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Título
Non-separative method based on a single quadrupole mass spectrometer for the semi-quantitative determination of amino acids in saliva samples. A preliminary study
Autor(es)
Palabras clave
Amino acids
Derivatisation reaction
Liquid-liquid extraction
Non-separative method
Partial-least squares regression
Saliva samples
Fecha de publicación
2020
Editor
Elsevier
Citación
Patricia Martín Santos, Miguel del Nogal Sánchez, José Luis Pérez Pavón, Bernardo Moreno Cordero, Non-separative method based on a single quadrupole mass spectrometer for the semi-quantitative determination of amino acids in saliva samples. A preliminary study, Talanta, Volume 208, 2020, 120381, ISSN 0039-9140, https://doi.org/10.1016/j.talanta.2019.120381. (https://www.sciencedirect.com/science/article/pii/S0039914019310148)
Resumen
[EN]Amino acids have been of great interest in clinical studies since variation in their concentration may provide information about different disorders. For the first time, a non-separative method based on single quadrupole mass spectrometry (qMS) for the simultaneous semiquantitative determination of sixteen amino acids in saliva samples has been developed. The method includes derivatisation of amino acids with ethyl chloroformate-pyridine-ethanol to obtain volatile products, liquid-liquid extraction (LLE) and further analysis using a programmed temperature vaporizer (PTV) coupled to qMS. This method could be applied to the analysis of a great number of saliva samples, limiting the use of separative methods only when abnormal concentrations of amino acids were found, reducing analysis time and cost. The results obtained in the determination of amino acids using the non-separative method were compared to those obtained when a separative method based on gas chromatography (GC) was used, providing values of average relative predictive error (E %) ranging between 2 and 48%. Repeatability and reproducibility were tested, obtaining relative standard deviation (RSD) values equal to or lower than 11% and 16%, respectively. Detection limits were in the range of 0.076–8.747 mg L−1 for the non-separative method.
URI
ISSN
0039-9140
DOI
10.1016/j.talanta.2019.120381
Versión del editor
Aparece en las colecciones
- DQANB. Artículos [108]
Patrocinador
P. Martín Santos wishes to thank the University of Salamanca for a predoctoral fellowship
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