1
Unité Mixte de Recherche (UMR) S949, Inserm, Strasbourg 67000, France
2
Etablissement Français du Sang-Alsace (EFS-Alsace), Strasbourg 67000, France
3
Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg 67000, France
4
Université de Strasbourg, Strasbourg 67000, France
5
Materials Engineering Center, UdR INSTM, University of Perugia, Terni 05100, Italy
6
Department of Molecular Medicine, INSTM UdR of Pavia, Biochemistry Unit, “A Castellani”, Viale Taramelli, 3/b-27100 Pavia, Center for Health Technologies (C.H.T.), University of Pavia, Pavia 27100, Italy
7
Department of Public Health, Experimental Medicine and Forensics, University of Pavia, Pavia 27100, Italy
8
Department of Occupational Medicine, Toxicology and Environmental Risks, S. Maugeri Foundation, IRCCS Pavia 27100, Italy
9
Research Unit on Implant Infections, Rizzoli Orthopaedic Institute, and DIMES, University of Bologna, Via di Barbiano 1/10-40136, Bologna, Italy
Abstract
The purpose of this study was to investigate the antimicrobial properties of multifunctional nanocomposites based on poly(
dl-Lactide-co-Glycolide) (PLGA) and increasing concentration of silver (Ag) nanoparticles and their effects on cell viability for biomedical applications. PLGA nanocomposite films, produced by solvent casting
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The purpose of this study was to investigate the antimicrobial properties of multifunctional nanocomposites based on poly(
dl-Lactide-co-Glycolide) (PLGA) and increasing concentration of silver (Ag) nanoparticles and their effects on cell viability for biomedical applications. PLGA nanocomposite films, produced by solvent casting with 1 wt%, 3 wt% and 7 wt% of Ag nanoparticles were investigated and surface properties were characterized by atomic force microscopy and contact angle measurements. Antibacterial tests were performed using an
Escherichia coli RB and
Staphylococcus aureus 8325-4 strains. The cell viability and morphology were performed with a murine fibroblast cell line (L929) and a human osteosarcoma cell line (SAOS-2) by cell viability assay and electron microscopy observations. Matrix protein secretion and deposition were also quantified by enzyme-linked immunosorbent assay (ELISA). The results suggest that the PLGA film morphology can be modified introducing a small percentage of silver nanoparticles, which induce the onset of porous round-like microstructures and also affect the wettability. The PLGA/Ag films having silver nanoparticles of more than 3 wt% showed antibacterial effects against
E. coli and
S. aureus. Furthermore, silver-containing PLGA films displayed also a good cytocompatibility when assayed with L929 and SAOS-2 cells; indicating the PLGA/3Ag nanocomposite film as a promising candidate for tissue engineering applications.
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