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Role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin

The impact of sunscreen formulations on the barrier properties of human skin are often overlooked leading to formulations with components whose effects on barrier mechanical integrity are poorly understood. The aim of this study is to demonstrate the relevance of carrier selection and sunscreen phot...

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Autores principales: Berkey, Christopher, Oguchi, Nozomi, Miyazawa, Kazuyuki, Dauskardt, Reinhold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562193/
https://www.ncbi.nlm.nih.gov/pubmed/31211250
http://dx.doi.org/10.1016/j.bbrep.2019.100657
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author Berkey, Christopher
Oguchi, Nozomi
Miyazawa, Kazuyuki
Dauskardt, Reinhold
author_facet Berkey, Christopher
Oguchi, Nozomi
Miyazawa, Kazuyuki
Dauskardt, Reinhold
author_sort Berkey, Christopher
collection PubMed
description The impact of sunscreen formulations on the barrier properties of human skin are often overlooked leading to formulations with components whose effects on barrier mechanical integrity are poorly understood. The aim of this study is to demonstrate the relevance of carrier selection and sunscreen photostability when designing sunscreen formulations to protect the biomechanical barrier properties of human stratum corneum (SC) from solar ultraviolet (UV) damage. Biomechanical properties of SC samples were assayed after accelerated UVB damage through measurements of the SC's mechanical stress profile and corneocyte cohesion. A narrowband UVB (305–315 nm) lamp was used to expose SC samples to 5, 30, 125, and 265 J cm(−2) in order to magnify damage to the mechanical properties of the tissue and characterize the UV degradation dose response such that effects from smaller UV dosages can be extrapolated. Stresses in the SC decreased when treated with sunscreen components, highlighting their effect on the skin prior to UV exposure. Stresses increased with UVB exposure and in specimens treated with different sunscreens stresses varied dramatically at high UVB dosages. Specimens treated with sunscreen components without UVB exposure exhibited altered corneocyte cohesion. Both sunscreens studied prevented alteration of corneocyte cohesion by low UVB dosages, but differences in protection were observed at higher UVB dosages indicating UV degradation of one sunscreen. These results indicate the protection of individual sunscreen components vary over a range of UVB dosages, and components can even cause alteration of the biomechanical barrier properties of human SC before UV exposure. Therefore, detailed characterization of sunscreen formulation components is required to design robust protection from UV damage.
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spelling pubmed-65621932019-06-17 Role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin Berkey, Christopher Oguchi, Nozomi Miyazawa, Kazuyuki Dauskardt, Reinhold Biochem Biophys Rep Research Article The impact of sunscreen formulations on the barrier properties of human skin are often overlooked leading to formulations with components whose effects on barrier mechanical integrity are poorly understood. The aim of this study is to demonstrate the relevance of carrier selection and sunscreen photostability when designing sunscreen formulations to protect the biomechanical barrier properties of human stratum corneum (SC) from solar ultraviolet (UV) damage. Biomechanical properties of SC samples were assayed after accelerated UVB damage through measurements of the SC's mechanical stress profile and corneocyte cohesion. A narrowband UVB (305–315 nm) lamp was used to expose SC samples to 5, 30, 125, and 265 J cm(−2) in order to magnify damage to the mechanical properties of the tissue and characterize the UV degradation dose response such that effects from smaller UV dosages can be extrapolated. Stresses in the SC decreased when treated with sunscreen components, highlighting their effect on the skin prior to UV exposure. Stresses increased with UVB exposure and in specimens treated with different sunscreens stresses varied dramatically at high UVB dosages. Specimens treated with sunscreen components without UVB exposure exhibited altered corneocyte cohesion. Both sunscreens studied prevented alteration of corneocyte cohesion by low UVB dosages, but differences in protection were observed at higher UVB dosages indicating UV degradation of one sunscreen. These results indicate the protection of individual sunscreen components vary over a range of UVB dosages, and components can even cause alteration of the biomechanical barrier properties of human SC before UV exposure. Therefore, detailed characterization of sunscreen formulation components is required to design robust protection from UV damage. Elsevier 2019-06-10 /pmc/articles/PMC6562193/ /pubmed/31211250 http://dx.doi.org/10.1016/j.bbrep.2019.100657 Text en © 2019 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Berkey, Christopher
Oguchi, Nozomi
Miyazawa, Kazuyuki
Dauskardt, Reinhold
Role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin
title Role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin
title_full Role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin
title_fullStr Role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin
title_full_unstemmed Role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin
title_short Role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin
title_sort role of sunscreen formulation and photostability to protect the biomechanical barrier function of skin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562193/
https://www.ncbi.nlm.nih.gov/pubmed/31211250
http://dx.doi.org/10.1016/j.bbrep.2019.100657
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