Poly(vinyl alcohol)/Polycaprolactone Nanofiber Enriched with Lichenysin against Multidrug-Resistance Bacterial

Swati Yadav1, Dilip Kumar Arya1, Shubham Kanaujiya1

  • 1Department of Pharmaceutical Sciences, Babasaheb Bhimrao Ambedkar University, Lucknow 226025, India.

PubMed

Insights

This study developed Lichenysin (LCN)-loaded poly(vinyl alcohol)/polycaprolactone nanofiber scaffolds for treating multidrug-resistant infectious wounds. These scaffolds show promise for enhanced wound healing in diabetic rats.

Area of Science:

  • Biomaterials Science
  • Infectious Diseases
  • Regenerative Medicine

Background:

  • Multidrug resistance (MDR) in wound infections increases patient morbidity.
  • Lichenysin (LCN), a biosurfactant from *Bacillus licheniformis*, exhibits potent antimicrobial properties.
  • Developing effective treatments for MDR wound infections, especially in diabetic patients, is critical.

Purpose of the Study:

  • To fabricate and evaluate Lichenysin (LCN)-incorporated poly(vinyl alcohol)/polycaprolactone (PVA/PCL) nanofiber scaffolds.
  • To assess the potential of these LCN-loaded scaffolds as a biomaterial for treating multidrug-resistant infectious wounds.
  • To investigate the efficacy in a diabetic rat model.

Main Methods:

  • Electrospinning was used to create LCN-loaded PVA/PCL nanofiber scaffolds.
  • Scaffolds were characterized using SEM, FTIR, XRD, mechanical testing, and degradation studies.
  • Antimicrobial activity, in vitro cytotoxicity (L-929 cells), hemocompatibility, and in vivo wound healing in diabetic rats were evaluated.

Main Results:

  • SEM confirmed smooth, porous nanofibers (200-300 nm).
  • Scaffolds exhibited good water retention, moderate biodegradability, and sustained LCN release up to 72 hours.
  • Significant antibacterial and antibiofilm activity against *P. aeruginosa* and *S. aureus* was observed.
  • In vitro studies showed enhanced cell viability, adhesion, proliferation, and migration.
  • In vivo studies demonstrated accelerated infectious wound healing in diabetic rats.

Conclusions:

  • LCN-enriched PVA/PCL nanofiber scaffolds show excellent physicochemical and mechanical properties for wound healing.
  • These scaffolds possess significant antimicrobial, cytocompatible, and in vivo wound healing capabilities.
  • The developed LCN-loaded scaffolds represent a promising therapeutic strategy for multidrug-resistant infectious wounds in diabetic models.