Pistacia lentiscus L. Distilled Leaves as a Potential Cosmeceutical Ingredient: Phytochemical Characterization, Transdermal Diffusion, and Anti‐Elastase and Anti‐Tyrosinase Activities
Author | Elloumi, Wiem |
Author | Maalej, Amina |
Author | Ortiz, Sergio |
Author | Michel, Sylvie |
Author | Chamkha, Mohamed |
Author | Boutefnouchet, Sabrina |
Author | Sayadi, Sami |
Available date | 2022-03-27T05:43:11Z |
Publication Date | 2022-02-01 |
Publication Name | Molecules |
Identifier | http://dx.doi.org/10.3390/molecules27030855 |
Citation | The authors are grateful to the Qatar National Research Fund (QNRF) for funding and supporting the M-NEX Project (grant no. BFSUGI01-1120-170005) in Qatar. The M-NEX is a project of the Collaborative Research Area Belmont Forum (no. 11314551). |
Abstract | The present work was performed to investigate the phenolic composition of P. lentiscus L. distilled leaves (PDL) and examine its potential against certain key enzymes related to skin aging. High‐pressure liquid chromatography coupled to mass spectrometry (HPLC‐MS) and various separation procedures combined with nuclear magnetic resonance (NMR) and MS analysis were performed to isolate and identify compounds present in the ethyl acetate extract (EAE) of PDL. A high amount of flavonol glycoside was detected in EAE. Indeed, quercetin‐3‐O‐rhamnoside (FC), myri-cetin‐3‐O‐rhamnoside (FM2), and kaempferol‐3‐O‐rhamnoside (FB2) were isolated from EAE, and are present in high quantities of 10.47 ± 0.26, 12.17 ± 0.74, and 4.53 ± 0.59 mg/g dry weight, respec-tively. A transdermal diffusion study was carried out to determine the EAE‐molecules that may transmit the cutaneous barrier and showed that FM2 transmits the membrane barrier with a high amount followed by FC. EAE, FM2, and FC were tested against tyrosinase and elastase enzymes. Moreover, intracellular tyrosinase inhibition and cytotoxicity on skin melanoma cells (B16) were evaluated. The results indicated that EAE, FC, and FM2 have important inhibitory activities com-pared to the well‐known standards, at non‐cytotoxic concentrations. Therefore, they could be excel-lent agents for treating skin pigmentation and elasticity problems. |
Sponsor | The authors are grateful to the Qatar National Research Fund (QNRF) for funding and supporting the M-NEX Project (grant no. BFSUGI01-1120-170005) in Qatar. The M-NEX is a project of the Collaborative Research Area Belmont Forum (no. 11314551). |
Language | en |
Publisher | MDPI |
Subject | Cytotoxicity Elastase inhibition LC‐MS Myricetin‐3‐O‐rhamnoside Nuclear magnetic resonance Pistacia lentiscus L. leaves Quercetin‐3‐O‐rhamnoside Transdermal diffusion Tyrosinase inhibition |
Type | Article |
Issue Number | 3 |
Volume Number | 27 |
ESSN | 1420-3049 |
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