In vitro antibacterial activity of bioactive glass S53P4 on multiresistant pathogens causing osteomyelitis and

Mateus Trinconi Cunha1, Maria Aparecida Murça2, Stanley Nigro2

  • 1Division of Infectious Diseases, Department of Internal Medicine, Santa Casa de São Paulo School of Medical Sciences, São Paulo, Brazil.

Abstract

Insights

Bioactive Glass S53P4 demonstrates comparable in vitro antibacterial activity to antibiotic-loaded polymethylmethacrylate for multidrug-resistant bacteria. This finding suggests BAG S53P4 as a viable alternative for treating osteomyelitis and prosthetic joint infections.

Area of Science:

  • Biomaterials Science
  • Infectious Diseases
  • Orthopedic Surgery

Background:

  • Conventional treatment for medullary osteomyelitis involves antibiotic-loaded polymethylmethacrylate (PMMA) cement.
  • PMMA may deliver inconsistent antibiotic concentrations to surrounding tissues.
  • Bioactive Glass (BAG) S53P4 exhibits local antibacterial activity.

Purpose of the Study:

  • To compare the in vitro antibacterial activity of BAG S53P4 against antibiotic-loaded PMMA.
  • To evaluate efficacy against multidrug-resistant (MDR) bacteria isolated from osteomyelitis (OM) and prosthetic joint infections (PJI).

Main Methods:

  • Convenience samples of MDR microorganisms from OM and PJI patients were used.
  • In vitro antibacterial activity was assessed using time-kill curves.
  • BAG S53P4 granules and antibiotic-loaded PMMA beads were tested against MRSA, MR-CoNS, P. aeruginosa, and K. pneumoniae.

Main Results:

  • Both BAG S53P4 and antibiotic-loaded PMMA inhibited bacterial growth, reaching zero CFU/ml between 120 and 168 hours.
  • No significant difference in time-kill curves was observed between BAG S53P4 and antibiotic-loaded PMMA.
  • Bacterial inhibition was significantly greater than with inert glass controls (p < 0.05).

Conclusions:

  • BAG S53P4 possesses comparable antibacterial properties to antibiotic-loaded PMMA against MDR bacteria.
  • BAG S53P4 is a potential alternative for treating OM and PJI caused by MDR bacteria.

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