Comparison of tetrahydrofuran and ethyl acetate as extraction solvents for urinary organic acid analysis

Gy Wittmann, E. Karg, A. Mühl, O. A. Bodamer, S. Türi

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The analysis of urinary organic acids is crucial for the diagnosis of many inborn errors of metabolism. A vital part of the analytical process is the extraction procedure. The sensitivity and linearity of the analysis of 26 diagnostically important urinary metabolites with tetrahydrofuran (THF) and ethyl acetate (EtOAc) as extraction solvents were determined by gas chromatography-mass spectrometry. Good linearity (r2>0.90) was observed for all of the compounds in the investigated concentration range (290-900 μmol/L) for both solvents. For less polar compounds, THF extraction yielded lower or similar sensitivities as compared with EtOAc (sensitivity ratio: 0.6-1.3). For more polar compounds, however, much higher sensitivities were observed when THF was used (sensitivity ratio: 1.8-17.2). Our results provide information concerning the use of THF for the sensitive quantitative analysis of polar urinary metabolites which are difficult to quantify using EtOAc.

Original languageEnglish
Pages (from-to)73-80
Number of pages8
JournalJournal of Inherited Metabolic Disease
Volume31
Issue number1
DOIs
StatePublished - Feb 1 2008

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Acids
Inborn Errors Metabolism
Gas Chromatography-Mass Spectrometry
ethyl acetate
tetrahydrofuran

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics
  • Endocrinology

Cite this

Comparison of tetrahydrofuran and ethyl acetate as extraction solvents for urinary organic acid analysis. / Wittmann, Gy; Karg, E.; Mühl, A.; Bodamer, O. A.; Türi, S.

In: Journal of Inherited Metabolic Disease, Vol. 31, No. 1, 01.02.2008, p. 73-80.

Research output: Contribution to journalArticle

Wittmann, Gy ; Karg, E. ; Mühl, A. ; Bodamer, O. A. ; Türi, S. / Comparison of tetrahydrofuran and ethyl acetate as extraction solvents for urinary organic acid analysis. In: Journal of Inherited Metabolic Disease. 2008 ; Vol. 31, No. 1. pp. 73-80.
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