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Dried blood spots in clinical lipidomics: optimization and recent findings

dc.contributor.authorFerreira, Helena Beatriz 
dc.contributor.authorGuerra, Inês M. S. 
dc.contributor.authorMelo, Tânia 
dc.contributor.authorRocha, Hugo
dc.contributor.authorMoreira, Ana S. P. 
dc.contributor.authorPaiva, Artur 
dc.contributor.authorDomingues, M. Rosário 
dc.date.accessioned2023-02-03T13:34:00Z
dc.date.available2023-02-03T13:34:00Z
dc.date.issued2022
dc.description.abstractDried blood spots (DBS) are being considered as an alternative sampling method of blood collection that can be used in combination with lipidomic and other omic analysis. DBS are successfully used in the clinical context to collect samples for newborn screening for the measurement of specifc fatty acid derivatives, such as acylcarnitines, and lipids from whole blood for diagnostic purposes. However, DBS are scarcely used for lipidomic analysis and investigations. Lipidomic stud ies using DBS are starting to emerge as a powerful method for sampling and storage in clinical lipidomic analysis, but the major research work is being done in the pre- and analytical steps and procedures, and few in clinical applications. This review presents a description of the impact factors and variables that can afect DBS lipidomic analysis, such as the type of DBS card, haematocrit, homogeneity of the blood drop, matrix/chromatographic efects, and the chemical and physi cal properties of the analyte. Additionally, a brief overview of lipidomic studies using DBS to unveil their application in clinical scenarios is also presented, considering the studies of method development and validation and, to a less extent, for clinical diagnosis using clinical lipidomics. DBS combined with lipidomic approaches proved to be as efective as whole blood samples, achieving high levels of sensitivity and specifcity during MS and MS/MS analysis, which could be a useful tool for biomarker identifcation. Lipidomic profling using MS/MS platforms enables signifcant insights into physiological changes, which could be useful in precision medicine.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationFerreira, H. B., Guerra, I. M. S., Melo, T., Rocha, H., Moreira, A. S. P., Paiva, A., & Domingues, M. R. (2022). Dried blood spots in clinical lipidomics: Optimization and recent findings. Analytical and Bioanalytical Chemistry, 414(24), 7085–7101. https://doi.org/10.1007/s00216-022-04221-1pt_PT
dc.identifier.doi10.1007/s00216-022-04221-1pt_PT
dc.identifier.eissn1618-2650
dc.identifier.issn1618-2642
dc.identifier.urihttp://hdl.handle.net/10400.22/22143
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSpringerpt_PT
dc.relation.publisherversionhttps://link.springer.com/article/10.1007/s00216-022-04221-1pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectDried blood spotspt_PT
dc.subjectMass spectrometrypt_PT
dc.subjectLipidomicspt_PT
dc.subjectDisease biomarkerspt_PT
dc.titleDried blood spots in clinical lipidomics: optimization and recent findingspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage7101pt_PT
oaire.citation.startPage7085pt_PT
oaire.citation.titleAnalytical and Bioanalytical Chemistrypt_PT
oaire.citation.volume414pt_PT
person.familyNameCarvalho de Azevedo Rocha
person.givenNameHugo Daniel
person.identifier.ciencia-id331F-6236-B34F
person.identifier.orcid0000-0001-5447-615X
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationa67d8ec6-bfd4-415f-9615-8d8c8a48166e
relation.isAuthorOfPublication.latestForDiscoverya67d8ec6-bfd4-415f-9615-8d8c8a48166e

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