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dc.contributor.authorSan Nicolas Oruetxebarria, Markel
dc.contributor.authorVillate Uribe, Aitor
dc.contributor.authorOlivares Zabalandicoechea, Maitane
dc.contributor.authorEtxebarria Loizate, Nestor
dc.contributor.authorZuloaga Zubieta, Olatz
dc.contributor.authorAizpurua Olaizola, Oier
dc.contributor.authorUsobiaga Epelde, Aresatz ORCID
dc.date.accessioned2023-12-26T10:05:33Z
dc.date.available2023-12-26T10:05:33Z
dc.date.issued2023-10
dc.identifier.citationAnalytica Chimica Acta 1279 : (2023) // Article ID 341848es_ES
dc.identifier.issn0003-2670
dc.identifier.issn1873-4324
dc.identifier.urihttp://hdl.handle.net/10810/63633
dc.description.abstractBackground Recent increase in public acceptance of cannabis as a natural medical alternative for certain neurological pathologies has led to its approval in different regions of the world. However, due to its previous illegal background, little research has been conducted around its biochemical insights. Therefore, in the current framework, metabolomics may be a suitable approach for deepening the knowledge around this plant species. Nevertheless, experimental methods in metabolomics must be carefully handled, as slight modifications can lead to metabolomic coverage loss. Hence, the main objective of this work was to optimise an analytical method for appropriate untargeted metabolomic screening of cannabis. Results We present an empirically optimised experimental procedure through which the broadest metabolomic coverage was obtained, in which extraction solvents for metabolite isolation, chromatographic columns for LC-qOrbitrap analysis and plant-representative biological tissues were compared. By exploratory means, it was determined that the solvent combination composed of CHCl3:H2O:CH3OH (2:1:1, v/v) provided the highest number of features from diverse chemical classes, as it was a two-phase extractant. In addition, a reverse phase 2.6 μm C18 100 Å (150 × 3 mm) chromatographic column was determined as the appropriate choice for adequate separation and further detection of the diverse metabolite classes. Apart from that, overall chromatographic peak quality provided by each column was observed and the need for batch correction methods through quality control (QC) samples was confirmed. At last, leaf and flower tissues resulted to provide complementary metabolic information of the plant, to the detriment of stem tissue, which resulted to be negligible. Significance It was concluded that the optimised experimental procedure could significantly ease the path for future research works related to cannabis metabolomics by LC-HRMS means, as the work was based on previous plant metabolomics literature. Furthermore, it is crucial to highlight that an optimal analytical method can vary depending on the main objective of the research, as changes in the experimental factors can lead to different outcomes, regardless of whether the results are better or worse.es_ES
dc.description.sponsorshipThis work was financially supported by the Education Department of the Basque Country as a consolidated group of the Basque Research System (IT1213-19) and by Sovereign Fields S.L., in the framework of the project Metabolomic study of Cannabis Sativa L. cultivations and determination of contaminants in medical cannabis plants.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectplant metabolomicses_ES
dc.subjectexperimental factorses_ES
dc.subjectCannabis sativa L.es_ES
dc.subjectLC-HRMSes_ES
dc.subjectmetabolomic coveragees_ES
dc.subjectdata mininges_ES
dc.titleExploratory optimisation of a LC-HRMS based analytical method for untargeted metabolomic screening of Cannabis Sativa L. through Data Mininges_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by- nc-nd/4.0/).es_ES
dc.rights.holderAtribución-NoComercial-SinDerivadas 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0003267023010693es_ES
dc.identifier.doi10.1016/j.aca.2023.341848
dc.departamentoesQuímica analíticaes_ES
dc.departamentoeuKimika analitikoaes_ES


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© 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-
nc-nd/4.0/).
Except where otherwise noted, this item's license is described as © 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by- nc-nd/4.0/).