• Medientyp: E-Artikel
  • Titel: Validation of an LC-MS/MS Method for Urinary Lactulose and Mannitol Quantification: Results in Patients with Irritable Bowel Syndrome
  • Beteiligte: Gervasoni, Jacopo; Schiattarella, Arcangelo; Giorgio, Valentina; Primiano, Aniello; Russo, Consuelo; Tesori, Valentina; Scaldaferri, Franco; Urbani, Andrea; Zuppi, Cecilia; Persichilli, Silvia
  • Erschienen: Hindawi Limited, 2016
  • Erschienen in: Disease Markers
  • Sprache: Englisch
  • DOI: 10.1155/2016/5340386
  • ISSN: 0278-0240; 1875-8630
  • Schlagwörter: Biochemistry (medical) ; Clinical Biochemistry ; Genetics ; Molecular Biology ; General Medicine
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  • Beschreibung: <jats:p><jats:italic>Aim</jats:italic>. Lactulose/mannitol ratio is used to assess intestinal barrier function. Aim of this work was to develop a robust and rapid method for the analysis of lactulose and mannitol in urine by liquid chromatography coupled to tandem mass spectrometry. Lactulose/mannitol ratio has been measured in pediatric patients suffering from irritable bowel syndrome.<jats:italic>Methods</jats:italic>. Calibration curves and raffinose, used as internal standard, were prepared in water : acetonitrile 20 : 80. Fifty<jats:italic>μ</jats:italic>L of urine sample was added to 450 <jats:italic>μ</jats:italic>L of internal standard solution. The chromatographic separation was performed using a Luna NH<jats:sub>2</jats:sub>column operating at a flow rate of 200 <jats:italic>μ</jats:italic>L/min and eluted with a linear gradient from 20% to 80% water in acetonitrile. Total run time is 9 minutes. The mass spectrometry operates in electrospray negative mode. Method was fully validated according to European Medicine Agency guidelines.<jats:italic>Results and Conclusions</jats:italic>. Linearity ranged from 10 to 1000 mg/L for mannitol and 2.5 to 1000 mg/L for lactulose. Imprecision in intra- and interassay was lower than 15% for both analytes. Accuracy was higher than 85%. Lactulose/mannitol ratio in pediatric patients is significantly higher than that measured in controls. The presented method, rapid and sensitive, is suitable in a clinical laboratory.</jats:p>
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