New Methodology to Evaluate Sunscreens Under Outdoor Conditions: A Double-Blind, Randomized Intra-Individual Clinical Study of a Water-Based Broad-Spectrum SPF50+Versus SPF15 (P3) and SPF50+

被引:6
|
作者
Granger, Corinne [1 ]
Krutmann, Jean [2 ]
Bustos, Javier [1 ]
Sola, Yolanda [3 ]
Hosenally, Muzzammil [4 ,5 ]
Trullas, Carles [1 ]
Andres, Philippe [6 ]
Passeron, Thierry [7 ,8 ]
机构
[1] Isdin, Innovat & Dev, Barcelona, Spain
[2] IUF Leibniz Res Inst Environm Med, Dusseldorf, Germany
[3] Univ Barcelona, Meteorol Grp, Dept Appl Phys, Marti & Franques 1, E-08028 Barcelona, Spain
[4] Univ Mauritius, Dept Econ & Stat, Reduit, Mauritius
[5] Ctr Int Dev Pharmaceut, Phoenix, Mauritius
[6] Clipeum Pharma, Peymeinade, France
[7] Univ Cotr dAzur, Ctr Hosp Univ Nice, Dept Dermatol, Nice, France
[8] Inserm C3M U1065, Nice, France
关键词
Outdoor; SPF; Sun protection; Sunburn; SPLIT-FACE; RADIATION; BIOASSAY; EFFICACY; SUNBURN; LIGHT;
D O I
10.1007/s13555-019-00315-4
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Introduction This study explored a new method to test sunscreens in outdoor conditions (very high to extreme ultraviolet [UV] radiation) approximating real-life solar exposure while maintaining scientific standards and acceptable conditions, and assessed the efficacy of a water-based sun-protection factor (SPF) 50+ versus a reference SPF15 and two comparator SPF50+ products. Methods Thirty-five subjects underwent testing in summertime Mauritius. In each subject, five test areas were marked on the back. One area was left unprotected, and four sunscreens were applied to the others: investigational product (IP), SPF15 (ISO 24444:2010 reference standard P3), and two marketed SPF50+ controls. Subjects spent 1-2 h (depending on skin type) in the sun. After 24 h, erythema was assessed by clinical scoring (0-5) and colorimetry (a*, L*, and ITA). Secondary endpoints were correlation between clinical and colorimetry assessment, product tolerability, and total UV radiation received. Results All subjects were exposed to a very high UV index (>= 8) and 30/35 were exposed to an extreme UV index (>= 11). The IP showed statistically significant differences in clinical erythema scoring compared with unprotected skin and SPF15, but not with SPF50+ controls. On colorimetry, differences in a* (redness) and L* (lightness) reached statistical significance for the IP vs SPF15 but not vs SPF50+ controls. Clinical and instrumental erythema assessment correlated strongly (Spearman's rho 0.663). No tolerability issues were reported. Conclusion This exploratory study confirmed the ability of this outdoor model to discriminate sunscreens with different SPF using clinical evaluation as an objective measure. The water-based sunscreen maintained its efficacy in outdoor conditions of very high to extreme UV radiation: it was superior to SPF15 and comparable to SPF50+ controls in preventing erythema. The method used represents an option for sunscreen efficacy comparison outside of the laboratory. Funding Isdin.
引用
收藏
页码:589 / 599
页数:11
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    Corinne Granger
    Jean Krutmann
    Javier Bustos
    Yolanda Sola
    Muzzammil Hosenally
    Carles Trullàs
    Philippe Andres
    Thierry Passeron
    Dermatology and Therapy, 2019, 9 : 589 - 599
  • [2] Outdoor testing of the photoprotection provided by a new water-based broad-spectrum SPF50+ sunscreen product: two double-blind, split-face, randomized controlled studies in healthy adults
    Granger, Corinne
    Sola, Yolanda
    Gilaberte, Yolanda
    Trullas, Caries
    CLINICAL COSMETIC AND INVESTIGATIONAL DERMATOLOGY, 2019, 12 : 461 - 467