Photodynamic effects of 31 different phthalocyanines on a human keratinocyte cell line
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
23790830
DOI
10.1016/j.chemosphere.2013.05.032
PII: S0045-6535(13)00767-4
Knihovny.cz E-resources
- Keywords
- HaCaT, Keratinocyte cell lines, Phototoxicity, Phthalocyanines, Reactive oxygen species (ROS), Singlet oxygen,
- MeSH
- Cell Line MeSH
- Photosensitizing Agents toxicity MeSH
- Indoles toxicity MeSH
- Isoindoles MeSH
- Keratinocytes drug effects metabolism MeSH
- Humans MeSH
- Singlet Oxygen metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Photosensitizing Agents MeSH
- Indoles MeSH
- Isoindoles MeSH
- phthalocyanine MeSH Browser
- Singlet Oxygen MeSH
Phthalocyanines (Pcs, colored macromolecular compounds with the ability to generate singlet oxygen) represent a promising group of photosensitizers due to their intense absorption in the red and UV portion of the spectrum which leads to their excitation. In order to characterize possible toxic effects associated with eventual practical use and application of these chemicals, we employed an in vitro cell culture model to evaluate cytotoxic effects of 31 different phthalocyanines using neutral red uptake assay. An immortalized human keratinocyte cell line HaCaT was exposed to the tested chemicals for 2 or 24h, either with or without illumination in the last 60 min of the exposure period. After 2- or 24-h exposure without illumination, no cytotoxic effects or weak cytotoxic effects were induced by any Pc under the study and EC50 values could not be obtained within the tested concentration ranges (1.25-20 mg L(-1) or 0.625-10 mg L(-1)). On the other hand, exposure to phthalocyanines under illumination induced a significant cytotoxic effect. The most pronounced cytotoxicity was elicited by Pcs previously shown to have high positive charge densities at peripheral parts of substituent groups, which is most likely the factor responsible for the binding of Pc to negatively charged membranes on the cell surface and thus guaranteeing the tight connection necessary for the singlet oxygen attack on the cell surface.
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