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From Wikipedia, the free encyclopedia

Phototoxicity
Other namesPhotoirritation
Effect of the common rue on skin in hot weather.
SpecialtyDermatology Edit this on Wikidata

Phototoxicity, also called photoirritation, is a chemically induced skin irritation, requiring light, that does not involve the immune system.[1] It is a type of photosensitivity.[1][2]

The skin response resembles an exaggerated sunburn. The involved chemical may enter into the skin by topical administration, or it may reach the skin via systemic circulation following ingestion or parenteral administration. The chemical needs to be "photoactive," which means that when it absorbs light, the absorbed energy produces molecular changes that cause toxicity. Many synthetic compounds, including drug substances like tetracyclines or fluoroquinolones, are known to cause these effects. Surface contact with some such chemicals causes photodermatitis, and many plants cause phytophotodermatitis. Light-induced toxicity is a common phenomenon in humans; however, it also occurs in other animals.

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Transcription

Scientific background

A phototoxic substance is a chemical compound which becomes toxic when exposed to light.

Phototoxicity is a quantum chemical phenomenon. Phototoxins are molecules with a conjugated system, often an aromatic system. They have a low-lying excited state that can be reached by excitation with visible light photons. This state can undergo intersystem crossing with neighboring molecules in tissue, converting them to toxic free radicals. These rapidly attack nearby molecules, killing cells. A typical radical is singlet oxygen, produced from regular triplet oxygen. Because free radicals are highly reactive, the damage is limited to the body part illuminated.

Photosafety evaluation

Physico-chemical properties

In vitro test systems

3T3 Neutral Red Phototoxicity Test – An in vitro toxicological assessment test used to determine the cytotoxicity and photo(cyto)toxicity effect of a test article to murine fibroblasts in the presence or absence of UVA light.

"The 3T3 Neutral Red Uptake Phototoxicity Assay (3T3 NRU PT) can be utilized to identify the phototoxic effect of a test substance induced by the combination of test substance and light. The test compares the cytotoxic effect of a test substance when tested after the exposure, then tested in the absence of exposure to a non-cytotoxic dose of UVA/vis light. Cytotoxicity is expressed as a concentration-dependent reduction of the uptake of the vital dye - Neutral Red.

Substances that are phototoxic in vivo after systemic application and distribution to the skin, as well as compounds that could act as phototoxicants after topical application to the skin can be identified by the test. The reliability and relevance of the 3T3 NRU PT have been evaluated, and the test has been shown to be predictive when compared with acute phototoxicity effects in vivo in animals and humans." Taken with permission from [1]

During drug development

Several health authorities have issued related guidance documents, which need to be considered for drug development:

Phototoxicity in light microscopy

When performing microscopy on live samples, one needs to be aware that too high light dose can damage or kill the specimens and lead to experimental artefacts. This is particularly important in confocal and super-resolution microscopy.[7][8]

See also

References

  1. ^ a b Anderson, D.M.; Keith, J.; Novac, P.; Elliott, M.A., eds. (1994). Dorland's Illustrated Medical Dictionary (28th ed.). W. B. Saunders Company. ISBN 0721655777.
  2. ^ JH Epstein (1999). "Phototoxicity and photoallergy". Seminars in Cutaneous Medicine and Surgery. 18 (4): 274–284. doi:10.1016/s1085-5629(99)80026-1. PMID 10604793.
  3. ^ "Bergamot oil". Drugs.com. 2018. Retrieved 5 December 2018.
  4. ^ "Multidisciplinary Guidelines". ICH. Retrieved 2013-08-06.
  5. ^ a b "Safety Guidelines". ICH. Retrieved 2013-08-06.
  6. ^ a b "European Medicines Agency - Non-clinical: Toxicology". Ema.europa.eu. 2010-06-24. Archived from the original on 2013-01-19. Retrieved 2013-08-06.
  7. ^ Icha, Jaroslav; Weber, Michael; Waters, Jennifer C.; Norden, Caren (2017). "Phototoxicity in live fluorescence microscopy, and how to avoid it". BioEssays. 39 (8): 1700003. doi:10.1002/bies.201700003. hdl:21.11116/0000-0002-8C94-9. ISSN 1521-1878. PMID 28749075. S2CID 19974817.
  8. ^ Laissue, P. Philippe; Alghamdi, Rana A.; Tomancak, Pavel; Reynaud, Emmanuel G.; Shroff, Hari (July 2017). "Assessing phototoxicity in live fluorescence imaging". Nature Methods. 14 (7): 657–661. doi:10.1038/nmeth.4344. hdl:21.11116/0000-0002-8B80-0. ISSN 1548-7105. PMID 28661494. S2CID 6844352.

External links

This page was last edited on 8 March 2024, at 09:55
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