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      Dual Bioactivities of Essential Oil Extracted from the Leaves of Artemisia argyi as an Antimelanogenic versus Antioxidant Agent and Chemical Composition Analysis by GC/MS

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          Abstract

          The study was aimed at investigating the antimelanogenic and antioxidant properties of essential oil when extracted from the leaves of Artemisia argyi, then analyzing the chemical composition of the essential oil. The inhibitory effect of the essential oil on melanogenesis was evaluated by a mushroom tyrosinase activity assay and B16F10 melanoma cell model. The antioxidant capacity of the essential oil was assayed by spectrophotometric analysis, and the volatile chemical composition of the essential oil was analyzed with gas chromatography-mass spectrometry (GC/MS). The results revealed that the essential oil significantly inhibits mushroom tyrosinase activity (IC 50 = 19.16 mg/mL), down-regulates B16F10 intracellular tyrosinase activity and decreases the amount of melanin content in a dose-dependent pattern. Furthermore, the essential oil significantly scavenged 2,2-diphenyl-1-picryl-hydrazyl (DPPH) and 2,2′-azino-bis (3-ethylbenzthiazoline- 6-sulphonic acid) ABTS radicals, showed an apparent reduction power as compared with metal-ion chelating activities. The chemicals constituents in the essential oil are ether (23.66%), alcohols (16.72%), sesquiterpenes (15.21%), esters (11.78%), monoterpenes (11.63%), ketones (6.09%), aromatic compounds (5.01%), and account for a 90.10% analysis of its chemical composition. It is predicted that eucalyptol and the other constituents, except for alcohols, in the essential oil may contribute to its antioxidant activities. The results indicated that essential oil extracted from A. argyi leaves decreased melanin production in B16F10 cells and showed potent antioxidant activity. The essential oil can thereby be applied as an inhibitor of melanogenesis and could also act as a natural antioxidant in skin care products.

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          Antioxidant activity applying an improved ABTS radical cation decolorization assay.

          A method for the screening of antioxidant activity is reported as a decolorization assay applicable to both lipophilic and hydrophilic antioxidants, including flavonoids, hydroxycinnamates, carotenoids, and plasma antioxidants. The pre-formed radical monocation of 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS*+) is generated by oxidation of ABTS with potassium persulfate and is reduced in the presence of such hydrogen-donating antioxidants. The influences of both the concentration of antioxidant and duration of reaction on the inhibition of the radical cation absorption are taken into account when determining the antioxidant activity. This assay clearly improves the original TEAC assay (the ferryl myoglobin/ABTS assay) for the determination of antioxidant activity in a number of ways. First, the chemistry involves the direct generation of the ABTS radical monocation with no involvement of an intermediary radical. Second, it is a decolorization assay; thus the radical cation is pre-formed prior to addition of antioxidant test systems, rather than the generation of the radical taking place continually in the presence of the antioxidant. Hence the results obtained with the improved system may not always be directly comparable with those obtained using the original TEAC assay. Third, it is applicable to both aqueous and lipophilic systems.
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            Studies on products of browning reaction. Antioxidative activities of products of browning reaction prepared from glucosamine.

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              Free radicals, antioxidants, and human disease: curiosity, cause, or consequence?

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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                Molecular Diversity Preservation International (MDPI)
                1422-0067
                2012
                12 November 2012
                : 13
                : 11
                : 14679-14697
                Affiliations
                [1 ]Department of Medical Laboratory Science and Biotechnology, China Medical University, No 91 Hsueh-Shih Road, Taichung 40402, Taiwan; E-Mail: lchuang@ 123456mail.cmu.edu.tw
                [2 ]Department of Hair styling & Design, Hung Kuang University, No. 34, Chung-Chie Road, Shalu, Taichung 43302, Taiwan; E-Mail: ygl615@ 123456yahoo.com.tw
                [3 ]Department of Applied Cosmetology & Master Program of Cosmetic Science, Hung Kuang University, No. 34, Chung-Chie Road, Shalu, Taichung 43302, Taiwan; E-Mail: khyih@ 123456sunrise.hk.edu.tw
                [4 ]General of Agriculture Bureau of Taichung City, No. 89, Sec 2, Taichung Port Road, Xitun Dist., Taichung 40701, Taiwan; E-Mail: m35208@ 123456taichung.gov.tw
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: ctm@ 123456sunrise.hk.edu.tw ; Tel.: +886-4-26318652 (ext. 5309/2216); Fax: +886-4-26321046.
                Article
                ijms-13-14679
                10.3390/ijms131114679
                3509604
                23203088
                30bb008f-b95f-4184-8d9c-510d61de098c
                © 2012 by the authors; licensee Molecular Diversity Preservation International, 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/3.0).

                History
                : 25 May 2012
                : 06 November 2012
                : 08 November 2012
                Categories
                Article

                Molecular biology
                tyrosinase,antioxidant,artemisia argyi,essential oil,melanin
                Molecular biology
                tyrosinase, antioxidant, artemisia argyi, essential oil, melanin

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