Efficacy of Cold Atmospheric Plasma Against Methicillin-Resistant Staphylococcus aureus Biofilms: A Systematic Review

Reyhaneh Shoorgashti1, Faezeh Dehghan Ghanatkaman2, Sana Baghizadeh2

  • 1Researcher, Department of Oral Medicine, TeMS. C., Islamic Azad University, Tehran, Iran, azad.ac.ir.

Abstract

Insights

Cold atmospheric plasma effectively reduces methicillin-resistant Staphylococcus aureus biofilms in vitro. This technology shows promise as an adjunctive treatment for biofilm infections, potentially overcoming antibiotic resistance.

Area of Science:

  • Microbiology
  • Biophysics
  • Materials Science

Background:

  • Methicillin-resistant Staphylococcus aureus (MRSA) presents a significant global health challenge due to antibiotic resistance and robust biofilm formation.
  • Cold atmospheric plasma (CAP) is an emerging technology with potential for inactivating microbial biofilms.

Purpose of the Study:

  • To systematically evaluate the in vitro efficacy of CAP in disrupting or eradicating MRSA biofilms.
  • To identify factors influencing CAP treatment outcomes for MRSA biofilms.

Main Methods:

  • A comprehensive literature search was performed across five major databases for in vitro studies up to July 2025.
  • Studies assessing CAP effects on MRSA biofilms were included, with data extracted on device parameters, exposure conditions, and microbial outcomes.
  • Risk of bias was assessed using a modified ToxRTool.

Main Results:

  • Seventeen in vitro studies were included, predominantly using dielectric barrier discharge and plasma jet devices with air-based plasmas.
  • All studies reported significant reductions in MRSA biofilm load (log10 CFU reductions from 1 to >6), influenced by exposure time, surface material, and device.
  • Near-complete biofilm eradication was achieved within minutes in several studies, with observed synergistic effects when CAP was combined with antibiotics.

Conclusions:

  • Cold atmospheric plasma demonstrates potential as an adjunctive strategy for controlling biofilm-related infections.
  • Further standardized and clinically relevant research is necessary to fully establish CAP's role in infection control.

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