Abstract
With the growing interest in the use of breath volatiles in the health sciences, the lack of standardization for the sampling and analysis of exhaled breath is becoming a major issue leading to an absence of conformity, reproducibility and reliability in spectrometric measurements. Through the creation of a worldwide ‘peppermint consortium’, the International Association of Breath Research has set up a task force to deal with this problem. Pharmacokinetic studies are proposed, and a real-time analytical technique that is being used is proton transfer reaction-time-of-flight-mass spectrometry (PTR-ToF-MS). This paper presents details on how the volatile compounds contained in a peppermint oil capsule, and hence on breath, appear in a PTR-ToF-MS. To aid that study, the key volatiles in the headspace of peppermint oil were first identified using gas chromatography-mass spectrometry, notably: menthol, menthone, 1,8-cineole, menthofuran, limonene, α-pinene and β-pinene. A PTR-ToF-MS analysis of these compounds has been undertaken, divorced from the complexity of the peppermint oil matrix using ‘normal’ and ‘saturated’ humidity drift-tube conditions, with the latter used to mimic breath samples, and over a range of reduced electric fields. There are no characteristic product ions that can distinguish monoterpenes and 1,8-cineole, and hence, without pre-separation, a combined washout for these volatiles can only be provided. By operating the drift tube above about 130 Td, there are characteristic product ions for menthone, menthofuran and menthol, namely m/z 155.14 (protonated menthone), m/z 151.11 (protonated menthofuran), m/z 139.15 (loss of H2O from protonated menthol) and m/z 83.09 (a fragment ion, C6H11+, from menthol). These have been used to monitor, with a high specificity, the temporal profile of these three compounds in breath following the ingestion of a peppermint oil capsule. To aid in the analyses, the proton affinities and gas-phase basicities for the key volatiles investigated have been determined using density functional theory.
Highlights
Real-time analysis of exogenous volatiles contained in breath is suited for pharmacokinetic studies
We present details of PTR-ToF-MS investigations on the key individual volatile compounds that have been identified by gas chromatography-mass spectrometry (GC-MS) to be contained in the specific peppermint oil capsules being used by the consortium
GC-MS determination of the volatiles present in peppermint oil A large number of volatile compounds were identified from the GC-MS analysis of the headspace of the peppermint oil contained in the specific capsules (Boots Pharmaceuticals, UK) that are being used by the peppermint consortium
Summary
Real-time analysis of exogenous volatiles contained in breath is suited for pharmacokinetic studies. [10,11,12] These techniques are ideal for breath-to-breath analysis and pharmacokinetic breath studies [13]. There are no agreed sampling and analysis protocols for real-time (and off-line) breath studies. This results from the large variety of volatiles present in breath, the many different diseases being investigated, the diversity of breath sampling and collection methods and the diverse array of analytical instruments. Standardization is a high priority issue for the breath research community if independent studies are to be compared and in order to establish reliable and reproducible approaches and results if breath tests are to be of any use in a clinical environment [14, 15]
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