Paper
17 July 2009 Photodynamic inactivation of the models Mycobacterium phlei and Mycobacterium smegmatis in vitro
R. Bruce-Micah, U. Gamm, D. Hüttenberger, J. Cullum, H.-J. Foth
Author Affiliations +
Abstract
Photodynamic inactivation (PDI) of bacterial strains presents an attractive potential alternative to antibiotic therapies. Success is dependent on the effective accumulation in bacterial cells of photochemical substances called photosensitizers, which are usually porphyrins or their derivatives. The kinetics of porphyrin synthesis after treatment with the precursor ALA and the accumulation of the Chlorin e6 and the following illumination were studied. The goal was to estimate effectivity of the destructive power of these PS in vitro in respect of the physiological states of Mycobacteria. So the present results examine the cell destruction by PDI using ALA-induced Porphyrins and Chlorin e6 accumulated in Mycobacterium phlei and Mycobacterium smegmatis, which serve as models for the important pathogens Mycobacterium tuberculosis, Mycobacterium leprae and Mycobacterium bovis. We could show that both Mycobacterium after ALA and Chlorin e6 application were killed by illumination with light of about 662 nm. A reduction of about 97% could be reached by using a lightdose of 70 mW/cm2.
© (2009) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
R. Bruce-Micah, U. Gamm, D. Hüttenberger, J. Cullum, and H.-J. Foth "Photodynamic inactivation of the models Mycobacterium phlei and Mycobacterium smegmatis in vitro", Proc. SPIE 7373, Therapeutic Laser Applications and Laser-Tissue Interactions IV, 73731L (17 July 2009); https://doi.org/10.1117/12.831872
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KEYWORDS
Bacteria

Oxygen

Picosecond phenomena

Luminescence

Photodynamic therapy

In vitro testing

Pathogens

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