Innovative microparticle strategies: harnessing essential oil-loaded lecithin/chitosan systems against Burkholderia

Anderson da Cunha Costa1,2, Dayana Pinto de Meneses3, Maria Rosiene Antunes Arcanjo3

  • 1Department of Pathology and Legal Medicine, School of Medicine, One Health Microbiology Laboratory, Postgraduate Program in Medical Sciences, Federal University of Ceará, Fortaleza, CE, Brazil.

Biofouling
|February 24, 2026
PubMed

Insights

Novel lecithin/chitosan microparticles loaded with lemongrass (LEO) and geranium (GEO) essential oils show dual antimicrobial and antibiofilm activity against Burkholderia pseudomallei. These microparticles (LEOLCN and GEOLCN) enhance antibiotic efficacy, offering a promising strategy against melioidosis.

Area of Science:

  • Microbiology
  • Materials Science
  • Pharmacology

Background:

  • Burkholderia pseudomallei causes melioidosis and exhibits high antimicrobial resistance.
  • Biofilm formation is a key factor contributing to B. pseudomallei's resistance.
  • Novel strategies are needed to overcome antimicrobial resistance in B. pseudomallei infections.

Purpose of the Study:

  • To develop and characterize lecithin/chitosan microparticles loaded with lemongrass (LEO) and geranium (GEO) essential oils.
  • To evaluate the antimicrobial and antibiofilm activity of these microparticles against B. pseudomallei.
  • To investigate the synergistic effects of microparticles with conventional antibiotics.

Main Methods:

  • Synthesis and characterization of LEO/GEO-loaded lecithin/chitosan microparticles (LEOLCN, GEOLCN).
  • Evaluation of planktonic growth inhibition (MICs) and biofilm inhibition assays.
  • Assessment of synergistic interactions with antibiotics (ceftazidime) and scanning electron microscopy (SEM) for biofilm disruption.

Main Results:

  • Microparticles showed spherical morphology, high encapsulation efficiency, and sustained release profiles.
  • LEOLCN and GEOLCN demonstrated significant antibiofilm activity, reducing biomass and metabolic activity by over 50%.
  • LEOLCN exhibited synergistic effects with ceftazidime, reducing MICs 2- to 9-fold, and SEM confirmed biofilm disruption.

Conclusions:

  • LEOLCN and GEOLCN microparticles possess dual antimicrobial and antibiofilm properties against B. pseudomallei.
  • These microparticles represent a promising platform to enhance antibiotic therapy against resistant strains.
  • The developed microparticles offer an innovative in vitro strategy to combat persistent B. pseudomallei infections and biofilm resistance.