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Chemical composition and tyrosinase inhibitory activity of Cinnamomum cassia essential oil
BACKGROUND: Essential oils extracted from aromatic plants exhibit important biological activities and have become increasingly important for scientific research. The essential oil extracted from Cinnamomum cassia Presl (CC-EO) has various functional properties, however, little information is availab...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432840/ https://www.ncbi.nlm.nih.gov/pubmed/28510850 http://dx.doi.org/10.1186/1999-3110-54-10 |
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author | Chang, Chen-Tien Chang, Wen-Lun Hsu, Jaw-Cherng Shih, Ying Chou, Su-Tze |
author_facet | Chang, Chen-Tien Chang, Wen-Lun Hsu, Jaw-Cherng Shih, Ying Chou, Su-Tze |
author_sort | Chang, Chen-Tien |
collection | PubMed |
description | BACKGROUND: Essential oils extracted from aromatic plants exhibit important biological activities and have become increasingly important for scientific research. The essential oil extracted from Cinnamomum cassia Presl (CC-EO) has various functional properties, however, little information is available regarding the tyrosinase inhibitory activity. Therefore, the objectives of this study were to investigate the chemical composition and tyrosinase inhibitory activity of the CC-EO. RESULTS: cis-2-methoxycinnamic acid (43.06%) and cinnamaldehyde (42.37%) were found to be the two major components of the CC-EO identified by gas chromatography–mass spectrometry (GC-MS). The inhibitory activities of CC-EO and its major constituents were further evaluated against mushroom tyrosinase. The results showed that CC-EO and cinnamaldehyde exhibited anti-tyrosinase activities with IC(50) values of 6.16 ± 0.04 mg/mL and 4.04 ± 0.08 mg/mL, respectively. However, cis-2-methoxycinnamic acid did not show any anti-tyrosinase activity. The inhibition kinetics were analyzed by Lineweaver-Burk plots and second replots, which revealed that CC-EO and cinnamaldehyde were mixed-type inhibitors. The inhibition constants (Ki) for CC-EO and cinnamaldehyde were calculated to be 4.71 ± 0.09 mg/mL and 2.38 ± 0.09 mg/mL, respectively. CONCLUSION: These results demonstrate that CC-EO and its major component, cinnamaldehyde, possess potent anti-tyrosinase activities and may be a good source for skin-whitening agents. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1999-3110-54-10) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5432840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-54328402017-05-31 Chemical composition and tyrosinase inhibitory activity of Cinnamomum cassia essential oil Chang, Chen-Tien Chang, Wen-Lun Hsu, Jaw-Cherng Shih, Ying Chou, Su-Tze Bot Stud Research BACKGROUND: Essential oils extracted from aromatic plants exhibit important biological activities and have become increasingly important for scientific research. The essential oil extracted from Cinnamomum cassia Presl (CC-EO) has various functional properties, however, little information is available regarding the tyrosinase inhibitory activity. Therefore, the objectives of this study were to investigate the chemical composition and tyrosinase inhibitory activity of the CC-EO. RESULTS: cis-2-methoxycinnamic acid (43.06%) and cinnamaldehyde (42.37%) were found to be the two major components of the CC-EO identified by gas chromatography–mass spectrometry (GC-MS). The inhibitory activities of CC-EO and its major constituents were further evaluated against mushroom tyrosinase. The results showed that CC-EO and cinnamaldehyde exhibited anti-tyrosinase activities with IC(50) values of 6.16 ± 0.04 mg/mL and 4.04 ± 0.08 mg/mL, respectively. However, cis-2-methoxycinnamic acid did not show any anti-tyrosinase activity. The inhibition kinetics were analyzed by Lineweaver-Burk plots and second replots, which revealed that CC-EO and cinnamaldehyde were mixed-type inhibitors. The inhibition constants (Ki) for CC-EO and cinnamaldehyde were calculated to be 4.71 ± 0.09 mg/mL and 2.38 ± 0.09 mg/mL, respectively. CONCLUSION: These results demonstrate that CC-EO and its major component, cinnamaldehyde, possess potent anti-tyrosinase activities and may be a good source for skin-whitening agents. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1999-3110-54-10) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-08-21 /pmc/articles/PMC5432840/ /pubmed/28510850 http://dx.doi.org/10.1186/1999-3110-54-10 Text en © Chang et al.; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Chang, Chen-Tien Chang, Wen-Lun Hsu, Jaw-Cherng Shih, Ying Chou, Su-Tze Chemical composition and tyrosinase inhibitory activity of Cinnamomum cassia essential oil |
title | Chemical composition and tyrosinase inhibitory activity of Cinnamomum cassia essential oil |
title_full | Chemical composition and tyrosinase inhibitory activity of Cinnamomum cassia essential oil |
title_fullStr | Chemical composition and tyrosinase inhibitory activity of Cinnamomum cassia essential oil |
title_full_unstemmed | Chemical composition and tyrosinase inhibitory activity of Cinnamomum cassia essential oil |
title_short | Chemical composition and tyrosinase inhibitory activity of Cinnamomum cassia essential oil |
title_sort | chemical composition and tyrosinase inhibitory activity of cinnamomum cassia essential oil |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432840/ https://www.ncbi.nlm.nih.gov/pubmed/28510850 http://dx.doi.org/10.1186/1999-3110-54-10 |
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