ArticleThe Veterinary record2026
Effect of flunixin meglumine on the pharmacokinetics of enrofloxacin and marbofloxacin in preweaning calves.
Article in The Veterinary record, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundBovine respiratory disease is a major cause of illness in dairy calves. Fluoroquinolones such as enrofloxacin and marbofloxacin are commonly co-administered with flunixin meglumine, yet NSAID-related pharmacokinetic interactions in preweaning calves remain poorly defined. This study evaluated flunixin's effects on these drugs' pharmacokinetics and pharmacokinetic/pharmacodynamic (PK/PD) indices against key bovine respiratory pathogens of clinical relevance.
methodsTen healthy Holando Argentino calves (20-30 days old) received enrofloxacin (5 mg/kg intramuscularly) or marbofloxacin (6 mg/kg intramuscularly). After a 15-day washout period, calves received the same antimicrobial co-administered with flunixin meglumine (2.2 mg/kg intramuscularly). The plasma concentrations of the drugs in the first 24 hours after administration were measured using validated high-performance liquid chromatography, and non-compartmental analysis was performed to derive pharmacokinetic parameters. PK/PD indices were also calculated.
resultsFlunixin meglumine significantly prolonged the elimination half-life of both antimicrobials without modifying the area under the concentration-time curve from 0 to 24 hours. It also reduced the biotransformation of enrofloxacin to ciprofloxacin. PK/PD targets were achieved for Pasteurella multocida and Histophilus somni but not for Mannheimia haemolytica or Mycoplasma bovis. LIMITATIONS: The study was limited by the use of clinically healthy calves only, the small sample size, reliance on published minimum inhibitory concentration values and plasma-based PK/PD analysis.
conclusionFlunixin prolongs elimination of enrofloxacin and marbofloxacin without compromising estimated efficacy, although optimisation may be required for some bovine respiratory disease pathogens.
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