Long-term moxifloxacin release from a chitosan-based antibacterial coating on polyethylene for biomedical

Helton J Wiggers1, Nathália F Sczesny1,2, Pascale Chevallier2

  • 1Laboratory for Biomaterials and Bioengineering (LBB-BPK), Associação de Ensino, Pesquisa e Extensão BIOPARK Toledo 85919-899 PR Brazil helton.wiggers@bpkedu.com.br.

RSC Advances
|January 29, 2026
PubMed

Insights

This study developed a durable antibacterial coating for medical polyethylene surfaces using moxifloxacin-loaded chitosan. The novel functionalization method ensures long-lasting protection against bacterial infections, reducing hospital-associated infections.

Area of Science:

  • Biomaterials Engineering
  • Infectious Disease Research
  • Polymer Science

Background:

  • Medical-grade polyethylene (PE) surfaces are prone to bacterial colonization and biofilm formation, contributing to hospital-associated infections (HAIs).
  • Current antibacterial coatings often suffer from limited efficacy duration and poor substrate adhesion.
  • Natural polymers offer an alternative to systemic antibiotics for preventing biofilm formation.

Purpose of the Study:

  • To develop a robust antibacterial coating for polyethylene (PE) medical devices with prolonged antimicrobial activity and enhanced adhesion.
  • To investigate a wet-chemistry functionalization strategy involving polydopamine for improved coating performance.
  • To evaluate the adhesion, drug release kinetics, and antibacterial efficacy of the developed coating.

Main Methods:

  • Polyethylene surfaces were functionalized using piranha solution and polydopamine deposition.
  • Moxifloxacin-loaded chitosan formulations were applied as coatings.
  • Surface characterization was performed using XPS to confirm chemical modifications.
  • Coating adhesion was tested in phosphate-buffered saline (PBS) over 35 days.
  • Antibiotic release profiles and antibacterial activity against *S. aureus* and *E. coli* were assessed over 160 days.

Main Results:

  • The functionalization process enhanced surface roughness and hydrophilicity, facilitating uniform polymer coating deposition.
  • XPS analysis confirmed successful surface modification with carbon oxidate species, polydopamine, and chitosan.
  • The coating demonstrated stable adhesion to the PE substrate for at least 35 days.
  • Moxifloxacin exhibited an initial burst release followed by sustained release over the study period.
  • The antibacterial coating effectively inhibited the growth of *S. aureus* and *E. coli* for up to 160 days.

Conclusions:

  • A wet-chemistry functionalization approach, including polydopamine activation, creates a strongly adhered, long-lasting antibacterial chitosan-based coating on PE.
  • This strategy provides sustained moxifloxacin release and effective inhibition of clinically relevant pathogens.
  • The developed coating represents a promising approach to reduce hospital-associated infections associated with medical devices.

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