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Published on: March 1, 2013
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.
Abstract:
Medical-grade polyethylene (PE) surfaces are highly susceptible to bacterial colonization and biofilm formation, leading to hospital-associated infections (HAIs). Antibacterial coatings based on natural polymers offer a promising strategy to prevent biofilm establishment while mitigating systemic antibiotic use. However, there are some bottlenecks such as the limited duration of antimicrobial activity and the poor adhesion of the coating to the substrate. In this study, an antibacterial coating with prolonged activity was developed, based on prior work with moxifloxacin-loaded chitosan films. To promote coating adhesion, an approach consisting in wet-chemistry functionalization was studied. PE was treated with piranha solution followed by polydopamine deposition and coated with the moxifloxacin-loaded chitosan formulation. The coatings exhibited uniform coverage; piranha treatment increased roughness and enhanced hydrophilicity, allowing polymer deposition. XPS confirmed successful carbon oxidate species after piranha treatment, and enabled the identification of polydopamine and chitosan, observed by oxygen and nitrogen enrichment. Coating adhesion strength remained stable over 35 days in PBS. Antibiotic release profiles of film and coating were similar, displaying an initial burst (first 10 days) followed by sustained release of moxifloxacin. Antibacterial assay confirmed activity of the coating against S. aureus and E. coli for up to 160 days. Therefore, a wet-chemistry functionalization approach followed by polydopamine activation yields a strongly adhered antibacterial chitosan-based coating on PE that provides long-term moxifloxacin release and effective inhibition of clinically relevant pathogens. This proof-of-concept study represents a straightforward strategy to produce antimicrobial coatings with prolonged activity to reduce HAIs in medical devices.
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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