.13481. Epub 2024 Sep 15.

Pharmacokinetics and Plasma Protein Binding of Flunixin in Rainbow Trout (Oncorhynchus mykiss)

Affiliations

Pharmacokinetics and Plasma Protein Binding of Flunixin in Rainbow Trout (Oncorhynchus mykiss)

Kamil Uney et al. J Vet Pharmacol Ther. 2025 Mar.

Abstract

Flunixin's pharmacokinetics, bioavailability, and plasma protein binding were examined in rainbow trout. The experiment involved 252 rainbow trout (Oncorhynchus mykiss) maintained at 12 ± 0.6°C. Flunixin was administered to rainbow trout via intravascular (IV), intramuscular (IM), and oral routes at a dosage of 2.2 mg/kg. Plasma samples were collected at times 0 (control), 0.25, 0.5, 1, 2, 4, 6, 8, 10, 12, 24, 48, 72, and 96 h. High-pressure liquid chromatography-ultraviolet was employed to quantify flunixin concentrations. The elimination half-life (t1/2ʎz) for flunixin was 8.37 h for IV, 8.68 h for IM, and 8.76 h for oral. The t1/2ʎz was similar between administration groups. The volume of distribution at a steady state and total body clearance were 55.81 mL/kg and 6.83 mL/h/kg, respectively, after IV administration. The mean peak plasma concentration was 6.24 ± 0.41 μg/mL at 4 h for oral administration and 13.98 ± 0.86 μg/mL at 2 h for IM administration. The in vitro protein binding ratio of flunixin in rainbow trout plasma was 96.34 ± 2.29%. The bioavailability of flunixin after oral (25.74%) administration was lower than that after IM (66.70%) administration. Thus, developing an oral pharmaceutical formulation that can be administered with feed and has high bioavailability could enhance the therapeutic effect.

Keywords: bioavailability; flunixin; pharmacokinetics; plasma protein binding; rainbow trout.

PubMed Disclaimer

References

    1. Anderson, K. L., C. A. Neff‐Davis, L. E. Davis, and V. D. Bass. 1990. “Pharmacokinetics of Flunixin Meglumine in Lactating Cattle After Single and Multiple Intramuscular and Intravenous Administrations.” American Journal of Veterinary Research 51, no. 9: 1464–1467.
    1. Bowser, P. R., and J. G. Babish. 1991. “Clinical Pharmacology and Efficacy of Fluoroquinolones in Fish.” Annual Review of Fish Diseases 1: 63–66.
    1. Brown, L. A., J. Ainsworth, M. Beleau, et al. 1986. “In the Effects of Tricaine Methanesulphonate, Flunixin Meglumine and Metomidate on Serum Cortisol in Channel Catfish (Ictalurus punctatus; Rafinesque).” In IAAAM Archive Proceedings. Proceedings of the International Association for Aquatic Animal Medicine, Gulfport, MS, USA, 33.
    1. Chatigny, F., C. M. Creighton, and E. D. Stevens. 2018. “Updated Review of Fish Analgesia.” Journal of the American Association for Laboratory Animal Science 57: 5–12.
    1. Cheng, Z., Q. McKeller, and A. Nolan. 1998. “Pharmacokinetic Studies of Flunixin Meglumine and Phenylbutazone in Plasma, Exudate and Transudate in Sheep.” Journal of Veterinary Pharmacology and Therapeutics 21, no. 4: 315–321.

MeSH terms

LinkOut - more resources