Aim: Breath analyses have potential to detect early signs of disease onset. Ambient ionization allows direct combination of breath gases with MS for fast, on-line analysis. Portable MS systems would facilitate field/clinic-based breath analyses.
View Article and Find Full Text PDFThermal desorption is used extensively in exhaled breath volatile organic compound (VOC) analysis, and it is often necessary to store the adsorbent tube samples before analysis. The possible introduction of storage artefacts is an important potential confounding factor in the development of standard methodologies for breath sampling and analysis. The stability of VOCs trapped from breath samples onto a dual bed Tenax(®) TA:Carbograph adsorbent tube and stored -80°C was studied over 12.
View Article and Find Full Text PDFA two-stage thermal desorption/secondary electrospray ionization/time-of-flight mass spectrometry for faster targeted breath profiling has been studied. A new secondary electrospray ionization (SESI) source was devised to constrain the thermal desorption plume and promote efficient mixing in the ionization region. Further, a chromatographic pre-separation stage was introduced to suppress interferences from siloxanes associated with thermal desorption profiles of exhaled breath samples.
View Article and Find Full Text PDFBackground: In-community non-invasive identification of asthma-specific volatile organic compounds (VOCs) in exhaled breath presents opportunities to characterize phenotypes, and monitor disease state and therapies. The feasibility of breath sampling with children and the preliminary identification of childhood asthma markers were studied.
Method: End-tidal exhaled breath was sampled (2.
A gas-phase on-fibre derivatisation method for the determination of putrescine and cadaverine by gas chromatography/mass spectrometry using trifluoroacetylacetone (TFAA) has been studied and optimised. Small amounts (2μl) of putrescine, cadaverine and TFAA standards were vaporised at high temperature in a 20cm(3) closed SPME vial. The subsequent derivatives were recovered from the headspace of the vial using a PDMS/DVB fibre.
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