Sampling and Analysis of Low-Molecular-Weight Volatile Metabolites in Cellular Headspace and Mouse Breath.
Theo IssittSean T SweeneyWilliam John BrackenburyKelly R RedekerPublished in: Metabolites (2022)
Volatile compounds, abundant in breath, can be used to accurately diagnose and monitor a range of medical conditions. This offers a noninvasive, low-cost approach with screening applications; however, the uptake of this diagnostic approach has been limited by conflicting published outcomes. Most published reports rely on large scale screening of the public, at single time points and without reference to ambient air. Here, we present a novel approach to volatile sampling from cellular headspace and mouse breath that incorporates multi-time-point analysis and ambient air subtraction revealing compound flux as an effective proxy of active metabolism. This approach to investigating breath volatiles offers a new avenue for disease biomarker discovery and diagnosis. Using gas chromatography mass spectrometry (GC/MS), we focus on low molecular weight, metabolic substrate/by-product compounds and demonstrate that this noninvasive technique is sensitive (reproducible at ~1 µg cellular protein, or ~500,000 cells) and capable of precisely determining cell type, status and treatment. Isolated cellular models represent components of larger mammalian systems, and we show that stress- and pathology-indicative compounds are detectable in mice, supporting further investigation using this methodology as a tool to identify volatile targets in human patients.
Keyphrases
- gas chromatography mass spectrometry
- gas chromatography
- mass spectrometry
- tandem mass spectrometry
- low cost
- air pollution
- solid phase extraction
- particulate matter
- healthcare
- end stage renal disease
- newly diagnosed
- endothelial cells
- ejection fraction
- peritoneal dialysis
- small molecule
- prognostic factors
- ms ms
- systematic review
- mental health
- adverse drug
- cell proliferation
- high throughput
- cell cycle arrest
- oxidative stress
- patient reported
- computed tomography
- simultaneous determination
- cell death
- stress induced
- single cell
- pluripotent stem cells