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Published on: October 3, 2018
Singlet oxygen luminescence kinetics under PDI relevant conditions of pathogenic dermatophytes and molds
Tobias Bornhütter1, Nedaa Shamali1, Irena Saltsman2
1Department of Physics, Humboldt-Universität zu Berlin, Newtonstraße 15, 12489 Berlin, Germany.
Abstract:
A treatment of onychomycosis using the photodynamic effect would be a favorable alternative to currently used antimycotic drugs. This study should be considered as a first step towards development and control of an efficient photodynamic inactivation of onychomycosis causative pathogens. Here, we evaluate the usage of time-resolved 2D singlet oxygen luminescence detection in combination with 2D fluorescence scanning as a tool to understand the behavior of the photosensitizer when applied to fungi on Petri dishes. To investigate the interaction of photosensitizer with fungi in various concentrations and in different stages of live, a photodynamic inactivation was avoided by keeping the samples in darkness. Scans of singlet oxygen luminescence and photosensitizer fluorescence were performed over a period of 24days. Two different photosensitizer, a cationic porphyrin and cationic corrole and two fungi strains, the dermatophyte Trichophyton rubrum and the mold Scopulariopsis brevicaulis, were investigated in this study. The two-dimensional correlation of photosensitizer fluorescence and singlet oxygen luminescence revealed differences in the diffusion of both photosensitizer. Even though the singlet oxygen luminescence was quenched with increasing growth of fungi, it was found that the kinetics of singlet oxygen luminescence could be detected on Petri dishes for both photosensitizers and both fungi strains for up to seven days.
Insights
Photodynamic therapy offers a promising alternative for treating onychomycosis. This study explored photosensitizer behavior with fungi, detecting singlet oxygen luminescence for up to seven days, paving the way for effective treatments.
Area of Science:
- Photodynamic therapy
- Medical mycology
- Biophotonics
Background:
- Onychomycosis (fungal nail infection) treatment currently relies on antimycotic drugs.
- Photodynamic therapy presents a potential alternative with a different mechanism of action.
- Understanding photosensitizer-fungi interactions is crucial for developing effective photodynamic inactivation strategies.
Purpose of the Study:
- To evaluate time-resolved 2D singlet oxygen luminescence detection and 2D fluorescence scanning.
- To understand photosensitizer behavior when applied to fungi on Petri dishes.
- To investigate photosensitizer-fungi interactions in various concentrations and growth stages.
Main Methods:
- Utilized time-resolved 2D singlet oxygen luminescence detection and 2D fluorescence scanning.
- Investigated two photosensitizers (cationic porphyrin, cationic corrole) and two fungi (Trichophyton rubrum, Scopulariopsis brevicaulis).
- Monitored photosensitizer fluorescence and singlet oxygen luminescence over 24 days in darkness to avoid inactivation.
Main Results:
- Two-dimensional correlation revealed differences in photosensitizer diffusion.
- Singlet oxygen luminescence was quenched with increasing fungal growth.
- Kinetics of singlet oxygen luminescence were detectable for both photosensitizers and fungi for up to seven days.
Conclusions:
- The study provides a foundational understanding of photosensitizer-fungi interactions for photodynamic therapy.
- Time-resolved luminescence detection is a viable tool for assessing photosensitizer behavior in this context.
- Further development is needed to optimize photodynamic inactivation of onychomycosis pathogens.
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