[Studies on suppurative lesion and bone distribution of peroral antimicrobial agents (LAPC and TFLX) to experimental

M Tanaka1, T Satoh

  • 1Department of Oral and Maxillofacial Surgery I, Nippon Dental University School of Dentistry at Tokyo.

Shigaku = Odontology; Journal of Nihon Dental College
|October 1, 1990
PubMed

Insights

Lenamipicillin (LAPC) and tosufloxacin tosilate (TFLX) showed higher concentrations in infected rabbit mandibles and pus compared to healthy subjects. Both antibiotics effectively diffused to infection sites, indicating promising clinical efficacy for treating mandibular infections.

Area of Science:

  • Pharmacology
  • Infectious Diseases
  • Oral Surgery

Context:

  • Mandibular infections pose significant clinical challenges.
  • Accurate drug delivery to infection foci is crucial for treatment success.
  • Animal models are essential for preclinical evaluation of antimicrobial agents.

Purpose:

  • To evaluate the pharmacokinetics and tissue distribution of lenamipicillin (LAPC) and tosufloxacin tosilate (TFLX) in a rabbit mandibular infection model.
  • To compare drug concentrations in serum, pus, bone, and organs between infected and healthy rabbits.
  • To assess the diffusion of LAPC and TFLX into purulent exudate.

Summary:

  • Infection models in rabbit mandibles were established using *Streptococcus milleri* and *Bacteroides fragilis*.
  • LAPC and TFLX concentrations were significantly higher in serum and bone tissues of infected rabbits compared to healthy controls.
  • Both antibiotics demonstrated superior diffusion into pus compared to serum, with favorable Cmax and AUC ratios.

Impact:

  • The findings suggest that both LAPC and TFLX achieve satisfactory concentrations at local infection sites in the mandible.
  • Systemic diffusion and local accumulation of these antibiotics indicate potential for effective clinical treatment of mandibular osteomyelitis.
  • This study provides valuable pharmacokinetic data supporting the use of LAPC and TFLX in treating similar oral and maxillofacial infections.

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