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AuthorElloumi, Wiem
AuthorMaalej, Amina
AuthorOrtiz, Sergio
AuthorMichel, Sylvie
AuthorChamkha, Mohamed
AuthorBoutefnouchet, Sabrina
AuthorSayadi, Sami
Available date2022-03-27T05:43:11Z
Publication Date2022-02-01
Publication NameMolecules
Identifierhttp://dx.doi.org/10.3390/molecules27030855
CitationThe 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).
URIhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85123556886&origin=inward
URIhttp://hdl.handle.net/10576/29021
AbstractThe 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.
SponsorThe 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).
Languageen
PublisherMDPI
SubjectCytotoxicity
Elastase inhibition
LC‐MS
Myricetin‐3‐O‐rhamnoside
Nuclear magnetic resonance
Pistacia lentiscus L. leaves
Quercetin‐3‐O‐rhamnoside
Transdermal diffusion
Tyrosinase inhibition
TitlePistacia lentiscus L. Distilled Leaves as a Potential Cosmeceutical Ingredient: Phytochemical Characterization, Transdermal Diffusion, and Anti‐Elastase and Anti‐Tyrosinase Activities
TypeArticle
Issue Number3
Volume Number27
ESSN1420-3049


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