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Impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies
INTRODUCTION: Untargeted metabolomics intends to objectively analyze a wide variety of compounds. Their diverse physicochemical properties make it difficult to choose an appropriate reconstitution solvent after sample evaporation without influencing the chromatography or hamper column sorbent integr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052028/ https://www.ncbi.nlm.nih.gov/pubmed/32124055 http://dx.doi.org/10.1007/s11306-019-1631-1 |
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author | Manier, Sascha K. Meyer, Markus R. |
author_facet | Manier, Sascha K. Meyer, Markus R. |
author_sort | Manier, Sascha K. |
collection | PubMed |
description | INTRODUCTION: Untargeted metabolomics intends to objectively analyze a wide variety of compounds. Their diverse physicochemical properties make it difficult to choose an appropriate reconstitution solvent after sample evaporation without influencing the chromatography or hamper column sorbent integrity. OBJECTIVES: The study aimed to identify the most appropriate reconstitution solvent for blood plasma samples in terms of feature recovery, four endogenous compounds, and one selected internal standard. METHODS: We investigated several reconstitution solvent mixtures containing acetonitrile and methanol to resolve human plasma extract and evaluated them concerning the peak areas of tryptophan-d(5), glucose, creatinine, palmitic acid, and the phophatidylcholine PC(P-16:0/P-16:0), as well as the total feature count RESULTS: Results indicated that acetonitrile containing 30% methanol was best suited to match all tested criteria at least for human blood plasma samples. CONCLUSION: Despite identifying the mixture of acetonitrile and methanol being suitable as solvent for human blood plasma extracts, we recommend to systematically test for an appropriate reconstitution solvent for each analyzed biomatrix. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11306-019-1631-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7052028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-70520282020-03-16 Impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies Manier, Sascha K. Meyer, Markus R. Metabolomics Short Communication INTRODUCTION: Untargeted metabolomics intends to objectively analyze a wide variety of compounds. Their diverse physicochemical properties make it difficult to choose an appropriate reconstitution solvent after sample evaporation without influencing the chromatography or hamper column sorbent integrity. OBJECTIVES: The study aimed to identify the most appropriate reconstitution solvent for blood plasma samples in terms of feature recovery, four endogenous compounds, and one selected internal standard. METHODS: We investigated several reconstitution solvent mixtures containing acetonitrile and methanol to resolve human plasma extract and evaluated them concerning the peak areas of tryptophan-d(5), glucose, creatinine, palmitic acid, and the phophatidylcholine PC(P-16:0/P-16:0), as well as the total feature count RESULTS: Results indicated that acetonitrile containing 30% methanol was best suited to match all tested criteria at least for human blood plasma samples. CONCLUSION: Despite identifying the mixture of acetonitrile and methanol being suitable as solvent for human blood plasma extracts, we recommend to systematically test for an appropriate reconstitution solvent for each analyzed biomatrix. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11306-019-1631-1) contains supplementary material, which is available to authorized users. Springer US 2020-03-02 2020 /pmc/articles/PMC7052028/ /pubmed/32124055 http://dx.doi.org/10.1007/s11306-019-1631-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Short Communication Manier, Sascha K. Meyer, Markus R. Impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies |
title | Impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies |
title_full | Impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies |
title_fullStr | Impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies |
title_full_unstemmed | Impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies |
title_short | Impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies |
title_sort | impact of the used solvent on the reconstitution efficiency of evaporated biosamples for untargeted metabolomics studies |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052028/ https://www.ncbi.nlm.nih.gov/pubmed/32124055 http://dx.doi.org/10.1007/s11306-019-1631-1 |
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