Preparation of gentamicin dioctyl sulfosuccinate loaded poly(trimethylene carbonate) matrices intended for the treatment of orthopaedic infections

G. A. ter Boo, D. W. Grijpma, R. G. Richards, T. F. Moriarty, D. Eglin*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

10 Citations (Scopus)

Abstract

BACKGROUND: Infection is a common problem in trauma and orthopaedic surgery. Antibiotic-loaded biomaterials are used locally to clear infections as an adjunct to systemic antibiotics. Gentamicin-sulphate (GEN-SULPH) is commonly used in antibiotic-loaded biomaterials, although it displays high water solubility resulting in quick diffusion from the carrier.

OBJECTIVE: Preparation of a lipophilic derivative of gentamicin to reduce solubility and obtain a slower release. Subsequently, entrapment of this lipophilic gentamicin within poly(trimethylene carbonate) (PTMC) matrices.

METHODS: Hydrophobic ion-pairing was used to prepare lipophilic gentamicin (GEN-AOT). The susceptibility of Staphylococcus aureus NCTC 12973 and Staphylococcus epidermidis 103.1 for GEN-AOT was tested and the viability of fibroblasts upon exposure to GEN-AOT was assessed. GEN-AOT was then loaded into PTMC films.

RESULTS: GEN-AOT was successfully prepared as confirmed by FTIR-spectroscopy. GEN-AOT was bactericidal for S. epidermidis and S. aureus at 0.5 mu M and 8.5 mu M, respectively. At 1.1 mu M GEN-AOT no reduction in fibroblast viability was observed. At 11 mu M the reduction was similar to 50%. PTMC discs loaded with GEN-AOT were prepared by compression molding.

CONCLUSIONS: Lipophilic GEN-AOT was at least as potent as GEN-SULPH. For S. epidermidis it was even more potent than GEN-SULPH. More than 50% fibroblast cell viability was maintained at bactericidal concentration for both bacterial strains.

Original languageEnglish
Pages (from-to)89-98
Number of pages10
JournalClinical hemorheology and microcirculation
Volume60
Issue number1
DOIs
Publication statusPublished - 2015

Keywords

  • Orthopaedic infection
  • local infection treatment
  • gentamicin
  • antibiotic modification
  • poly(trimethylene carbonate)
  • drug delivery
  • COLLAGEN
  • RELEASE
  • DEGRADATION
  • MANAGEMENT
  • DIAGNOSIS
  • DELIVERY
  • IMPLANT

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