Usnic acid-loaded biocompatible magnetic PLGA-PVA microsphere thin films fabricated by MAPLE with increased

V Grumezescu1, A M Holban, A M Grumezescu

  • 1Department of Science and Engineering of Oxide Materials and Nanomaterials, Faculty of Applied Chemistry and Materials Science, University Politehnica of Bucharest, Polizu Street no 1-7, 011061 Bucharest, Romania. Lasers Department, Plasma and Radiation Physics, National Institute for Lasers, PO Box MG-36, Bucharest-Magurele, Romania.

Biofabrication
|April 12, 2014
PubMed

Insights

This study developed a novel coating using (+)-usnic acid (UA)-loaded microspheres to combat Staphylococcus aureus biofilms. The bio-nano-active surface effectively inhibited bacterial attachment and biofilm development, offering a promising solution for preventing hospital-acquired infections.

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Microbiology

Background:

  • Staphylococcus aureus biofilm infections are persistent and resistant to current therapies, causing significant morbidity and mortality.
  • Developing effective strategies to control S. aureus colonization is crucial for healthcare settings.
  • (+)-usnic acid (UA) exhibits antimicrobial properties against Gram-positive bacteria, including S. aureus.

Purpose of the Study:

  • To create a bio-nano-active surface using UA-loaded microspheres for controlling S. aureus biofilm formation.
  • To evaluate the efficacy of UA-loaded PLGA-PVA microsphere coatings in preventing S. aureus attachment and biofilm development.
  • To assess the biocompatibility of the fabricated thin films for potential biomedical applications.

Main Methods:

  • Loading magnetic polylactic-co-glycolic acid-polyvinyl alcohol (PLGA-PVA) microspheres with (+)-usnic acid (UA).
  • Fabricating thin coatings using matrix-assisted pulsed laser evaporation of UA-loaded microspheres.
  • Quantitatively assessing S. aureus biofilm formation on coated surfaces using culture-based assays.
  • Performing in vitro bioevaluation tests to determine biocompatibility.

Main Results:

  • The UA-loaded microsphere coatings significantly inhibited the initial attachment of S. aureus.
  • The developed surfaces effectively prevented the development of mature S. aureus biofilms.
  • In vitro tests demonstrated excellent biocompatibility of the fabricated thin films.

Conclusions:

  • UA-loaded PLGA-PVA microsphere coatings represent a promising strategy for developing non-toxic, S. aureus-resistant surfaces.
  • These coatings show potential for preventing hospital-acquired infections and reducing biofilm-associated morbidity.
  • The biocompatible nature of the films suggests applications in stem cell cultivation and tissue engineering scaffolds.