The capabilities of atmospheric pressure chemical ionization liquid chromatography/mass spectrometry (APCI-LC/MS) were investigated for the analysis of urinary 2,5-hexanedione (2,5-HD) and for the identification and characterization of other n-hexane Phase I metabolites in hydrolized urine samples. Chromatography was performed under reversed phase conditions at 0.75 mL minÿ1 flow rate. The ionization of 2,5-HD and other n-hexane metabolites was obtained in positive ion mode. After optimization of several interface parameters, the linearity, sensitivity and precision of the method were determined operating in the selected ion monitoring mode. Detection limits were 0.02 and 0.05 mg Lÿ1 in water and urine respectively, with linear calibration curves in the 0.05–10 mg Lÿ1 concentration range. Repeatability and both intra-day and inter-day precision were determined at two concentration levels (0.5 and 5.0 mg Lÿ1), and relative standard deviations were in the 1.3%–5.3% range. The method was applied to the quantitative analysis of 2,5-HD in urine samples from an external Quality Assurance Programme for Organic Solvent Metabolites. Moreover, the metabolites 5-hydroxy-2-hexanone, 2,5-hexanediol and 4,5- dihydroxy-2-hexanone were identified and confirmed in hydrolyzed urine of rats exposed to n-hexane.

Determination of n-Hexane Metabolites byLiquid Chromatography/Mass Spectrometry 1.2,5-Hexanedione and Other Phase I Metabolitesin Untreated and Hydrolyzed Urine Samples byAtmospheric Pressure Chemical Ionization / Andreoli, Roberta; Paola, Manini; Mutti, Antonio; Bergamaschi, Enrico; Wilfried M. A., Niessen. - In: RAPID COMMUNICATIONS IN MASS SPECTROMETRY. - ISSN 0951-4198. - 12:(1998), pp. 1410-1416.

Determination of n-Hexane Metabolites byLiquid Chromatography/Mass Spectrometry 1.2,5-Hexanedione and Other Phase I Metabolitesin Untreated and Hydrolyzed Urine Samples byAtmospheric Pressure Chemical Ionization

ANDREOLI, Roberta;MUTTI, Antonio;BERGAMASCHI, Enrico;
1998-01-01

Abstract

The capabilities of atmospheric pressure chemical ionization liquid chromatography/mass spectrometry (APCI-LC/MS) were investigated for the analysis of urinary 2,5-hexanedione (2,5-HD) and for the identification and characterization of other n-hexane Phase I metabolites in hydrolized urine samples. Chromatography was performed under reversed phase conditions at 0.75 mL minÿ1 flow rate. The ionization of 2,5-HD and other n-hexane metabolites was obtained in positive ion mode. After optimization of several interface parameters, the linearity, sensitivity and precision of the method were determined operating in the selected ion monitoring mode. Detection limits were 0.02 and 0.05 mg Lÿ1 in water and urine respectively, with linear calibration curves in the 0.05–10 mg Lÿ1 concentration range. Repeatability and both intra-day and inter-day precision were determined at two concentration levels (0.5 and 5.0 mg Lÿ1), and relative standard deviations were in the 1.3%–5.3% range. The method was applied to the quantitative analysis of 2,5-HD in urine samples from an external Quality Assurance Programme for Organic Solvent Metabolites. Moreover, the metabolites 5-hydroxy-2-hexanone, 2,5-hexanediol and 4,5- dihydroxy-2-hexanone were identified and confirmed in hydrolyzed urine of rats exposed to n-hexane.
1998
Determination of n-Hexane Metabolites byLiquid Chromatography/Mass Spectrometry 1.2,5-Hexanedione and Other Phase I Metabolitesin Untreated and Hydrolyzed Urine Samples byAtmospheric Pressure Chemical Ionization / Andreoli, Roberta; Paola, Manini; Mutti, Antonio; Bergamaschi, Enrico; Wilfried M. A., Niessen. - In: RAPID COMMUNICATIONS IN MASS SPECTROMETRY. - ISSN 0951-4198. - 12:(1998), pp. 1410-1416.
File in questo prodotto:
File Dimensione Formato  
Hexane metabolite 1 2,5HD Andreoli RCMS 1998.pdf

non disponibili

Tipologia: Documento in Post-print
Licenza: Creative commons
Dimensione 137.47 kB
Formato Adobe PDF
137.47 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2433792
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 11
  • ???jsp.display-item.citation.isi??? ND
social impact