Cargando…

Design, synthesis and characterization of linear unnatural amino acids for skin moisturization

OBJECTIVES: This work aimed to design, synthesize and characterize replacement natural moisturizing factor (NMF) composed of modified hygroscopic linear amino acids to pre‐empt or repair skin barrier dysfunction. METHODS: Following synthesis and characterization, thermo‐gravimetric analysis and quan...

Descripción completa

Detalles Bibliográficos
Autores principales: Arezki, N. R., Williams, A. C., Cobb, A. J. A., Brown, M. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244679/
https://www.ncbi.nlm.nih.gov/pubmed/27380298
http://dx.doi.org/10.1111/ics.12351
_version_ 1782496737434271744
author Arezki, N. R.
Williams, A. C.
Cobb, A. J. A.
Brown, M. B.
author_facet Arezki, N. R.
Williams, A. C.
Cobb, A. J. A.
Brown, M. B.
author_sort Arezki, N. R.
collection PubMed
description OBJECTIVES: This work aimed to design, synthesize and characterize replacement natural moisturizing factor (NMF) composed of modified hygroscopic linear amino acids to pre‐empt or repair skin barrier dysfunction. METHODS: Following synthesis and characterization, thermo‐gravimetric analysis and quantum mechanics molecular modelling quantified and depicted water binding to the new compounds. Deliquescence relative humidity demonstrated the water‐scavenging ability of the compounds, whereas snake skin moisturizing studies showed they increased water uptake into snake skin. RESULTS: From thermal analysis, N‐hydroxyglycine showed greatest water‐holding capacity followed by N‐hydroxyserine, l‐homoserine and α‐hydroxyglycine; coupled with quantum mechanics molecular modelling, between 8 and 12 molecules of water could associate with each molecule of either N‐hydroxyglycine, N‐hydroxyserine or l‐homoserine. All of our modified amino acids were efficacious and induced similar or greater water uptake compared with the established moisturizing compounds hyaluronic acid, glycerine and urea in snake skin. Incorporated at 10% in Oilatum, N‐hydroxyserine induced >200% greater moisture uptake into dry snake skin compared to treatment with water alone, with efficacy related to the molecule structure and ability to bind to 12 water molecules. Oilatum cream spiked with all our unnatural amino acid hydrotropes increased water uptake into snake skin compared with Oilatum alone. The compound series was designed to elucidate some structure – efficacy relationships. Amino acid chirality did not affect the water‐holding capacity but did affect uptake into skin. Compounds with high melting points and bond energies tended to decrease water‐holding capacity. With isosteric replacement, the more electronegative atoms gave greater water‐holding capacities. CONCLUSIONS: This work demonstrates the potential of unnatural amino acid hydrotropes as skin moisturizers and has developed some predictive ‘rules’ for further design and refinement of chemical structures.
format Online
Article
Text
id pubmed-5244679
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-52446792017-01-25 Design, synthesis and characterization of linear unnatural amino acids for skin moisturization Arezki, N. R. Williams, A. C. Cobb, A. J. A. Brown, M. B. Int J Cosmet Sci Original Articles OBJECTIVES: This work aimed to design, synthesize and characterize replacement natural moisturizing factor (NMF) composed of modified hygroscopic linear amino acids to pre‐empt or repair skin barrier dysfunction. METHODS: Following synthesis and characterization, thermo‐gravimetric analysis and quantum mechanics molecular modelling quantified and depicted water binding to the new compounds. Deliquescence relative humidity demonstrated the water‐scavenging ability of the compounds, whereas snake skin moisturizing studies showed they increased water uptake into snake skin. RESULTS: From thermal analysis, N‐hydroxyglycine showed greatest water‐holding capacity followed by N‐hydroxyserine, l‐homoserine and α‐hydroxyglycine; coupled with quantum mechanics molecular modelling, between 8 and 12 molecules of water could associate with each molecule of either N‐hydroxyglycine, N‐hydroxyserine or l‐homoserine. All of our modified amino acids were efficacious and induced similar or greater water uptake compared with the established moisturizing compounds hyaluronic acid, glycerine and urea in snake skin. Incorporated at 10% in Oilatum, N‐hydroxyserine induced >200% greater moisture uptake into dry snake skin compared to treatment with water alone, with efficacy related to the molecule structure and ability to bind to 12 water molecules. Oilatum cream spiked with all our unnatural amino acid hydrotropes increased water uptake into snake skin compared with Oilatum alone. The compound series was designed to elucidate some structure – efficacy relationships. Amino acid chirality did not affect the water‐holding capacity but did affect uptake into skin. Compounds with high melting points and bond energies tended to decrease water‐holding capacity. With isosteric replacement, the more electronegative atoms gave greater water‐holding capacities. CONCLUSIONS: This work demonstrates the potential of unnatural amino acid hydrotropes as skin moisturizers and has developed some predictive ‘rules’ for further design and refinement of chemical structures. John Wiley and Sons Inc. 2016-07-24 2017-02 /pmc/articles/PMC5244679/ /pubmed/27380298 http://dx.doi.org/10.1111/ics.12351 Text en © 2016 The Authors. International Journal of Cosmetic Science published by John Wiley & Sons Ltd on behalf of Society of Cosmetic Scientists and Société Française de Cosmétologie. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Arezki, N. R.
Williams, A. C.
Cobb, A. J. A.
Brown, M. B.
Design, synthesis and characterization of linear unnatural amino acids for skin moisturization
title Design, synthesis and characterization of linear unnatural amino acids for skin moisturization
title_full Design, synthesis and characterization of linear unnatural amino acids for skin moisturization
title_fullStr Design, synthesis and characterization of linear unnatural amino acids for skin moisturization
title_full_unstemmed Design, synthesis and characterization of linear unnatural amino acids for skin moisturization
title_short Design, synthesis and characterization of linear unnatural amino acids for skin moisturization
title_sort design, synthesis and characterization of linear unnatural amino acids for skin moisturization
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244679/
https://www.ncbi.nlm.nih.gov/pubmed/27380298
http://dx.doi.org/10.1111/ics.12351
work_keys_str_mv AT arezkinr designsynthesisandcharacterizationoflinearunnaturalaminoacidsforskinmoisturization
AT williamsac designsynthesisandcharacterizationoflinearunnaturalaminoacidsforskinmoisturization
AT cobbaja designsynthesisandcharacterizationoflinearunnaturalaminoacidsforskinmoisturization
AT brownmb designsynthesisandcharacterizationoflinearunnaturalaminoacidsforskinmoisturization