Targeted metabolomics in cultured cells and tissues by mass spectrometry: Method development and validation

[Display omitted] •This study introduce a valid bioanalytical method for metabolic profiling.•The method validation and stability were studied carefully based on USFDA guidelines.•The targeted metabolomics method was tested on couple of biological systems cell lines and mouse tissue. Metabolomics is...

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Veröffentlicht in:Analytica chimica acta 2014-10, Vol.845, p.53-61
Hauptverfasser: Abdel Rahman, Anas M., Pawling, Judy, Ryczko, Michael, Caudy, Amy A., Dennis, James W.
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container_issue
container_start_page 53
container_title Analytica chimica acta
container_volume 845
creator Abdel Rahman, Anas M.
Pawling, Judy
Ryczko, Michael
Caudy, Amy A.
Dennis, James W.
description [Display omitted] •This study introduce a valid bioanalytical method for metabolic profiling.•The method validation and stability were studied carefully based on USFDA guidelines.•The targeted metabolomics method was tested on couple of biological systems cell lines and mouse tissue. Metabolomics is the identification and quantitation of small bio-molecules (metabolites) in biological samples under various environmental and genetic conditions. Mass spectrometry provides the unique opportunity for targeted identification and quantification of known metabolites by selective reaction monitoring (SRM). However, reproducibility of this approach depends on careful consideration of sample preparation, chemical classes, and stability of metabolites to be evaluated. Herein, we introduce and validate a targeted metabolite profiling workflow for cultured cells and tissues by liquid chromatography–triple quadrupole tandem mass spectrometry. The method requires a one-step extraction of water-soluble metabolites and targeted analysis of central metabolites that include glycolysis, amino acids, nucleotides, citric acid cycle, and the hexosamine biosynthetic pathway. The sensitivity, reproducibility and molecular stability of each targeted metabolite were assessed under experimental conditions. Quantitation of metabolites by peak area ratio was linear with a dilution over a 4 fold dynamic range with minimal deviation R2=0.98. Inter- and intra-day precision with cells and tissues had an average coefficient of variation
doi_str_mv 10.1016/j.aca.2014.06.012
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subjects Amino acids
Amino Acids - analysis
Amino Acids - metabolism
Animals
Biological
Cells, Cultured
Citric Acid - analysis
Citric Acid - metabolism
Citric Acid Cycle
Deviation
Diagnostics
Extraction
HEK293 Cells
HeLa Cells
Hexosamines - analysis
Hexosamines - biosynthesis
Humans
Mass Spectrometry
Metabolism
Metabolites
Metabolomics - methods
Mice
Nucleotides - analysis
Nucleotides - metabolism
Precision
Reproducibility
Sensitivity
Stability
title Targeted metabolomics in cultured cells and tissues by mass spectrometry: Method development and validation
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