Photodynamic inactivation of methicillin-resistant Staphylococcus aureus on skin using a porphyrinic formulation

Márcia Braz1, Diana Salvador1, Ana T P C Gomes1

  • 1Department of Biology & CESAM, University of Aveiro, 3810-193 Aveiro, Portugal.

Insights

Antimicrobial photodynamic therapy (aPDT) using a porphyrinic formulation effectively inactivates methicillin-resistant Staphylococcus aureus (MRSA) on skin. This approach shows promise for treating skin infections caused by antibiotic-resistant bacteria.

Area of Science:

  • Photomedicine
  • Dermatology
  • Microbiology

Background:

  • Staphylococcus aureus causes skin and soft tissue infections.
  • Increasing antibiotic resistance necessitates alternative treatments.
  • Methicillin-resistant Staphylococcus aureus (MRSA) poses a significant public health threat.

Purpose of the Study:

  • To evaluate the efficacy of antimicrobial photodynamic therapy (aPDT) with a porphyrinic formulation (FORM) for inactivating MRSA on skin.
  • To assess the potential of potassium iodide (KI) and iodopovidone (PVP-I) as potentiators of FORM in aPDT.

Main Methods:

  • The aPDT protocol was optimized in vitro using Phosphate Buffered Saline (PBS).
  • Porcine skin explants were artificially contaminated with MRSA and treated with FORM, FORM + KI, or FORM + PVP-I under white light.
  • MRSA inactivation was quantified by colony forming units (CFU) mL⁻¹.

Main Results:

  • FORM demonstrated efficacy in inactivating MRSA in vitro.
  • Combinations of FORM with KI or PVP-I significantly reduced irradiation time in vitro.
  • On porcine skin, FORM at 50 μM achieved a 3.1 Log₁₀ CFU mL⁻¹ reduction in MRSA.
  • Potentiation observed in vitro with KI and PVP-I was not replicated ex vivo on skin.

Conclusions:

  • aPDT with the porphyrinic formulation (FORM) is a promising strategy for MRSA inactivation on skin.
  • FORM alone demonstrates significant efficacy without the need for potentiating agents.
  • Further research may explore optimized formulations or delivery methods for enhanced ex vivo efficacy.