Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/36920
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dc.contributor.authorFernandes, Sara R.pt_PT
dc.contributor.authorBarreiros, Luisapt_PT
dc.contributor.authorOliveira, Rita F.pt_PT
dc.contributor.authorCruz, Agostinhopt_PT
dc.contributor.authorPrudêncio, Cristinapt_PT
dc.contributor.authorOliveira, Ana Isabelpt_PT
dc.contributor.authorPinho, Cláudiapt_PT
dc.contributor.authorSantos, Nunopt_PT
dc.contributor.authorMorgado, Joaquimpt_PT
dc.date.accessioned2023-04-06T15:39:35Z-
dc.date.available2023-04-06T15:39:35Z-
dc.date.issued2019-04-
dc.identifier.issn0367-326Xpt_PT
dc.identifier.urihttp://hdl.handle.net/10773/36920-
dc.description.abstractAzadirachta indica A. Juss. (Neem) is an Indian tree recognized for its activity as pesticide, as well as several pharmacological properties. Among the various compounds already isolated and studied from Neem tree, azadirachtin (AZA) was identified as the main bioactive compound. Azadirachtin can be found at different parts of the Neem plant but assumes its maximum concentration at the seed level. This compound features a quite complex chemical structure, which justifies the 20-plus-year difficulty to identify the synthetic pathway that subsequently permitted to carry out its artificial synthesis. Azadirachtin is widely used as a basis for production of biopesticides; nevertheless, other properties have been recognized for this substance, among which the anticancer and antimalarial activity stand out. The methods available for azadirachtin extraction are diverse, including solid-liquid extraction and extraction with solvents at high or low temperatures. Alcohol based solvents are associated with higher extraction yields and are therefore preferred for the isolation of azadirachtin from plant parts. Clean-up of the extracts is generally required for further purification. The highest azadirachtin levels have been obtained from Neem seeds but concentration values present a large variation between batches. Therefore, in addition to extraction procedures, it is essential to establish routine methods for azadirachtin identification and quantification. Chromatography-based techniques are preferably selected for detection and quantification of azadirachtin in plant matrices. Overall, this process will guarantee a future reproducible, safe and effective use of the extracts in formulations for commercial applications.pt_PT
dc.language.isoengpt_PT
dc.publisherElsevierpt_PT
dc.relationPT2020 UID/QUI/50006/2013pt_PT
dc.relationPOCI/01/0145/FEDER/007265pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH%2FBD%2F130948%2F2017/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/FARH/SFRH%2FBPD%2F89668%2F2012/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectAzadirachta indicapt_PT
dc.subjectNeempt_PT
dc.subjectBioactive compoundspt_PT
dc.subjectChemical characterizationpt_PT
dc.subjectExtractionpt_PT
dc.subjectQuantificationpt_PT
dc.titleChemistry, bioactivities, extraction and analysis of azadirachtin: state-of-the-artpt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage141pt_PT
degois.publication.lastPage150pt_PT
degois.publication.titleFitoterapiapt_PT
degois.publication.volume134pt_PT
dc.identifier.doi10.1016/j.fitote.2019.02.006pt_PT
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