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Photodynamic effect of protoporphyrin diarginate (PPArg2) on methicillin-resistant Staphylococcus aureus and human dermal fibroblasts.

Abstract
The worldwide rise in the antibiotic resistance of bacteria forces the development of alternative antimicrobial treatments. A potential approach is photodynamic inactivation (PDI). The aim of the present study was to determine the phototoxicity of protoporphyrin diarginate (PPArg(2)) against methicillin-resistant Staphylococcus aureus and human dermal fibroblasts. Different concentrations (0 to 20 microM) of PPArg(2) and light dose of 6 J cm(-2) were tested. Cell viability was evaluated using the methylthiazoletetrazolium (MTT) assay. Incubation with 10 microM followed by illumination yielded a 3.6 log(10)-unit reduction in the viable count for Staphylococcus aureus. At the same experimental conditions, only 22.5% of the fibroblasts were photoinactivated. Protoporphyrin diarginate at concentrations up to 20 microM demonstrated no toxicity towards S. aureus or fibroblasts when not irradiated. These results suggest that the protoporphyrin diarginate exerts a high bactericidal effect against methicillin-resistant S. aureus strain without harming eukaryotic cells.
AuthorsMariusz Grinholc, Anna Kawiak, Julianna Kurlenda, Alfreda Graczyk, Krzysztof P Bielawski
JournalActa biochimica Polonica (Acta Biochim Pol) Vol. 55 Issue 1 Pg. 85-90 ( 2008) ISSN: 0001-527X [Print] Poland
PMID18217106 (Publication Type: Journal Article)
Chemical References
  • Photosensitizing Agents
  • Protoporphyrins
  • Tetrazolium Salts
  • Thiazoles
  • Arginine
  • thiazolyl blue
  • Methicillin
Topics
  • Arginine (analogs & derivatives, pharmacology)
  • Dermis (cytology)
  • Dose-Response Relationship, Drug
  • Drug Resistance, Bacterial
  • Fibroblasts (cytology, metabolism)
  • Humans
  • Light
  • Methicillin (pharmacology)
  • Methicillin Resistance
  • Models, Biological
  • Photochemistry (methods)
  • Photosensitizing Agents (pharmacology)
  • Protoporphyrins (pharmacology)
  • Skin (cytology, metabolism)
  • Staphylococcus aureus (metabolism)
  • Tetrazolium Salts (pharmacology)
  • Thiazoles (pharmacology)

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