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Comparison of UVA Protection Factor Measurement Protocols.
Kamand Hedayat1, Saman Ahmad Nasrollahi1,2, Alireza Firooz1,2
1Center for Research and Training in Skin Diseases and Leprosy (CRTSDL), Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Clinical, Cosmetic and Investigational Dermatology
|June 18, 2020
Summary
UVA rays contribute to skin aging and cancer. This review compares UVA-PF measurement methods, finding the in vivo persistent pigment darkening (PPD) method most suitable due to in vitro test condition variability.
Area of Science:
- Dermatology
- Photobiology
- Cosmetic Science
Background:
- UVA radiation (320-400nm) is increasingly recognized for its role in skin aging and potential to cause cancerous keratinocyte cells.
- Effective sunscreen formulation requires robust protection against both UVB and UVA rays.
- The UVA Protective Factor (UVA-PF) is a critical metric for assessing sunscreen efficacy against UVA radiation.
Purpose of the Study:
- To comprehensively review and compare existing protocols for measuring UVA-PF.
- To identify the most beneficial and reliable method for UVA-PF assessment.
Main Methods:
- Evaluation of four key standards: ISO 24443, CEN 2006, FDA 2007, and FDA 2011.
- Analysis of both in vivo and in vitro measurement techniques.
- Comparison based on critical wavelength, persistent pigment darkening (PPD), and modified Diffey fraction.
Main Results:
- In vivo methods utilizing the PPD approach (CEN 2006, FDA 2007) are highlighted.
- In vitro methods employ critical wavelengths (CEN, FDA 2011) or modified Diffey fraction (FDA 2007).
- ISO 24443 aligns UVA-PF measurement with the PPD method.
Conclusions:
- In vitro UVA-PF measurement methods exhibit variability due to differing test conditions, impacting reproducibility.
- The in vivo PPD method is identified as a more reliable and suitable option for accurate UVA-PF determination.
- Further development towards an integrated standard for UVA-PF measurement is recommended.
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