Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/45299
Full metadata record
DC FieldValueLanguage
dc.contributor.authorZarate, E-
dc.contributor.authorBoyle, V-
dc.contributor.authorRupprecht, U-
dc.contributor.authorGreen, S-
dc.contributor.authorVillas-Boas, S-
dc.contributor.authorBaker, P-
dc.contributor.authorPinu, F-
dc.date.accessioned2019-08-20T14:23:12Z-
dc.date.available2019-08-20T14:23:12Z-
dc.date.issued2016-12-29-
dc.identifier.citationMetabolites, 2017, 7 (1), pp. 1-1en
dc.identifier.urihttp://hdl.handle.net/2381/45299-
dc.description.abstractGas Chromatography-Mass Spectrometry (GC-MS) has long been used for metabolite profiling of a wide range of biological samples. Many derivatisation protocols are already available and among these, trimethylsilyl (TMS) derivatisation is one of the most widely used in metabolomics. However, most TMS methods rely on off-line derivatisation prior to GC-MS analysis. In the case of manual off-line TMS derivatisation, the derivative created is unstable, so reduction in recoveries occurs over time. Thus, derivatisation is carried out in small batches. Here, we present a fully automated TMS derivatisation protocol using robotic autosamplers and we also evaluate a commercial software, Maestro available from Gerstel GmbH. Because of automation, there was no waiting time of derivatised samples on the autosamplers, thus reducing degradation of unstable metabolites. Moreover, this method allowed us to overlap samples and improved throughputs. We compared data obtained from both manual and automated TMS methods performed on three different matrices, including standard mix, wine, and plasma samples. The automated TMS method showed better reproducibility and higher peak intensity for most of the identified metabolites than the manual derivatisation method. We also validated the automated method using 114 quality control plasma samples. Additionally, we showed that this online method was highly reproducible for most of the metabolites detected and identified (RSD < 20) and specifically achieved excellent results for sugars, sugar alcohols, and some organic acids. To the very best of our knowledge, this is the first time that the automated TMS method has been applied to analyse a large number of complex plasma samples. Furthermore, we found that this method was highly applicable for routine metabolite profiling (both targeted and untargeted) in any metabolomics laboratoryen
dc.description.sponsorshipNew Zealand Agriculture and Marketing Research and Development Trust (AGMARDT)en
dc.language.isoenen
dc.publisherMDPIen
dc.rightsCopyright © the authors, 2016. This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subjectmetabolomicsen
dc.subjectmatrixen
dc.subjectautomationen
dc.subjectsample preparationen
dc.subjectsugarsen
dc.subjectamino acidsen
dc.subjectorganic acidsen
dc.titleFully Automated Trimethylsilyl (TMS) Derivatisation Protocol for Metabolite Profiling by GC-MSen
dc.typeJournal Articleen
dc.identifier.doi10.3390/metabo7010001-
dc.identifier.eissn2218-1989-
dc.description.statusPeer-revieweden
dc.description.versionPublisher Versionen
pubs.organisational-group/Organisationen
pubs.organisational-group/Organisation/COLLEGE OF LIFE SCIENCESen
dc.dateaccepted2016-12-26-
Appears in Collections:Published Articles, Dept. of Health Sciences

Files in This Item:
File Description SizeFormat 
metabolites-07-00001.pdfPublished (publisher PDF)14.28 MBAdobe PDFView/Open


Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.