Abstract
Photodynamic activity of tetrakis-(3-methylpyridyloxy)- and tetrakis-(4-sulfophenoxy)-phthalocyanine zinc(II) toward the gram-positive Staphylococcus aureus, the gram-negative Pseudomonas aeruginosa, and the fungi Candida albicans was studied. The drug uptake dependency with an inverse behavior to the cell density was observed. The cationic photosensitizer completely inactivated S. aureus and C. albicans, and with 4 log10 P. aeruginosa. The photoinactivation at mild experimental conditions, such as drug dose of 1.5 microM and fluence of 50 mW cm(-2) for 10 min irradiation time, was shown.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Anti-Infective Agents / chemistry
-
Anti-Infective Agents / pharmacology*
-
Candida albicans / drug effects
-
Candida albicans / pathogenicity
-
Candida albicans / radiation effects
-
Indoles / chemistry*
-
Indoles / pharmacology*
-
Isoindoles
-
Microbial Viability / drug effects
-
Microbial Viability / radiation effects
-
Molecular Structure
-
Photosensitizing Agents / chemistry*
-
Photosensitizing Agents / pharmacology*
-
Pseudomonas aeruginosa / drug effects
-
Pseudomonas aeruginosa / pathogenicity
-
Pseudomonas aeruginosa / radiation effects
-
Solubility
-
Staphylococcus aureus / drug effects
-
Staphylococcus aureus / pathogenicity
-
Staphylococcus aureus / radiation effects
-
Water / chemistry*
-
Zinc / chemistry*
Substances
-
Anti-Infective Agents
-
Indoles
-
Isoindoles
-
Photosensitizing Agents
-
Water
-
Zinc
-
phthalocyanine