Determination of Antibacterial Activity of Film Coatings against Four Clinically Relevant Bacterial Strains
Natalia Scilletta,
Magdalena Pezzoni,
Martin Desimone,
Galo Soler-Illia,
Martin Bellino,
Paolo Catalano
Affiliations
Natalia Scilletta
Departamento de Micro y Nanotecnología, Instituto de Nanociencia y Nanotecnología-Comisión Nacional de Energía Atómica y Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. General Paz 1499, B1650KNA San Martín, Argentina
Magdalena Pezzoni
Departamento de Radiobiología, Comisión Nacional de Energía Atómica, Av. General Paz 1499, B1650KNA San Martín, Argentina y Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)
Martin Desimone
Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Química y Metabolismo del Fármaco (IQUIMEFA), Facultad de Farmacia y Bioquímica. Junín 956, Piso 3° (1113), Buenos Aires, Argentina
Galo Soler-Illia
Instituto de Nanosistemas, Universidad Nacional de San Martín, Av. 25 de Mayo 1021, 1650 San Martín, Argentina
Martin Bellino
Departamento de Micro y Nanotecnología, Instituto de Nanociencia y Nanotecnología-Comisión Nacional de Energía Atómica y Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. General Paz 1499, B1650KNA San Martín, Argentina
Paolo Catalano
Departamento de Micro y Nanotecnología, Instituto de Nanociencia y Nanotecnología-Comisión Nacional de Energía Atómica y Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. General Paz 1499, B1650KNA San Martín, ArgentinaUniversidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Junín 956, Piso 3° (1113), Buenos Aires, Argentina
Antibacterial coatings have currently gained great importance in biomedical technology investigations. Because of the spatial arrangement of the film coatings, evaluation of antibacterial activity presents a new challenge regarding traditional bacterial counting methods. In this protocol, four clinically relevant pathogens, Salmonella typhimurium, Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus were incubated on titania mesostructured thin film coatings for 24 h. Then, cell viability was studied considering three methods: counting of the number of colony forming units (CFU), live/dead staining, and quantification of extracellular DNA in suspension. Firstly, bacterial count was determined by the standard plate-count technique. Secondly, bacteria membrane integrity was evaluated by utilization of two fluorescent dyes, which allow distinction between live (membrane intact) and dead (membrane disrupted) bacteria. Lastly, extracellular DNA was quantified by spectrophotometry. In this manner, the three aforementioned techniques enabled the study of bacterial viability by qualitative and quantitative analyses.