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Combination of bacteriophages and vancomycin in a co-delivery hydrogel for localized treatment of fracture-related infections

  • Baixing Chen,
  • Luis Ponce Benavente,
  • Marco Chittò,
  • Virginia Post,
  • Caroline Constant,
  • Stephan Zeiter,
  • Pamela Nylund,
  • Matteo D’Este,
  • Mercedes González Moreno,
  • Andrej Trampuz,
  • Jeroen Wagemans,
  • Rob Lavigne,
  • Jolien Onsea,
  • R. Geoff Richards,
  • Willem-Jan Metsemakers,
  • T. Fintan Moriarty

摘要

Fracture-related infections (FRIs), particularly those caused by methicillin-resistant Staphylococcus aureus (MRSA), are challenging to treat. This study designed and evaluated a hydrogel loaded with a cocktail of bacteriophages and vancomycin (1.2 mg/mL). The co-delivery hydrogel showed 99.72% reduction in MRSA biofilm in vitro. The hydrogel released 54% of phages and 82% of vancomycin within 72 h and maintained activity for eight days, in vivo the co-delivery hydrogel with systemic antibiotic significantly reduced bacterial load by 0.99 log10 CFU compared to controls, with active phages detected in tissues at euthanasia (2 × 103 PFU/mL). No phage resistance was detected in the phage treatment groups, and serum neutralization resulted in only a 20% reduction in phage count. In this work, we show that a phage-antibiotic co-delivery system via CMC hydrogel is a promising adjunct to systemic antibiotic therapy for MRSA-induced FRI, highlighting its potential for localized, sustained delivery and improved treatment outcomes.