CARCINOGENIC POTENTIAL OF FLUORESCENT UV TANNING SOURCES CAN BE ESTIMATED USING THE CIE ERYTHEMA ACTION SPECTRUM

Citation
N. Bechthomsen et Hc. Wulf, CARCINOGENIC POTENTIAL OF FLUORESCENT UV TANNING SOURCES CAN BE ESTIMATED USING THE CIE ERYTHEMA ACTION SPECTRUM, International journal of radiation biology, 64(4), 1993, pp. 445-450
Citations number
14
Categorie Soggetti
Radiology,Nuclear Medicine & Medical Imaging","Nuclear Sciences & Tecnology
ISSN journal
09553002
Volume
64
Issue
4
Year of publication
1993
Pages
445 - 450
Database
ISI
SICI code
0955-3002(1993)64:4<445:CPOFUT>2.0.ZU;2-B
Abstract
In legislation the CIE human erythema action spectrum is used to asses s the risk of UV radiation appliances for household use. The most popu lar type of UV radiation source for private use is the low pressure 'U VA' radiation source, which mainly emits in the UVA area, but also has some emission in the UVB area. Recently reports have raised doubt whe ther the CIE erythema action spectrum is a good approximation for the carcinogenic risk. Therefore, it was investigated whether the carcinog enic potential of differing UV tanning sources, which mainly emit in t he UVA area, could be assessed by using the CIE erythema spectrum. Two groups of lightly pigmented C3H/Tif mice were initially exposed to br oad spectrum UV radiation with a high output of UVB (UVB emission 16.7 %) during 84 days, in a daily dose of 4.67 Basic minimal erythema dose s (Basic-MED). Subsequently, one group was exposed to Bellarium-S SA-1 -12 (UVB emission 6.9%), the other to Philips TL 09R (UVB emission 2.2 %), in a daily dose of 1 Basic-MED. The time to occurence of seven tum our end-points was almost identical in the two groups, p > 0.4. To obt ain further information on the relationship between the daily dose of common UV tanning sources measured in Basic-MED and tumour development , we combined the result of this experiment with the results of two ot hers. There existed a negative correlation between the daily exposure dose measured in Basic-MED and the tumour induction time, p less-than- or-equal-to 0.05. This inverse relationship was observed both when the UV tanning sources were administered with or without a prior exposure to broad spectrum UV irradiation. Our results indicate that the carci nogenic risk of UV tanning sources in the hairless C3H/Tif mouse can b e estimated by the CIE erythema action spectrum.