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Characterization of Melanogenesis Inhibitory Constituents of Morus alba Leaves and Optimization of Extraction Conditions Using Response Surface Methodology

Melanin is a natural pigment that plays an important role in the protection of skin, however, hyperpigmentation cause by excessive levels of melatonin is associated with several problems. Therefore, melanogenesis inhibitory natural products have been developed by the cosmetic industry as skin medica...

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Autores principales: Jeong, Ji Yeon, Liu, Qing, Kim, Seon Beom, Jo, Yang Hee, Mo, Eun Jin, Yang, Hyo Hee, Song, Dae Hye, Hwang, Bang Yeon, Lee, Mi Kyeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272263/
https://www.ncbi.nlm.nih.gov/pubmed/26007176
http://dx.doi.org/10.3390/molecules20058730
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author Jeong, Ji Yeon
Liu, Qing
Kim, Seon Beom
Jo, Yang Hee
Mo, Eun Jin
Yang, Hyo Hee
Song, Dae Hye
Hwang, Bang Yeon
Lee, Mi Kyeong
author_facet Jeong, Ji Yeon
Liu, Qing
Kim, Seon Beom
Jo, Yang Hee
Mo, Eun Jin
Yang, Hyo Hee
Song, Dae Hye
Hwang, Bang Yeon
Lee, Mi Kyeong
author_sort Jeong, Ji Yeon
collection PubMed
description Melanin is a natural pigment that plays an important role in the protection of skin, however, hyperpigmentation cause by excessive levels of melatonin is associated with several problems. Therefore, melanogenesis inhibitory natural products have been developed by the cosmetic industry as skin medications. The leaves of Morus alba (Moraceae) have been reported to inhibit melanogenesis, therefore, characterization of the melanogenesis inhibitory constituents of M. alba leaves was attempted in this study. Twenty compounds including eight benzofurans, 10 flavonoids, one stilbenoid and one chalcone were isolated from M. alba leaves and these phenolic constituents were shown to significantly inhibit tyrosinase activity and melanin content in B6F10 melanoma cells. To maximize the melanogenesis inhibitory activity and active phenolic contents, optimized M. alba leave extraction conditions were predicted using response surface methodology as a methanol concentration of 85.2%; an extraction temperature of 53.2 °C and an extraction time of 2 h. The tyrosinase inhibition and total phenolic content under optimal conditions were found to be 74.8% inhibition and 24.8 μg GAE/mg extract, which were well-matched with the predicted values of 75.0% inhibition and 23.8 μg GAE/mg extract. These results shall provide useful information about melanogenesis inhibitory constituents and optimized extracts from M. alba leaves as cosmetic therapeutics to reduce skin hyperpigmentation.
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spelling pubmed-62722632019-01-07 Characterization of Melanogenesis Inhibitory Constituents of Morus alba Leaves and Optimization of Extraction Conditions Using Response Surface Methodology Jeong, Ji Yeon Liu, Qing Kim, Seon Beom Jo, Yang Hee Mo, Eun Jin Yang, Hyo Hee Song, Dae Hye Hwang, Bang Yeon Lee, Mi Kyeong Molecules Article Melanin is a natural pigment that plays an important role in the protection of skin, however, hyperpigmentation cause by excessive levels of melatonin is associated with several problems. Therefore, melanogenesis inhibitory natural products have been developed by the cosmetic industry as skin medications. The leaves of Morus alba (Moraceae) have been reported to inhibit melanogenesis, therefore, characterization of the melanogenesis inhibitory constituents of M. alba leaves was attempted in this study. Twenty compounds including eight benzofurans, 10 flavonoids, one stilbenoid and one chalcone were isolated from M. alba leaves and these phenolic constituents were shown to significantly inhibit tyrosinase activity and melanin content in B6F10 melanoma cells. To maximize the melanogenesis inhibitory activity and active phenolic contents, optimized M. alba leave extraction conditions were predicted using response surface methodology as a methanol concentration of 85.2%; an extraction temperature of 53.2 °C and an extraction time of 2 h. The tyrosinase inhibition and total phenolic content under optimal conditions were found to be 74.8% inhibition and 24.8 μg GAE/mg extract, which were well-matched with the predicted values of 75.0% inhibition and 23.8 μg GAE/mg extract. These results shall provide useful information about melanogenesis inhibitory constituents and optimized extracts from M. alba leaves as cosmetic therapeutics to reduce skin hyperpigmentation. MDPI 2015-05-14 /pmc/articles/PMC6272263/ /pubmed/26007176 http://dx.doi.org/10.3390/molecules20058730 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jeong, Ji Yeon
Liu, Qing
Kim, Seon Beom
Jo, Yang Hee
Mo, Eun Jin
Yang, Hyo Hee
Song, Dae Hye
Hwang, Bang Yeon
Lee, Mi Kyeong
Characterization of Melanogenesis Inhibitory Constituents of Morus alba Leaves and Optimization of Extraction Conditions Using Response Surface Methodology
title Characterization of Melanogenesis Inhibitory Constituents of Morus alba Leaves and Optimization of Extraction Conditions Using Response Surface Methodology
title_full Characterization of Melanogenesis Inhibitory Constituents of Morus alba Leaves and Optimization of Extraction Conditions Using Response Surface Methodology
title_fullStr Characterization of Melanogenesis Inhibitory Constituents of Morus alba Leaves and Optimization of Extraction Conditions Using Response Surface Methodology
title_full_unstemmed Characterization of Melanogenesis Inhibitory Constituents of Morus alba Leaves and Optimization of Extraction Conditions Using Response Surface Methodology
title_short Characterization of Melanogenesis Inhibitory Constituents of Morus alba Leaves and Optimization of Extraction Conditions Using Response Surface Methodology
title_sort characterization of melanogenesis inhibitory constituents of morus alba leaves and optimization of extraction conditions using response surface methodology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272263/
https://www.ncbi.nlm.nih.gov/pubmed/26007176
http://dx.doi.org/10.3390/molecules20058730
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