Paper
30 December 1999 Photodynamic effect of different aluminum and zinc phthalocyanines on isolated nerve cell
Anatoly B. Uzdensky, Anna A. Zhavoronkova, Olga Yu. Dergacheva, Valentina M. Derkacheva
Author Affiliations +
Proceedings Volume 4059, Laser Use in Oncology II; (1999) https://doi.org/10.1117/12.375260
Event: Selected Papers on Laser Use in Oncology II, 1999, none, Armenia
Abstract
The photodynamic effects of sulphonated zinc (ZnPcS2, ZnPcS3 and ZnPcS4) and aluminum (AlPcS3) phthalocyanines as well as phosphonated aluminum phthalocyanine on the firing of isolated crayfish mechanoreceptor neurons were studied. After 30 min photosensitization neurons were irradiated with He-Ne laser (632.8 nm, 0.3 W/cm2) and changes in neuron firing frequency were recorded. Neuron firing was found to be very sensitive to photodynamic impact and served as a sensitive indicator of cell photodamage. The dynamics of the neuron responses to photodynamic effects included stages of firing activation and/or inhibition prior to irreversible firing abolition and depended on the photosensitizer type and concentration. The comparison of the dependencies of neuron lifetime on photosensitizer concentrations showed that the most effective photosensitizer was ZnPcS2. High photodynamic efficiencies of phthalocyanines was related with the weak dependence of photodynamic effect on sensitizer concentration indicating to the initiation about 3 secondary chain processes such as free radical membrane damage caused by photon absorption by one photosensitizer molecule.
© (1999) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Anatoly B. Uzdensky, Anna A. Zhavoronkova, Olga Yu. Dergacheva, and Valentina M. Derkacheva "Photodynamic effect of different aluminum and zinc phthalocyanines on isolated nerve cell", Proc. SPIE 4059, Laser Use in Oncology II, (30 December 1999); https://doi.org/10.1117/12.375260
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KEYWORDS
Neurons

Aluminum

Zinc

Picosecond phenomena

Cell death

Plasma

Receptors

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