Tissue storage affects lipidome profiling in comparison to in vivo microsampling approach

Abstract Low-invasive in vivo solid-phase microextraction (SPME) was used to investigate the lipid profiles of muscle tissue of living fish. Briefly, mixed mode SPME fibers were inserted into the muscle for 20 min extraction, and then the fibers were desorbed in an optimal mixture of solvents. The o...

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Main Authors: Anna Roszkowska, Miao Yu, Vincent Bessonneau, Leslie Bragg, Mark Servos, Janusz Pawliszyn
Format: Article
Language:English
Published: Nature Publishing Group 2018-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-018-25428-2
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spelling doaj-b929cd0fe14c447f8692b54e6e94e8a42020-12-08T04:35:10ZengNature Publishing GroupScientific Reports2045-23222018-05-018111010.1038/s41598-018-25428-2Tissue storage affects lipidome profiling in comparison to in vivo microsampling approachAnna Roszkowska0Miao Yu1Vincent Bessonneau2Leslie Bragg3Mark Servos4Janusz Pawliszyn5Department of Chemistry, University of WaterlooDepartment of Chemistry, University of WaterlooDepartment of Chemistry, University of WaterlooDepartment of Biology, University of WaterlooDepartment of Biology, University of WaterlooDepartment of Chemistry, University of WaterlooAbstract Low-invasive in vivo solid-phase microextraction (SPME) was used to investigate the lipid profiles of muscle tissue of living fish. Briefly, mixed mode SPME fibers were inserted into the muscle for 20 min extraction, and then the fibers were desorbed in an optimal mixture of solvents. The obtained lipid profile was then compared and contrasted to that obtained with employment of ex vivo SPME and solid-liquid extraction (SLE) from fish muscle tissue belonging to the same group of fish, following a one-year storage period. Ex vivo SPME analysis of stored muscle samples revealed 10-fold decrease in the number of detected molecular features in comparison to in vivo study. Moreover, in vivo microsampling enabled the identification of different classes of bioactive lipids, including fatty acyls, not present in the lipid profile obtained through ex vivo SPME and SLE, suggesting the alterations occurring in the unbound lipid fraction of the system under study during the storage and also indicating the advantage of the in vivo extraction approach.https://doi.org/10.1038/s41598-018-25428-2
collection DOAJ
language English
format Article
sources DOAJ
author Anna Roszkowska
Miao Yu
Vincent Bessonneau
Leslie Bragg
Mark Servos
Janusz Pawliszyn
spellingShingle Anna Roszkowska
Miao Yu
Vincent Bessonneau
Leslie Bragg
Mark Servos
Janusz Pawliszyn
Tissue storage affects lipidome profiling in comparison to in vivo microsampling approach
Scientific Reports
author_facet Anna Roszkowska
Miao Yu
Vincent Bessonneau
Leslie Bragg
Mark Servos
Janusz Pawliszyn
author_sort Anna Roszkowska
title Tissue storage affects lipidome profiling in comparison to in vivo microsampling approach
title_short Tissue storage affects lipidome profiling in comparison to in vivo microsampling approach
title_full Tissue storage affects lipidome profiling in comparison to in vivo microsampling approach
title_fullStr Tissue storage affects lipidome profiling in comparison to in vivo microsampling approach
title_full_unstemmed Tissue storage affects lipidome profiling in comparison to in vivo microsampling approach
title_sort tissue storage affects lipidome profiling in comparison to in vivo microsampling approach
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2018-05-01
description Abstract Low-invasive in vivo solid-phase microextraction (SPME) was used to investigate the lipid profiles of muscle tissue of living fish. Briefly, mixed mode SPME fibers were inserted into the muscle for 20 min extraction, and then the fibers were desorbed in an optimal mixture of solvents. The obtained lipid profile was then compared and contrasted to that obtained with employment of ex vivo SPME and solid-liquid extraction (SLE) from fish muscle tissue belonging to the same group of fish, following a one-year storage period. Ex vivo SPME analysis of stored muscle samples revealed 10-fold decrease in the number of detected molecular features in comparison to in vivo study. Moreover, in vivo microsampling enabled the identification of different classes of bioactive lipids, including fatty acyls, not present in the lipid profile obtained through ex vivo SPME and SLE, suggesting the alterations occurring in the unbound lipid fraction of the system under study during the storage and also indicating the advantage of the in vivo extraction approach.
url https://doi.org/10.1038/s41598-018-25428-2
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