Antimicrobial Activity of Poly(ester urea) Electrospun Fibers Loaded with Bacteriophages

• Published in: Fibers Vol. 6; no. 2; p. 33
• Main Authors: Díaz, Angélica, Del Valle, Luis, Rodrigo, Noel, Casas, María, Chumburidze, George, Katsarava, Ramaz, Puiggalí, Jordi
• Format: Journal Article Publication
• Language: English
• Published: Basel MDPI AG 01.06.2018
• Subjects: Antibiotics; Antimicrobial agents; Bacteria; Bacterial infections; bactericides; Bacteriophages; Bacteriòfags; Biocompatibility; Biodegradable materials; Biomedical materials; Calcium carbonate; Cellulose; E coli; Electrospinning; Enginyeria química; Infections; Leucine; Materials biomèdics; Molecular weight; Morphology; Mortality; Nanofibers; Nanotechnology; Particle size; Phages; poly(ester urea)s; Polyethylene glycol; Polymers; Polyvinyl alcohol; Polímers; scaffolds; Solvents; Ureas; Water soluble polymers; Àrees temàtiques de la UPC; Spain
• ISSN: 2079-6439; 2079-6439
• DOI: 10.3390/fib6020033

The capacity to load bacteriophages into electrospun nanofibers of two representative biocompatible polymers has been evaluated, paying special attention to the possibility of preserving their antibacterial activity. Specifically, the work involves the following steps: (a) Evaluation of the effect of the applied electrical field on the phage activity; (b) evaluation of the activity when a lyophilization process could be avoided by using water soluble polymers (e.g., poly(ethylene glycol); (c) evaluation of the activity when dissolution of the polymer requires an organic solvent and lyophilization is theoretically necessary. In this case, a poly(ester urea) (PEU) derived from the natural L-leucine amino acid has been considered. Adsorption of commercial bacteriophage preparations into calcium carbonate particles was demonstrated to be a promising methodology to avoid lyophilization and keep the initial bactericide activity at a maximum. Phagestaph and Fersis bacteriophage commercial preparations have been selected for this study due to their specific activity against Staphylococci (e.g., S. aureus) and Streptococci (e.g., S. pyogenes) bacteria. Adhesion and proliferation assays using epithelial cells demonstrated the biocompatibility of both unloaded and bacteriophage-loaded PEU scaffolds, although some slight differences were observed depending on the type of bacteriophage and the selected preparation methodology.