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New lupeol esters as active substances in the treatment of skin damage
The purpose of the research was to obtain new derivatives of natural triterpene lupeol and to evaluate their potential as active substances in the treatment of skin damage. Four new lupeol esters (propionate, succinate, isonicotinate and acetylsalicylate) and lupeol acetate were obtained using an ec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438679/ https://www.ncbi.nlm.nih.gov/pubmed/30921370 http://dx.doi.org/10.1371/journal.pone.0214216 |
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author | Malinowska, Magdalena Miroslaw, Barbara Sikora, Elzbieta Ogonowski, Jan Wojtkiewicz, Agnieszka M. Szaleniec, Maciej Pasikowska-Piwko, Monika Eris, Irena |
author_facet | Malinowska, Magdalena Miroslaw, Barbara Sikora, Elzbieta Ogonowski, Jan Wojtkiewicz, Agnieszka M. Szaleniec, Maciej Pasikowska-Piwko, Monika Eris, Irena |
author_sort | Malinowska, Magdalena |
collection | PubMed |
description | The purpose of the research was to obtain new derivatives of natural triterpene lupeol and to evaluate their potential as active substances in the treatment of skin damage. Four new lupeol esters (propionate, succinate, isonicotinate and acetylsalicylate) and lupeol acetate were obtained using an eco-friendly synthesis method. In the esterification process, the commonly used hazardous reagents in this type of synthesis were replaced by safe ones. This unconventional, eco-friendly, method is particularly important because the compounds obtained are potentially active substances in skin care formulations. Even trace amounts of hazardous reagents can have a toxic effect on damaged or irritated tissues. The molecular structure of the esters were confirmed by (1)H NMR, (13)C NMR and IR spectroscopy methods. Their crystal structures were determined using XRD method. To complete the analysis of their characteristics, physicochemical properties (melting point, lipophilicity, water solubility) and biological activity of the lupeol derivatives were studied. Results of an irritant potential test, carried out on Reconstructed Human Epidermis (RHE), confirmed that the synthesized lupeol derivatives are not cytotoxic and they stimulate a process of human cell proliferation. The safety of use for tested compounds was determined in a cell viability test (cytotoxicity detection kit based on the measurement of lactate dehydrogenase activity) for keratinocytes and fibroblasts. The results obtained showed that the modification of lupeol structure improve its bioavailability and activity. All of the esters penetrate the stratum corneum and the upper layers of the dermis better than the maternal lupeol. Lupeol isonicotinate, acetate and propionate were the most effective compounds in a stimulation of the human skin cell proliferation process. This combination resulted in an increase in the concentration of cells of more than 30% in comparison to control samples. The results indicate that the chemical modification of lupeol allows to obtain promising active substances for treatment of skin damage, including thermal, chemical and radiation burns. |
format | Online Article Text |
id | pubmed-6438679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64386792019-04-12 New lupeol esters as active substances in the treatment of skin damage Malinowska, Magdalena Miroslaw, Barbara Sikora, Elzbieta Ogonowski, Jan Wojtkiewicz, Agnieszka M. Szaleniec, Maciej Pasikowska-Piwko, Monika Eris, Irena PLoS One Research Article The purpose of the research was to obtain new derivatives of natural triterpene lupeol and to evaluate their potential as active substances in the treatment of skin damage. Four new lupeol esters (propionate, succinate, isonicotinate and acetylsalicylate) and lupeol acetate were obtained using an eco-friendly synthesis method. In the esterification process, the commonly used hazardous reagents in this type of synthesis were replaced by safe ones. This unconventional, eco-friendly, method is particularly important because the compounds obtained are potentially active substances in skin care formulations. Even trace amounts of hazardous reagents can have a toxic effect on damaged or irritated tissues. The molecular structure of the esters were confirmed by (1)H NMR, (13)C NMR and IR spectroscopy methods. Their crystal structures were determined using XRD method. To complete the analysis of their characteristics, physicochemical properties (melting point, lipophilicity, water solubility) and biological activity of the lupeol derivatives were studied. Results of an irritant potential test, carried out on Reconstructed Human Epidermis (RHE), confirmed that the synthesized lupeol derivatives are not cytotoxic and they stimulate a process of human cell proliferation. The safety of use for tested compounds was determined in a cell viability test (cytotoxicity detection kit based on the measurement of lactate dehydrogenase activity) for keratinocytes and fibroblasts. The results obtained showed that the modification of lupeol structure improve its bioavailability and activity. All of the esters penetrate the stratum corneum and the upper layers of the dermis better than the maternal lupeol. Lupeol isonicotinate, acetate and propionate were the most effective compounds in a stimulation of the human skin cell proliferation process. This combination resulted in an increase in the concentration of cells of more than 30% in comparison to control samples. The results indicate that the chemical modification of lupeol allows to obtain promising active substances for treatment of skin damage, including thermal, chemical and radiation burns. Public Library of Science 2019-03-28 /pmc/articles/PMC6438679/ /pubmed/30921370 http://dx.doi.org/10.1371/journal.pone.0214216 Text en © 2019 Malinowska et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Malinowska, Magdalena Miroslaw, Barbara Sikora, Elzbieta Ogonowski, Jan Wojtkiewicz, Agnieszka M. Szaleniec, Maciej Pasikowska-Piwko, Monika Eris, Irena New lupeol esters as active substances in the treatment of skin damage |
title | New lupeol esters as active substances in the treatment of skin damage |
title_full | New lupeol esters as active substances in the treatment of skin damage |
title_fullStr | New lupeol esters as active substances in the treatment of skin damage |
title_full_unstemmed | New lupeol esters as active substances in the treatment of skin damage |
title_short | New lupeol esters as active substances in the treatment of skin damage |
title_sort | new lupeol esters as active substances in the treatment of skin damage |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438679/ https://www.ncbi.nlm.nih.gov/pubmed/30921370 http://dx.doi.org/10.1371/journal.pone.0214216 |
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