Tissue concentrations of vancomycin and Moxifloxacin in periprosthetic infection in rats

Johannes Beckmann1, Frieder Kees, Jens Schaumburger

  • 1Department of Orthopedic Surgery, Institute of Medical Microbiology and Hygiene, University of Regensburg, Landshut, Germany. j.beckmann@asklepios.com

Acta Orthopaedica
|February 1, 2008
PubMed
Abstract

Insights

Moxifloxacin achieved higher tissue concentrations than vancomycin in a rat model of periprosthetic infection. This antibiotic distribution is crucial for effective treatment of bone infection and endoprosthesis complications.

Area of Science:

  • Pharmacology
  • Infectious Diseases
  • Orthopedic Surgery

Background:

  • Periprosthetic infection necessitates high antibiotic concentrations at the endoprosthesis site for effective treatment.
  • Evaluating antibiotic tissue distribution is critical for managing such infections.

Purpose of the Study:

  • To compare the tissue distribution of vancomycin and Moxifloxacin in a rat model of periprosthetic infection.
  • To assess the efficacy of these antibiotics in achieving therapeutic concentrations in infected tissues.

Main Methods:

  • A standardized in vivo model of periprosthetic infection was established in 36 male rats.
  • Animals received vancomycin, Moxifloxacin, or sham treatment for two weeks.
  • Antibiotic concentrations in plasma and various tissues (lung, muscle, fat, bone) were measured post-treatment.

Main Results:

  • Moxifloxacin demonstrated significantly higher tissue concentrations and tissue-plasma ratios compared to vancomycin across all evaluated tissues.
  • Moxifloxacin concentrations remained consistent in both infected and uninfected hind legs.
  • Vancomycin concentrations were notably higher in the infected hind leg compared to the uninfected leg.

Conclusions:

  • The developed rat model is suitable for evaluating antibiotic efficacy and tissue distribution in periprosthetic infections.
  • Findings suggest Moxifloxacin's favorable tissue penetration may offer advantages in treating periprosthetic infections.
  • This model can be adapted for future studies investigating various pathogens, antibiotics, and treatment regimens to correlate tissue concentrations with clinical outcomes.