Quantification of Gluten Exorphin A5 in cerebrospinal fluid by liquid chromatography-mass spectrometry.

J Chromatogr B Analyt Technol Biomed Life Sci

Dipartimento-Struttura Clinica Medica-Patologia Speciale Medica, Istituto di Clinica Medica, University of Sassari, Viale San Pietro 8, 07100 Sassari, Italy.

Published: April 2006

AI Article Synopsis

  • A new method was developed for quantifying Gluten Exorphin A5 (GE-A5) in cerebrospinal fluid (CSF) using liquid chromatography-mass spectrometry (LC-MS).
  • The assay reliably detects GE-A5 with limits of detection at 0.60 ng/mL and quantification at 1.50 ng/mL, showing high accuracy and precision (<5% relative standard deviation).
  • This technique requires minimal CSF volume, making it applicable for studying both small and large animal models.

Article Abstract

In the present work, for the first time, a method for the quantification of the alimentary opioid peptide Gluten Exorphin A5 (GE-A5; Gly-Tyr-Tyr-Pro-Thr) in cerebrospinal fluid (CSF) was developed. Aliquots (5 microL) of CSF were injected into a liquid chromatography-mass spectrometry (LC-MS) instrument equipped with a reversed-phase C18 column at a flow-rate of 0.4 mL/min. The mobile phase consisted of Eluent A water with 0.6% acetic acid as an ion-pairing reagent and Eluent B acetonitrile/methanol (75:25, v/v). The LC-MS system was programmed to divert column flow to waste for 4 min after injection, after which time flow was directed into the mass spectrometer that operated in positive ion mode. No significant interfering peaks were detected at the retention times of GE-A5 in CSF blanks. The lower limit of detection and the lower limit of quantitation values for GE-A5 in CSF were established at 0.60 and 1.50 ng/mL, respectively. The intra- and inter-day precision values were <5% relative standard deviation. The intra- and inter-day accuracy were 99.6-102.8% and 100.0-101.9%, respectively. The reported assay employs extremely small volumes of CSF, thus allowing the analysis of GE-A5 from both small and large animal models.

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Source
http://dx.doi.org/10.1016/j.jchromb.2006.01.038DOI Listing

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