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Assessment of photoprotection against pigmentation induced by visible light using a new in vitro method: correlation and new in vivo photoprotection factor against visible light
Assessment of photoprotection against pigmentation induced by visible light using a new in vitro method: correlation and new in vivo photoprotection factor against visible light
Thierry Passeron1,2, Luc Duteil3, Benoît Cadars4,5, Catherine Queille-Roussel3, Ingrid Giraud4, Fanny Drulhon4, Christelle Graizeau4,5, Aurélie Guyoux4
1Department of Dermatology, Nice University Hospital, Côte d’Azur University, Nice, France
2C3M, INSERM U1065, Côte d’Azur University, Nice, France
3Centre for Clinical Pharmacology Applied to Dermatology (CPCAD), L’Archet 2 Hospital, Nice, France
4NAOS Group, Research and Development Department, Aix-en-Provence, France
5NAOS Institute of Life Science, Aix-en-Provence, France
Related topics
While ultraviolet radiation is the main cause of skin pigmentation, visible light (400-700 nm) has more recently been shown to be a major contributor, in particular in melanocompetent subjects. The fact that photoprotection against visible light, in particular blue light, improves a number of hyperpigmentation disorders has led to the development of sunscreens containing specific pigments that block blue light (iron oxides and titanium dioxide). To assess the efficacy of sunscreens on visible light photoprotection, an assessment method has recently been suggested by Lim et al. based on in vivo pigmentation, leading to the calculation of the visible light photoprotection factor (VL-PF). This involves measuring changes in the ITA colorimetric parameter over several days using a chromameter. However, although in vivo methods are still the most representative of real life, in vitro methods are better suited to screening suncare formulations. The purpose of this study was to assess the correlation between in vivo and in vitro methods in assessing protection against visible light-induced pigmentation.
Initially, the in vitro photoprotective properties of 10 sunscreens (9 of which contained pigments) offering very high photoprotection (≥SPF50+) were analysed using transmission measurements in the visible spectrum. Next, a single-centre, double-blind, randomised controlled study with intra-individual comparisons on 20 healthy subjects was carried out to measure the in vivo VL-PF of these sunscreens. This VL-PF was reinterpreted as a percentage using the (1-(1/VL-PF))×100 formula and named pVL-PF (0% corresponding with an untreated exposed area and 100% with full theoretical protection against visible light, equivalent to an unexposed area). The correlation between pVL-PF and the percentage of blocked light was assessed using the coefficient of determination R, for each test area, for each wavelength from 400 to 700 nm and for each wavelength range from the 400 nm wavelength. Statistical analysis was carried out using Pearson correlation.
In vitro, the transmission spectra of tinted sunscreens showed that the best protection was achieved in high-energy visible light. In vivo, twenty subjects (13 women and 7 men) with an average age of 34.9 (18 to 49) were included in the study. The pVL-PF obtained ranged from 9.7% (for the non-tinted sunscreen) to 66.4% (for one of the tinted sunscreens). A highly significant correlation was demonstrated between the in vivo visible light protection factor and the in vitro transmission measurements. Correlations were highest at 420 nm (R²=0.9910) for distinct wavelengths, and from 400 to 469 nm (R2=0.9904) for wavelength ranges starting at 400 nm. This suggests a strong linear relationship between the in vivo pVL-PF measurement of sunscreens and the percentage of visible light blocked in vitro between 400 and 469 nm, in particular at 420 nm.
pVL-PF is a new interpretation of the original VL-PF for a more intuitive assessment from 0% to 100% of the performance on protection against visible light-induced pigmentation, making it easier to compare various formulations. This should also facilitate the understanding of dermatologists and consumers looking for a high level of photoprotection against visible light. Interestingly, the best correlation between in vivo pigmentation and in vitro transmittance was observed from 400 to 469 nm, which corresponds with the absorption spectrum of opsin-3. Melanocytes detect blue light directly by stimulating the opsin-3 receptor. In conclusion, the in vitro method using transmittance measurement from 400 to 469 nm is an appropriate predictive tool when assessing the visible light photoprotection efficacy of sunscreens, and could be used to select formulations prior to the final in vivo assessment.
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