PubMed · 14419900
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B MAGNUSSON. 1959-11-20. [Photodermatitis].. https://pubmed.ncbi.nlm.nih.gov/14419900/
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The sun is essential for life. Yet, sunlight can also be a source of such deleterious effects as sunburn, and suntanning, as well as premalignant and malignant lesions. These may all occur in individuals with normal responses to sunlight. In addition, there exist a variety of 'abnormal' photosensitivity responses to sunlight that may result from either endogenous imbalances (e.g. the porphyrias) or from added exogenous factors (e.g. drug photosensitivity). The 'normal' responses to sunlight, by and large, are produced preferentially by UVB (290-320 nm), with minor contribution by UVA (320-400 nm) wavelengths. In contrast, the 'abnormal' photosensitivity responses are, for the most part, elicited predominantly by long UVA and, in some cases, visible light. In the last 20 years or so, considerable attention has been paid to the use of fabrics as photoprotective materials. The vast majority of work in this area has been concerned with fabric protection against sunburn. In addition to in vivo measurement of fabric SPF, in vitro evaluation of fabric UPF has been carried out in numerous laboratories around the world. The UPF is estimated from the wavelength-dependent transmission of the fabric, the solar UV spectrum and the erythemal action spectrum over the wavelength region 290-400 nm. Depending on the fabric, UPF values range from 2 to several thousand. More recently, it has become clear that such environmental influences as laundering, solarization, humidity, wetting and degree of stretching may play a major role in fabric protection. Protection also may be altered by addition of dyes, UV absorbers and fluorescent whitening agents. To date, there have been relatively few studies of fabric protection for endpoints other than sunburn erythema. Yet, many fabrics that provide good protection against sunburn may provide inadequate protection against photosensitization by intrinsic or extrinsic absorbing molecules or against (pre)malignant lesions. Future work should explicity address the efficacy of protective fabrics against photosensitivity diseases that are activated by long UVA or visible wavelengths.
Investigators using models to determine the phototoxic effects of sunlight on polycyclic aromatic hydrocarbons (PAHs) have invoked the excited states of the molecule as important in elucidating the mechanism of these reactions. Energies of actual excited states were calculated for ten PAHs by several ab initio methods. The main method used for these calculations was the Configuration Interaction approach, modeling excited states as combinations of single substitutions out of the Hartree-Fock ground state. These calculations correlate well with both experimentally measured singlet and triplet state energies and also previous HOMO-LUMO gap energies that approximate the singlet state energies. The excited state calculations then correlate well with general models of photo-induced toxicity based for the PAHs.
BACKGROUND/PURPOSE: Drug-induced phototoxicity is a non-immunological inflammatory skin reaction, caused by concurrent topical or systemic exposure to a specific molecule and ultraviolet radiation. Most of phototoxic compounds absorb energy particularly from UVA light leading to activated derivatives, which can induce cellular damage. This type of adverse cutaneous response can be reproduced, in vitro, using human skin models. In this study, we investigated the ability of human reconstituted epidermis Episkin to assess skin phototoxicity of weak phototoxic compounds such as 6-methylcoumarin and ofloxacin, compared to a strong one, chlorpromazine, and two negative controls (sodium dodecyl sulphate (SDS), sulisobenzone). METHODS: : After 1 h incubation with five test concentrations of each chemical compound, epidermis was then exposed or not to UVA at a non-cytotoxic dose (50 J/cm2). 18 h after UVA exposure, cellular damage was evaluated measuring cytotoxicity by MTT conversion test; in addition, pro-inflammatory mediator IL-1alpha release was also investigated. RESULTS: Topical pretreatment of Episkin, with weak phototoxic compounds induced, after UVA exposure, a dose-dependent decrease in cell viability, in concordance with an increasing IL-1alpha release. Moreover, compared to chlorpromazine, the lower IL-1alpha release observed with 6-methylcoumarin and ofloxacin could be linked to their weak phototoxic potential. CONCLUSION: Human reconstituted epidermis Episkin can be useful to study in vitro the onset of cutaneous phototoxic reactions and particularly to identify weak phototoxic compounds.