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NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents

Signal stability is essential for reliable multivariate data analysis. Urine samples show strong variance in signal positions due to inter patient differences. Here we study the exchange of the solvent of a defined urine matrix and how it affects signal and integral stability of the urinary metaboli...

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Detalles Bibliográficos
Autores principales: Görling, Benjamin, Bräse, Stefan, Luy, Burkhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041126/
https://www.ncbi.nlm.nih.gov/pubmed/27598217
http://dx.doi.org/10.3390/metabo6030027
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author Görling, Benjamin
Bräse, Stefan
Luy, Burkhard
author_facet Görling, Benjamin
Bräse, Stefan
Luy, Burkhard
author_sort Görling, Benjamin
collection PubMed
description Signal stability is essential for reliable multivariate data analysis. Urine samples show strong variance in signal positions due to inter patient differences. Here we study the exchange of the solvent of a defined urine matrix and how it affects signal and integral stability of the urinary metabolites by NMR spectroscopy. The exchange solvents were methanol, acetonitrile, dimethyl sulfoxide, chloroform, acetone, dichloromethane, and dimethyl formamide. Some of these solvents showed promising results with a single batch of urine. To evaluate further differences between urine samples, various acid, base, and salt solutions were added in a defined way mimicking to some extent inter human differences. Corresponding chemical shift changes were monitored.
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spelling pubmed-50411262016-10-05 NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents Görling, Benjamin Bräse, Stefan Luy, Burkhard Metabolites Article Signal stability is essential for reliable multivariate data analysis. Urine samples show strong variance in signal positions due to inter patient differences. Here we study the exchange of the solvent of a defined urine matrix and how it affects signal and integral stability of the urinary metabolites by NMR spectroscopy. The exchange solvents were methanol, acetonitrile, dimethyl sulfoxide, chloroform, acetone, dichloromethane, and dimethyl formamide. Some of these solvents showed promising results with a single batch of urine. To evaluate further differences between urine samples, various acid, base, and salt solutions were added in a defined way mimicking to some extent inter human differences. Corresponding chemical shift changes were monitored. MDPI 2016-09-02 /pmc/articles/PMC5041126/ /pubmed/27598217 http://dx.doi.org/10.3390/metabo6030027 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Görling, Benjamin
Bräse, Stefan
Luy, Burkhard
NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents
title NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents
title_full NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents
title_fullStr NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents
title_full_unstemmed NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents
title_short NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents
title_sort nmr chemical shift ranges of urine metabolites in various organic solvents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041126/
https://www.ncbi.nlm.nih.gov/pubmed/27598217
http://dx.doi.org/10.3390/metabo6030027
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