A Spectrophotometric Method to Determine Minimal Erythema Dose for Ultraviolet Radiation in Human Skin

Background/Objectives: Ultraviolet radiation (UVR) induces oxidative stress in the skin by generating reactive oxygen species (ROS), which can lead to inflammatory conditions including erythema (a sign of sunburn). This clinical study aims to develop an instrumental evaluation method to determine the minimal erythema dose (MED) for UVR. Methods: Fourteen human subjects aged 27 to 57 years (48.93 ± 8.54) participated in this study. Six subsites were designated on the test skin site of each subject and irradiated with UVR at different doses. The examiner visually assessed erythema, determining the 'visual MED'. Additionally, the a* value (a chrominance parameter presenting greenness to redness) was measured using a spectrophotometer as an indicator of erythema. The a* values of the UVR-irradiated subsites were compared to the non-irradiated control value, and the differences were referred to as Δa*. The Δa* value of the subsites irradiated with UVR at the 'visual MED' was referred to as the Δa*_VMED for each subject. The mean of the Δa*_VMED values of all subjects was chosen as a criterion value for the 'instrumental MED'. The 'instrumental MED' was defined as the lowest dose of UVR that causes an Δa* value equivalent to the criterion value. The 'visual MED' and 'instrumental MED' values of all subjects were subjected to correlation analysis. Results: The mean of the Δa*_VMED values of all subjects was 1.88 ± 0.8. The means of the 'visual MED' and 'instrumental MED' values (in J m^-2 unit) of all subjects were 300.14 ± 84.16 and 303.29 ± 77.99, respectively. In Pearson correlation analysis, the 'instrumental MED' and 'visual MED' values had a very strong positive correlation with each other (r = 0.864, p = 0.000). Conclusions: This study suggests that the instrumental evaluation method of MED based on the spectrophotometric measurement of the a* values can complement or replace the visual evaluation method and that this method will be useful in monitoring skin tolerance to oxidative stress affected by prooxidant factors and defensive factors.