Phytochemical Analysis of Euphorbia greenwayi Aerial Parts: Antioxidant and Anti-inflammatory Potential | ||
| Egyptian Journal of Chemistry | ||
| Volume 67, Issue 3, March 2024, Pages 515-525 PDF (464.37 K) | ||
| Document Type: Original Article | ||
| DOI: 10.21608/ejchem.2023.230525.8459 | ||
| Authors | ||
| Ahmed Zaghlol1; zeinab kandil2; Miriam yousif* 3; Riham Salah El Dine4; Wafaa Elkady5 | ||
| 1Department of pharmacognosy and medicinal plants, Faculty of Pharmacy, Future University in Egypt, Cairo, Egypt | ||
| 2Pharmacognosy Department, Faculty of Pharmacy, Cairo University, Eygpt | ||
| 3Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo | ||
| 4Pharmacognosy Department, Faculty of Pharmacy, Cairo University | ||
| 5Department of Pharmacognosy and Medicinal Plants, Faculty of Pharmacy, Future University in Egypt | ||
| Abstract | ||
| Euphorbia greenwayi P.R.O. Bally & S. Carter, is a member of the Euphorbiaceae family, which includes numerous species used in folk medicine to cure a variety of diseases. However, there have been few reports regarding this species. E. greenwayi aerial parts’ analysis was done using UPLC-MS/MS technique for methanol extract (ME). The negative ion mode resulted in the identification of three phenolic acids; chlorogenic, ferloyl malic acids, and brevifolin carboxylic acid hexoside. Four flavonoids; rutin, astragalin, kaempferol-O-acetyl-hexoside, and isorhamnetin-O-rutinoside. Additionally, eight diterpenes were identified as ingenol mebutate, deoxy-oxoingenol butanoate, and ingenol dibenzoate with its isomer, besides, phorbol acetate, phorbol diacetate and its isomer, and phorbol. Also, five triterpenes; taraxasterol, lupeol, β-Sitosterol, hydroxytaraxasterol, and hydroxyoleanolic acid were detected by the positive ion mode. ME was fractionated using chloroform (CF) and ethyl acetate (EF) to evaluate phenolic and flavonoid contents, antioxidant, and anti-inflammatory potential. EF had the greatest flavonoid and phenolic content 141±9 μg RE/mg & 108.76±3 μg GAE/mg, respectively. EF exhibited the highest antioxidant activity in DPPH, metal chelation, and ORAC assays: 30.14±1 μg/mL, 7.36±0.4 μmole EDTA eq/mg, and 7118.83±4 µmole Trolox eq/mg respectively. ME revealed the highest anti-inflammatory activity against the expression of TNF-α and IL6 cytokines 0.241±0.01 and 0.321±0.02 fold change respectively. | ||
| Keywords | ||
| anti-inflammatory; antioxidant; Euphorbia greenwayi; Euphorbiaceae; flavonoids; phenolic acids; terpenes | ||
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