Pharmacokinetics and distribution of minocycline in mature horses after oral administration of multiple doses and comparison with minimum inhibitory concentrations

• Published in: Equine veterinary journal 2012-07, Vol.44 (4), p.453-458
• Main Authors: SCHNABEL, L. V., PAPICH, M. G., DIVERS, T. J., ALTIER, C., APREA, M. S., McCARREL, T. M., FORTIER, L. A.
• Format: Article
• Language: English
• Subjects: Administration, Oral; Animals; Anti-Bacterial Agents - administration & dosage; Anti-Bacterial Agents - pharmacokinetics; Aqueous Humor - chemistry; aqueous humour; Area Under Curve; Bacteria - drug effects; cerebral spinal fluid; Drug Administration Schedule; Female; Half-Life; horse; Horses - blood; Horses - cerebrospinal fluid; Horses - metabolism; Male; Medical research; Microbial Sensitivity Tests; minimum inhibitory concentrations; minocycline; Minocycline - administration & dosage; Minocycline - chemistry; Minocycline - pharmacokinetics; pharmacokinetics; Pilot Projects; synovial fluid; Synovial Fluid - chemistry; Tissue Distribution
• ISSN: 0425-1644; 2042-3306
• DOI: 10.1111/j.2042-3306.2011.00459.x

Summary Reasons for performing study: Minocycline holds great potential for use in horses not only for its antimicrobial effects but also for its anti‐inflammatory and neuroprotective properties. However, there are no pharmacokinetic or safety data available regarding the use of oral minocycline in horses. Objectives: To determine pharmacokinetics, safety and penetration into plasma, synovial fluid, aqueous humour (AH) and cerebral spinal fluid (CSF) of minocycline after oral administration of multiple doses in horses and to determine the minimum inhibitory concentrations (MIC) of minocycline for equine pathogenic bacteria. Methods: Six horses received minocycline (4 mg/kg bwt q. 12 h for 5 doses). Thirty‐three blood and 9 synovial fluid samples were collected over 96 h. Aqueous humour and CSF samples were collected 1 h after the final dose. Minocycline concentrations were measured using high pressure liquid chromatography. The MIC values of minocycline for equine bacterial isolates were determined. Results: At steady state, the mean ± s.d. peak concentration of minocycline in the plasma was 0.67 ± 0.26 µg/ml and the mean half‐life was 11.48 ± 3.23 h. The highest trough synovial fluid minocycline concentration was 0.33 ± 0.12 µg/ml. The AH concentration of minocycline was 0.09 ± 0.03 µg/ml in normal eyes and 0.11 ± 0.04 µg/ml in blood aqueous barrier‐disrupted eyes. The mean CSF concentration of minocycline was 0.38 ± 0.09 µg/ml. The MIC values were determined for 301 isolates. Minocycline concentrations were above the MIC50 and MIC90 for many gram‐positive equine pathogens. Potential relevance: This study supports the use of orally administered minocycline at a dose of 4 mg/kg bwt every 12 h for the treatment of nonocular infections caused by susceptible (MIC≤0.25 µg/ml) organisms in horses. Further studies are required to determine the dose that would be effective for the treatment of ocular infections.