Sample pretreatment and extraction method dictate the untargeted lipidomics profile of <i>Fucus vesiculosus</i> detected by ultra-high performance liquid chromatography-mass spectrometry

dc.contributor.authorDing, Cong
dc.contributor.authorFabritius, Mikael
dc.contributor.authorYang, Baoru
dc.contributor.organizationfi=elintarviketieteet|en=Food Sciences|
dc.contributor.organization-code1.2.246.10.2458963.20.15178954341
dc.converis.publication-id523357372
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/523357372
dc.date.accessioned2026-05-15T20:11:38Z
dc.description.abstract<p>Untargeted food lipidomics is increasingly applied in food research. Yet the impact of pretreatment and lipid extraction methods on the lipidomics profiles detected in food matrices has not been systematically characterized. We used the brown macroalgae <i>Fucus vesiculosus</i> as a model to examine how these factors shape the lipid recovery and lipidomic profiles detected using ultra-high performance liquid chromatography-high resolution quadrupole time of flight mass spectrometry (RPLC–QTOF–MS/MS). Within Bligh & Dyer (BD) extraction system, homogenization time, ultrasonication time and extraction cycles significantly altered total lipid yield and the number of detected lipids. Homogenization and ultrasonication as sample pretreatments improved recovery of glycolipids and phospholipids, whereas prolonged treatments led to the loss of highly unsaturated polar lipids. Increasing the water phase in the solvent system had little effect on lipid yield but reduced the number of polar lipid species detected. Under identical pretreatments, BD and Folch extractions yielded similar total numbers of lipid species (∼270) but clearly different class distributions: Folch extraction favoured TG and SQDG, whereas BD extraction enriched MGDG and several betaine-type lipids. These results show that both pretreatment conditions and choice of extraction methods can markedly influence lipid yields, polar lipid coverage, and relative abundance of different lipid classes. Careful design and transparent reporting of extraction protocols are therefore essential for robust and comparable food lipidomics.<br></p>
dc.identifier.eissn2772-5022
dc.identifier.urihttps://www.utupub.fi/handle/11111/60713
dc.identifier.urlhttps://doi.org/10.1016/j.afres.2026.101967
dc.identifier.urnURN:NBN:fi-fe2026051546199
dc.language.isoen
dc.okm.affiliatedauthorDing, Cong
dc.okm.affiliatedauthorFabritius, Mikael
dc.okm.affiliatedauthorYang, Baoru
dc.okm.discipline1182 Biochemistry, cell and molecular biologyen_GB
dc.okm.discipline1182 Biokemia, solu- ja molekyylibiologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier
dc.publisher.countryNetherlandsen_GB
dc.publisher.countryAlankomaatfi_FI
dc.publisher.country-codeNL
dc.relation.articlenumber101967
dc.relation.doi10.1016/j.afres.2026.101967
dc.relation.ispartofjournalApplied Food Research
dc.relation.issue1
dc.relation.volume6
dc.titleSample pretreatment and extraction method dictate the untargeted lipidomics profile of <i>Fucus vesiculosus</i> detected by ultra-high performance liquid chromatography-mass spectrometry
dc.year.issued2026

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