Polymer-Based Local Antibiotic Delivery for Prevention of Polymicrobial Infection in Contaminated Mandibular Implants

Sarita R Shah1, Alexander M Tatara1, Johnny Lam1

  • 1Department of Bioengineering, Rice University, Houston, Texas 77030, United States.

Insights

Porous poly(methyl methacrylate) (PMMA) space maintainers releasing clindamycin demonstrated that antibiotic release speed and dose impact tissue healing. Burst release formulations promoted better bone and soft tissue healing than extended release, independent of bacterial clearance.

Area of Science:

  • Biomaterials Science
  • Regenerative Medicine
  • Oral and Maxillofacial Surgery

Background:

  • Porous poly(methyl methacrylate) (PMMA) space maintainers facilitate local antibiotic delivery and tissue integration.
  • Poly(DL-lactic-co-glycolic acid) (PLGA) is utilized as a carrier for antibiotic elution.
  • Investigating the impact of antibiotic release kinetics and dosage on healing is crucial for optimizing these devices.

Purpose of the Study:

  • To evaluate the effect of clindamycin release kinetics and dose from PMMA space maintainers on bacterial clearance and tissue healing.
  • To compare burst release versus extended release formulations in a rabbit mandibular defect model.
  • To determine if antibiotic release influences healing outcomes independently of bacterial eradication.

Main Methods:

  • Fabrication of clindamycin-loaded PMMA space maintainers with varying release profiles (burst vs. extended) and doses.
  • Implantation into pathogen-contaminated rabbit mandibular defects.
  • Histological analysis to assess inflammation, fibrous capsule formation, and bone regeneration.

Main Results:

  • No recovery of inoculated bacteria across all specimen groups.
  • Burst release formulation exhibited reduced inflammation and fibrous capsule formation compared to low-dose extended release.
  • Burst release formulation demonstrated enhanced bone formation adjacent to the implant relative to low-dose extended release.

Conclusions:

  • Local antibiotic release kinetics and dose significantly influence soft and hard tissue healing.
  • These effects appear to be independent of the formulation's ability to clear bacteria.
  • Optimizing release profiles of antibiotic-eluting devices is critical for regenerative outcomes.