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Cytotoxic and enzyme inhibitory potential of two potentilla species (P. speciosa L. and P. reptans Willd.) and their chemical composition
Scopus
Open Access Toplam 345 atıf DOI
In this work, the biological and chemical fingerprints of three extracts (ethyl acetate, methanol, and water) from two Potentilla species (Potentilla reptans and P. speciosa) were investigated. Antioxidant, enzyme inhibitory, and cytotoxic activities were performed for the biological fingerprint. For the chemical characterization, total bioactive components, and individual phenolic components were determined using photometric and HPLC methods, respectively. The main identified phenolic compounds in these extracts were rutin and catechin. Methanol and water extracts contained the highest total phenolic and flavonoid content. The results of antioxidant assays showed that methanol and water extracts displayed higher antioxidant activity compared to the ethyl acetate extract. Generally, methanol and water extracts exhibited higher biological activities correlated with higher levels the bioactive components. For P. speciosa, the methanol extract exhibited the highest enzyme inhibitory activity (except BChE inhibitory activity). P. reptans exhibited also high antiproliferative activity against MCF-7 cells whilst P. speciosa had weak to moderate activity against both of A549 and MCF-7 cell lines. The results suggest that Potentilla species could be potential candidates for developing new phyto-pharmaceuticals and functional ingredients.
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Comparative metabolic profiling, enzyme inhibitory activities, and in-silico analysis of the hexane extract and the hydrodistilled oil of Boswellia serrata
Scopus
Havuzumuzda Open Access 1 atıf almış
Frankincense (Boswellia spp.) oleogum resin is a valuable natural source of bioactive phytoconstituents with diverse therapeutic potential. In this study, the hydrodistilled essential oil (EO) and n-hexane extract (HE) of Boswellia serrata gums were analyzed through gas chromatography–mass spectrometry (GC-MS) to determine their phytochemical composition. The GC-MS results in the identification of 62 and 71 components in the EO and HE, respectively. Acetic acid octyl ester (41.09%) and nerolidol (13.64%), were the major components of the EO. Meanwhile, incensole (28.56%), (1S,2E,4S,5R,7E,11E)-cembra-2,7,11-trien-4,5-diol (13.54%), and 24-norursa-3,12-diene (9.25%) in the HE. Regarding the antioxidant effects, the EO exhibited significantly higher antioxidant capacity compared to the HE (DPPH: 9.24 and 6.50 mg TE/g; ABTS: 25.71 and 4.94 mg TE/g), respectively. Moreover, the EO was more potent in the CUPRAC test (61.12 mg TE/g for the essential oil and 50.62 mg TE/g for HE), while the n-hexane extract (72.68 mg TE/g) showed stronger ability than the EO (13.22 mg TE/g) in the FRAP assay. The EO had a higher ability in phosphomolybdenum and metal chelation tests in comparison with the HE extracts. Further, the oil showed more potent inhibitory activity against cholinesterase, α-glucosidase, and tyrosinase than the HE extract. The HE extract was only more active on α-amylase compared to the oil. These findings suggest that olibanum EO possesses potent bioactive compounds that may contribute to the management of oxidative stress and age-related conditions, including Alzheimer’s disease, diabetes mellitus, and skin hyperpigmentation.
Atıf Yapan Makale Bilgileri
Kurumlar (8)
Faculty of Pharmacy
Kafr el-sheikh, Egypt
Faculty of Pharmacy
Cairo, Egypt
Faculty of Pharmacy
Alexandria, Egypt
Faculty of Pharmacy, Ain Shams University
Cairo, Egypt
Field of Pharmacy
Ras Sedr, Egypt
King Khalid University
Abha, Saudi Arabia
Selçuk Üniversitesi
Selçuklu, Turkey
University of G. d'Annunzio Chieti and Pescara
Chieti, Italy