Study of sample preparation for metabolomic profiling of human saliva by liquid chromatography–time of flight/mass spectrometry

► A metabolite profiling analysis of human saliva by LC–TOF/MS was carried out. ► With this aim, sample preparation was optimized to increase metabolite coverage. ► The resulting method was used to obtain the human salivary metabolome. ► Thus, 168 compounds were identified, including sugars, lipids,...

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Bibliographic Details
Published inJournal of Chromatography A Vol. 1248; pp. 178 - 181
Main Authors Álvarez-Sánchez, B., Priego-Capote, F., Luque de Castro, M.D.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 27.07.2012
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Summary:► A metabolite profiling analysis of human saliva by LC–TOF/MS was carried out. ► With this aim, sample preparation was optimized to increase metabolite coverage. ► The resulting method was used to obtain the human salivary metabolome. ► Thus, 168 compounds were identified, including sugars, lipids, and antioxidants. Saliva has recently gained popularity as a potential tool for diagnosis and biomarkers monitoring, as saliva composition may potentially reflect plasma metabolite levels and, therefore, may be used as an indicator of the physiological state. The aim of the present study was to optimize a sample preparation protocol to obtain a metabolite profiling analysis of human saliva by liquid chromatography–time-of-flight/mass spectrometry (LC–TOF/MS) in high-accuracy mode. Under the optimum sample preparation conditions, identification of potential molecular features was carried out. This resulted in 75 compounds tentatively identified from an acidic extract and 33 from an alkaline extract, with a mass tolerance window below 10ppm. Amino acids, lipids antioxidants and other potentially interesting biomarkers such as polyamines, vitamin B3, and ethylphosphate have been identified. This study covers the gap of knowledge about this biofluid and opens new possibilities for the selection of saliva as source of metabolite biomarkers representative of specific disorders.
Bibliography:http://dx.doi.org/10.1016/j.chroma.2012.05.029
ISSN:0021-9673
1873-3778
DOI:10.1016/j.chroma.2012.05.029