Analyzing the Chemical Constituents and In Vitro Biological Effects of Extracts Artemisia absinthium L. Extracts Obtained Using Different Methodologies and Solvents

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Özet

The present study aimed to investigate the chemical constituents of different extracts from aerial parts of A. absinthium and to evaluate their antioxidant and enzyme inhibition activity. Extracts were prepared by maceration, infusion or Soxhlet techniques. Results showed that the highest total phenolic and flavonoids contents was recorded respectively from the hexane extract prepared by maceration and ethyl acetate extract obtained by Soxhlet method. The characteristic compounds of Artemisia species artemetin, casticin, sesartemin and yangambin in addition to coumarins were identified in all extracts. Aqueous extract obtained by infusion exerted the highest radical scavenging and ions reducing properties while that prepared by maceration displayed the highest chelating power. Methanol extracts obtained by the two methods of extraction exerted the highest anti-Tyr activity while that obtained by maceration showed the best α-glucosidase inhibition activity. These findings indicated that A. absinthium is a rich source of bioactive molecules with possible therapeutic applications.

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https://rdlopen.rawdatalibrary.net/r/munzur/1547Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/cbdv.202400893Yayıncı resmi DOI adresi
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorYagi, Sakina
dc.contributor.authorZengin, Gokhan
dc.contributor.authorIbrahime Sinan, Kouadio
dc.contributor.authorYavuz Paksoy, Mehmet
dc.contributor.authorCziáky, Zoltán
dc.contributor.authorJekő, József
dc.contributor.authorDall'Acqua, Stefano
dc.date.accessioned2026-10-28T14:54:19.616342817Z
dc.date.available2026-10-28T14:54:19.616342817Z
dc.date.issued2024
dc.description.abstractThe present study aimed to investigate the chemical constituents of different extracts from aerial parts of A. absinthium and to evaluate their antioxidant and enzyme inhibition activity. Extracts were prepared by maceration, infusion or Soxhlet techniques. Results showed that the highest total phenolic and flavonoids contents was recorded respectively from the hexane extract prepared by maceration and ethyl acetate extract obtained by Soxhlet method. The characteristic compounds of Artemisia species artemetin, casticin, sesartemin and yangambin in addition to coumarins were identified in all extracts. Aqueous extract obtained by infusion exerted the highest radical scavenging and ions reducing properties while that prepared by maceration displayed the highest chelating power. Methanol extracts obtained by the two methods of extraction exerted the highest anti-Tyr activity while that obtained by maceration showed the best α-glucosidase inhibition activity. These findings indicated that A. absinthium is a rich source of bioactive molecules with possible therapeutic applications.
dc.identifier.articlenumbere202400893
dc.identifier.doi10.1002/cbdv.202400893
dc.identifier.eissn1612-1880
dc.identifier.issn1612-1872
dc.identifier.issue8
dc.identifier.pmid38779862
dc.identifier.scopus2-s2.0-85198495649
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/1547
dc.identifier.volume21
dc.identifier.wosWOS:001271253600001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofChemistry and Biodiversity
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectantioxidant
dc.subjectArtemisia absinthium
dc.subjectenzyme inhibition
dc.subjectherbal medicine
dc.subjectphytoconstituents
dc.subject.otheralpha-Glucosidases
dc.subject.otherAntioxidants
dc.subject.otherArtemisia absinthium
dc.subject.otherEnzyme Inhibitors
dc.subject.otherFlavonoids
dc.subject.otherGlycoside Hydrolase Inhibitors
dc.subject.otherPhenols
dc.subject.otherPlant Components, Aerial
dc.subject.otherPlant Extracts
dc.subject.otherSolvents
dc.subject.other2 isopropylmalic acid
dc.subject.other9 hydroxyoctadecadienoic acid
dc.subject.otheracetic acid ethyl ester
dc.subject.otheralpha glucosidase
dc.subject.otherantidiabetic agent
dc.subject.otherantioxidant
dc.subject.otherapigenin
dc.subject.otherartemetin
dc.subject.otherArtemisia absinthium extract
dc.subject.otherasperulosidic acid
dc.subject.otherastragalin
dc.subject.othercaffeic acid
dc.subject.othercasticin
dc.subject.otherchelating agent
dc.subject.otherchlorogenic acid
dc.subject.otherchryptochlorogenic acid
dc.subject.otherchrysoeriol
dc.subject.othercitric acid
dc.subject.othercoumaric acid
dc.subject.othercoumarin derivative
dc.subject.otherdicaffeoylquinic acid isomer 1
dc.subject.otherdicaffeoylquinic acid isomer 2
dc.subject.otherdichloromethane
dc.subject.otherdimethoxyangelicin
dc.subject.otherdimethoxypsoralen
dc.subject.otherdodecanedioic acid
dc.subject.othereupatilin
dc.subject.otherflavonoid
dc.subject.othergentisic acid
dc.subject.otherheraclenin
dc.subject.otherheraclenol
dc.subject.otherhexane
dc.subject.otherhydroxysuberic acid
dc.subject.otherisofraxidin
dc.subject.otherisoimperatorin
dc.subject.otherisoquercetin
dc.subject.otherisorhamnetin 7 o rutinoside
dc.subject.otherkaempferol
dc.subject.otherkynurenic acid
dc.subject.otherlinolenic acid
dc.subject.otherluteolin
dc.subject.othermalic acid
dc.subject.othermalyngic acid
dc.subject.othermetal ion
dc.subject.othermethanol
dc.subject.othermethoxsalen
dc.subject.otherneochlorogenic acid
dc.subject.othernicotiflorin
dc.subject.otherpentosalen
dc.subject.otherphenol derivative
dc.subject.otherpheophytin A
dc.subject.otherpinellic acid
dc.subject.otherpranferol
dc.subject.otherpsoralen
dc.subject.otherpsoralen derivative
dc.subject.otherquercetin
dc.subject.otherquercetin o hexoside
dc.subject.otherquinic acid
dc.subject.otherrosmarinic acid
dc.subject.otherrutoside
dc.subject.othersaccharic acid
dc.subject.otherscavenger (compound)
dc.subject.otherscopoletin
dc.subject.othersesartemin
dc.subject.othersolvent
dc.subject.otherspinacetin 3 o glucoside
dc.subject.otherspinacetin 3 o rutinoside
dc.subject.otherspinacetin o hexoside
dc.subject.othersyringic acid
dc.subject.othertetrahydroxy flavone o rhamnosylhexoside
dc.subject.othertraumatic acid
dc.subject.othertrihydroxy trimethoxy flavone isomer 2
dc.subject.othertrihydroxy trimethoxy iso flavone isomer 1
dc.subject.othertuberonic acid
dc.subject.othertuberonic acid sulfate
dc.subject.otherunclassified drug
dc.subject.otherundecanedioic acid
dc.subject.othervanillic acid
dc.subject.otheryangambin
dc.subject.otherenzyme inhibitor
dc.subject.otherglycosidase inhibitor
dc.subject.otherplant extract
dc.subject.otherAlzheimer disease
dc.subject.otheranalytic method
dc.subject.otherantidiabetic activity
dc.subject.otherantioxidant activity
dc.subject.otherArticle
dc.subject.otherchemical composition
dc.subject.othercontrolled study
dc.subject.otherdiabetes mellitus
dc.titleAnalyzing the Chemical Constituents and In Vitro Biological Effects of Extracts Artemisia absinthium L. Extracts Obtained Using Different Methodologies and Solvents
dc.typeArticle
rdl.citation.openalex3
rdl.citation.scopus2
rdl.departmentDepartment of Botany, Faculty of Science, University of Khartoum, Khartoum, Sudan
rdl.departmentUniversité de Lorraine, INRAE, LAE, F-54000, Nancy, France
rdl.departmentDepartment of Biology, Faculty of Science, Selcuk University, Konya, Turkey
rdl.departmentMunzur University, Tunceli Vocational School, Medical Documentation and Secretaryship Pr., Tunceli, Turkey
rdl.departmentAgricultural and Molecular Research and Service Institute, University of Nyíregyháza, Nyíregyháza, Hungary
rdl.departmentDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131, Padua, Italy
rdl.oa.statusclosed
rdl.scopus.quartileQ3
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED