Photodynamic Action of Tri-meso (N-methylpyridyl), meso (N-tetradecyl-pyridyl) Porphine on Staphylococcus Epidermidis Biofilms Grown on Ti6Al4V Alloy

Author:

Saino Enrica12,Sbarra Maria S.12,Arciola Carla Renata34,Scavone Mariangela1,Bloise Nora1,Nikolov Peter5,Ricchelli Fernanda6,Visai Livia12

Affiliation:

1. Department of Biochemistry, University of Pavia, Pavia - Italy

2. Center for Tissue Engineering (CIT), University of Pavia, Pavia - Italy

3. Research Unit on Implant Infections, Rizzoli Orthopedic Institute, Bologna - Italy

4. Experimental Pathology Department, University of Bologna, Bologna - Italy

5. Bulgarian Academy of Sciences, Institute of Organic Chemistry, Sofia - Bulgary

6. CNR, Institute of Biomedical Technology at the Department of Biology, University of Padova, Padova - Italy

Abstract

Staphylococcus epidermidis is a leading cause of nosocomial infections, and its virulence is attributable to formation of biofilm, especially on implanted devices. Photodynamic treatment (PDT) has been actively investigated for the eradication of bacterial biofilm growing on dental plaques and oral implants. In this study, we used Tri-meso (N-methyl-pyridyl), meso (N-tetradecyl-pyridyl) porphine (C14) for inactivation of two structurally distinct S. epidermidis biofilms grown on Ti6Al4V alloy and compared its photosensitizing efficiency with that of the parent molecule, tetra-substituted N-methylpyridyl-porphine (C1). A more significant reduction in bacterial survival was observed when both bacterial biofilms were exposed to a lower dose of C14, and simultaneously to visible light in comparison with C1. The different responses of both staphylococcal biofilms to C1- or C14-treatment appeared to depend on photosensitizer endocellular concentration. C14 bound to both biofilms to a greater extent than C1. Moreover, C14 penetrates deeper into the bacterial membranes, as determined by fluorescence quenching experiments with methylviologen, allowing for better bacterial killing photoefficiency. Confocal laser scanning microscope (CLSM) analysis indicated damage to bacterial cell membranes in both photodynamically treated biofilms, while disruption of PDT-treated biofilm was confirmed by scanning electron microscopy (SEM). In summary, C14 may be a potential photosensitizer for the inactivation of staphylococcal biofilms for many device-related infections which are accessible to visible light.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials,General Medicine,Medicine (miscellaneous),Bioengineering

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