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Tyrosinase-based TLC Autography for anti-melanogenic drug screening

Tyrosinase-based TLC (thin layer chromatography) was developed for screening of anti-melanogenic drugs. In particular, this technique enables researchers to identify melanogenic inhibitor(s) in tested mixtures with the naked eye. In comparison with traditional colorimetric screening assays for tyros...

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Autores principales: Hsu, Kai-Di, Chan, Yu-Hin, Chen, Hong-Jhang, Lin, Shi-Ping, Cheng, Kuan-Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762723/
https://www.ncbi.nlm.nih.gov/pubmed/29321636
http://dx.doi.org/10.1038/s41598-017-18720-0
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author Hsu, Kai-Di
Chan, Yu-Hin
Chen, Hong-Jhang
Lin, Shi-Ping
Cheng, Kuan-Chen
author_facet Hsu, Kai-Di
Chan, Yu-Hin
Chen, Hong-Jhang
Lin, Shi-Ping
Cheng, Kuan-Chen
author_sort Hsu, Kai-Di
collection PubMed
description Tyrosinase-based TLC (thin layer chromatography) was developed for screening of anti-melanogenic drugs. In particular, this technique enables researchers to identify melanogenic inhibitor(s) in tested mixtures with the naked eye. In comparison with traditional colorimetric screening assays for tyrosinase inhibitor(s), not only is tyrosinase-based TLC a more cost-effective option (nearly one-tenth the enzyme cost of colorimetric methods) but also is a more sensitive detection approach for kojic acid (KA), a standard anti-melanogenic drug. The detection limit of tyrosinase-based TLC and colorimetric tyrosinase assay for KA was 0.0125 and 1.25 μg, respectively, demonstrating that the former was 100-fold more sensitive than the latter to determine the tyrosinase inhibitory rate of KA. Furthermore, the results of this method have demonstrated excellent precision by Gage Repeatability and Reproducibility (Gage R&R), with the variation of total Gage R&R being 28.24%. To verify the applicability of tyrosinase-based TLC, this platform was employed to screen melanogenic inhibitor(s) from Ganoderma formosanum extracts and two of all fractions (GFE-EA F4, F5) obtained showed depigmenting activity. It is noteworthy that these two fractions also exerted anti-melanogenesis activity on zebrafish, therefore verifying the credibility of tyrosinase-based TLC. In sum, this technique provides new insight into the discovery of novel melanogenic inhibitor(s).
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spelling pubmed-57627232018-01-17 Tyrosinase-based TLC Autography for anti-melanogenic drug screening Hsu, Kai-Di Chan, Yu-Hin Chen, Hong-Jhang Lin, Shi-Ping Cheng, Kuan-Chen Sci Rep Article Tyrosinase-based TLC (thin layer chromatography) was developed for screening of anti-melanogenic drugs. In particular, this technique enables researchers to identify melanogenic inhibitor(s) in tested mixtures with the naked eye. In comparison with traditional colorimetric screening assays for tyrosinase inhibitor(s), not only is tyrosinase-based TLC a more cost-effective option (nearly one-tenth the enzyme cost of colorimetric methods) but also is a more sensitive detection approach for kojic acid (KA), a standard anti-melanogenic drug. The detection limit of tyrosinase-based TLC and colorimetric tyrosinase assay for KA was 0.0125 and 1.25 μg, respectively, demonstrating that the former was 100-fold more sensitive than the latter to determine the tyrosinase inhibitory rate of KA. Furthermore, the results of this method have demonstrated excellent precision by Gage Repeatability and Reproducibility (Gage R&R), with the variation of total Gage R&R being 28.24%. To verify the applicability of tyrosinase-based TLC, this platform was employed to screen melanogenic inhibitor(s) from Ganoderma formosanum extracts and two of all fractions (GFE-EA F4, F5) obtained showed depigmenting activity. It is noteworthy that these two fractions also exerted anti-melanogenesis activity on zebrafish, therefore verifying the credibility of tyrosinase-based TLC. In sum, this technique provides new insight into the discovery of novel melanogenic inhibitor(s). Nature Publishing Group UK 2018-01-10 /pmc/articles/PMC5762723/ /pubmed/29321636 http://dx.doi.org/10.1038/s41598-017-18720-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hsu, Kai-Di
Chan, Yu-Hin
Chen, Hong-Jhang
Lin, Shi-Ping
Cheng, Kuan-Chen
Tyrosinase-based TLC Autography for anti-melanogenic drug screening
title Tyrosinase-based TLC Autography for anti-melanogenic drug screening
title_full Tyrosinase-based TLC Autography for anti-melanogenic drug screening
title_fullStr Tyrosinase-based TLC Autography for anti-melanogenic drug screening
title_full_unstemmed Tyrosinase-based TLC Autography for anti-melanogenic drug screening
title_short Tyrosinase-based TLC Autography for anti-melanogenic drug screening
title_sort tyrosinase-based tlc autography for anti-melanogenic drug screening
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762723/
https://www.ncbi.nlm.nih.gov/pubmed/29321636
http://dx.doi.org/10.1038/s41598-017-18720-0
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