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 (IC50 = 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.

Highlights

  • Melanin is a dark pigment produced by epidermal melanocytes

  • We examined the inhibitory effects on melanogenesis and antioxidant capacity of essential oil extracted from leaves of A. argyi and analyzed its chemical composition by gas chromatography-mass spectrometry (GC/MS)

  • To determine the potential inhibitory effect of A. argyi essential oil on mushroom tyrosinase activity, enzyme inhibition experiments were done in triplicate

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Summary

Introduction

Melanin is a dark pigment produced by epidermal melanocytes. It is responsible for skin color and plays an important role in protecting the skin from UV light-induced damage. Many skin depigmenting chemicals such as kojic acid [4], arbutin [5] and azelaic acid [6], which act as tyrosinase inhibitors, have been applied in skin whitening products for the treatment or prevention of abnormal skin pigmentation [7]. The chemical composition of essential oils extracted from leaves or flowers of A. argyi has been reported [32,33]. We examined the inhibitory effects on melanogenesis and antioxidant capacity of essential oil extracted from leaves of A. argyi and analyzed its chemical composition by GC/MS. Antimelanogenic versus antioxidant efficacy of A. argyi essential oil and its chemical composition are reported in the present study

Results and Discussion
DPPH Scavenging Capacity Assay
ABTS Scavenging Ability Assay
Plant Material and Extraction of Essential Oils
Mushroom Tyrosinase Actvity Measurement
B16F10 Intracellular Melanin Content Measurement
B16F10 Intracellular Tyrosinase Activity Assay
DPPH Scavenging Activity Assay
Determination of Reducing Power
Measurement of Metal-Ion Chelating Capacity
3.10. Statistical Analysis
Conclusions
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