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dc.contributor.authorAhmed, Shakeel
dc.contributor.authorSinan, Kouadio Ibrahime
dc.contributor.authorNilofar, Claudio
dc.contributor.authorFerrante, Claudio
dc.contributor.authorEyupoğlu, Ozan Emre
dc.contributor.authorEtienne, Ouattara Katinan
dc.contributor.authorZengin, Gökhan
dc.date.accessioned2023-12-25T07:44:55Z
dc.date.available2023-12-25T07:44:55Z
dc.date.issued2023en_US
dc.identifier.citationAhmed, S., Sinan, K. I., Nilofar, C., Ferrante, C., Eyupoğlu, O. E., Etienne, O. K. ... Zengin, G. (2023). Online-HPLC strategies, antioxidant and enzyme inhibitory activities of different extracts of mondia whitei leaves. Journal of Biological Regulators and Homeostatic Agents, 37(11), 6029-6039. https://dx.doi.org/10.23812/j.biol.regul.homeost.agents.20233711.577en_US
dc.identifier.issn0393-974X
dc.identifier.issn1724-6083
dc.identifier.urihttps://dx.doi.org/10.23812/j.biol.regul.homeost.agents.20233711.577
dc.identifier.urihttps://hdl.handle.net/20.500.12511/12066
dc.description.abstractBackground: Mondia whitei, an indigenous African plant, is widely recognised for its medicinal properties. Throughout ancient times, African communities have employed this remedy to address a wide range of health conditions. However, there is a lack of online High-Performance Liquid Chromatography (HPLC) studies available for this plant. The present investigation aimed to address and alleviate this deficiency by providing a comprehensive analysis.Methods: Methanol, combination of water and methanol, ethyl acetate, and water extracts of Mondia whitei (M. whitei) leaves were utilized in this study. The phenolic and flavonoids composition of the extracts determined by Folin-Ciocalteu and Aluminum chloride (AlCl3) assays, respectively. The antioxidant potential of all the extracts was assessed through a range of in vitro assays, including FRAP (Ferric reducing antioxidant power), DPPH (2,2-diphenyl-1-picrylhydrazyl), ABTS [2,2 '-Azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid)], CUPRAC (cupric reducing antioxidant capacity), PBD (phosphomolybdenum), and MCA (metal chelating ability). Subsequently, the online HPLC-linked system had established to compare these extracts using four distinct antioxidant analysis methods: FRAP, DPPH, ABTS, and CUPRAC. The enzyme inhibitory properties were also investigated against cholinesterases, tyrosinase, alpha-amylase and alpha-glucosidase.Results: The methanol-water and methanol extracts had the highest phenolic contents and demonstrated superior efficacy as scavenging/reducing agents and enzyme inhibitors, particularly against tyrosinase and cholinesterase (p < 0.05). Through the utilisation of various online HPLC antioxidant techniques, the identification of four molecules exhibiting antioxidant activity was achieved. These compounds were identified as Coumarin, Vanillin, p-OH benzoic acid, and Chlorogenic acid.Conclusions: Mondia whitei leaves can be regarded as a valuable source of natural bioactive compounds, with the potential to serve as a material basis for pharmacological effects in nutraceutical and pharmaceutical applications.en_US
dc.language.isoengen_US
dc.publisherBiolife Sasen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMondia Whiteien_US
dc.subjectOnline HPLC Assaysen_US
dc.subjectAntioxidantsen_US
dc.subjectEnzyme Inhibitorsen_US
dc.titleOnline-HPLC strategies, antioxidant and enzyme inhibitory activities of different extracts of mondia whitei leavesen_US
dc.typearticleen_US
dc.relation.ispartofJournal of Biological Regulators and Homeostatic Agentsen_US
dc.departmentİstanbul Medipol Üniversitesi, Eczacılık Fakültesi, Temel Eczacılık Bilimleri Bölümü, Biyokimya Ana Bilim Dalıen_US
dc.authorid0000-0002-4449-0537en_US
dc.identifier.volume37en_US
dc.identifier.issue11en_US
dc.identifier.startpage6029en_US
dc.identifier.endpage6039en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.23812/j.biol.regul.homeost.agents.20233711.577en_US
dc.institutionauthorEyupoğlu, Ozan Emre
dc.identifier.wosqualityQ2en_US
dc.identifier.wos001114250800001en_US


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