Antibiotic-eluting hydrophilized PMMA bone cement with prolonged bactericidal effect for the treatment of

Eun Jo Oh1, Se Heang Oh2, In Soo Lee3

  • 1Department of Advanced Materials, Hannam University, Daejeon, Republic of Korea.

Insights

This study developed novel bone cement for osteomyelitis treatment. The new Pluronic F68-enhanced cement effectively released antibiotics and inhibited bacterial growth in animal models.

Area of Science:

  • Biomaterials Science
  • Orthopedic Surgery
  • Infectious Disease Treatment

Background:

  • Osteomyelitis presents a significant challenge in orthopedic surgery.
  • Current treatments face limitations despite advancements in surgical and pharmaceutical approaches.

Purpose of the Study:

  • To develop and evaluate hydrophilized poly(methyl methacrylate) (PMMA) bone cements with sustained antibiotic release for osteomyelitis treatment.
  • To assess the mechanical properties, antibiotic elution profile, antibacterial efficacy, and in vivo performance of the novel bone cement.

Main Methods:

  • Preparation of PMMA bone cements incorporating Pluronic F68 and vancomycin.
  • Evaluation of compressive strength, antibiotic release kinetics (up to 11 weeks), and antibacterial activity against S. aureus (zone of inhibition).
  • Assessment of cytotoxicity and efficacy in a rat femoral osteomyelitis model.

Main Results:

  • PMMA bone cements with <7 wt% Pluronic F68 showed comparable mechanical properties to control VAcement.
  • The 7 wt% Pluronic F68-vancomycin cement demonstrated sustained antibiotic release for 11 weeks with nearly 100% elution.
  • This cement exhibited significant antibacterial activity against S. aureus for six weeks and proved effective in an animal model without notable cytotoxicity.

Conclusions:

  • Pluronic F68 as a hydrophilic additive in vancomycin-eluting PMMA bone cement is a promising strategy for osteomyelitis treatment.
  • The developed F68-VAcement offers sustained antibiotic delivery and potent antibacterial effects, addressing a critical clinical need.

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