Development, validation and application of LC-MS/MS method for quantification of amino acids, kynurenine and serotonin in human plasma.
Amino Acids
/ blood
Biosensing Techniques
Calibration
Chromatography, High Pressure Liquid
Humans
Kynurenine
/ analysis
Limit of Detection
Linear Models
Reproducibility of Results
Sensitivity and Specificity
Serotonin
/ blood
Solvents
/ chemistry
Spectrometry, Mass, Electrospray Ionization
Tandem Mass Spectrometry
/ methods
Tryptophan
/ metabolism
Amino acid
Fit-for-purpose validation
Kynurenine
LC–MS/MS
Serotonin
Surrogate matrix
Journal
Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336
Informations de publication
Date de publication:
20 Feb 2020
20 Feb 2020
Historique:
received:
16
08
2019
revised:
06
11
2019
accepted:
27
11
2019
pubmed:
19
12
2019
medline:
18
11
2020
entrez:
19
12
2019
Statut:
ppublish
Résumé
Altered serotonergic neurotransmission is a key factor in several neurologic and psychiatric disorders such as migraine. Human and animal studies suggest that chronically low interictal serotonin levels of plasma and brain may facilitate increased activity of the trigeminovascular pathway, and may contribute to development of repeated migraine attacks. However, brain serotonin synthesis is affected by the concentration of tryptophan, its metabolites and a number of amino acids. In this work a simple and robust LC-MS/MS method for the quantitative determination of valine, leucine, isoleucine, phenylalanine, tyrosine, tryptophan, serotonin and kynurenine in human plasma has been developed and validated. Sample preparation was achieved by protein precipitation, using trifluoroacetic acid. Chromatographic separation was carried out on a Supelco Ascentis® Express C18 column (3.0 mm i.d. × 150 mm, 2.7 μm) equipped with an Agilent Zorbax Eclipse XDB C8 guard-column under isocratic conditions at a flow rate of 0.4 mL/min, over a 6.5 min run time. Mobile phase was 0.2% trifluoroacetic acid - acetonitrile (85:15, v/v). The eight analytes and two internal standards were ionized by positive electrospray ionization and detected in multiple reaction monitoring mode. A "fit-for-purpose" validation approach was adopted using surrogate matrix for the preparation of calibration samples. The calibration curves of all analytes showed excellent linearities with a correlation coefficient (r
Identifiants
pubmed: 31851908
pii: S0731-7085(19)31998-3
doi: 10.1016/j.jpba.2019.113018
pii:
doi:
Substances chimiques
Amino Acids
0
Solvents
0
Serotonin
333DO1RDJY
Kynurenine
343-65-7
Tryptophan
8DUH1N11BX
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
113018Informations de copyright
Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest Authors declare no conflict of interest.