NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents

被引:5
|
作者
Goerling, Benjamin [1 ,2 ]
Braese, Stefan [1 ,3 ]
Luy, Burkhard [1 ,2 ]
机构
[1] Karlsruhe Inst Technol, Inst Organ Chem, Fritz Haber Weg 6, D-76131 Karlsruhe, Germany
[2] Karlsruhe Inst Technol, Inst Biol Interfaces Magnet Resonance 4, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[3] Karlsruhe Inst Technol, Inst Toxicol & Genet, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
关键词
NMR spectroscopy; urine; solvents; methanol; DMSO; H-1-NMR SPECTROSCOPY; SAMPLE PREPARATION; METABONOMICS;
D O I
10.3390/metabo6030027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:8
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