Abstract

Exposure to oxygen under increased atmospheric pressures can induce pulmonary oxygen toxicity (POT). Exhaled breath analysis using gas chromatography–mass spectrometry (GC–MS) has revealed that volatile organic compounds (VOCs) are associated with inflammation and lipoperoxidation after hyperbaric–hyperoxic exposure. Electronic nose (eNose) technology would be more suited for the detection of POT, since it is less time and resource consuming. However, it is unknown whether eNose technology can detect POT and whether eNose sensor data can be associated with VOCs of interest. In this randomized cross-over trial, the exhaled breath from divers who had made two dives of 1 h to 192.5 kPa (a depth of 9 m) with either 100% oxygen or compressed air was analyzed, at several time points, using GC–MS and eNose. We used a partial least square discriminant analysis, eNose discriminated oxygen and air dives at 30 min post dive with an area under the receiver operating characteristics curve of 79.9% (95%CI: 61.1–98.6; p = 0.003). A two-way orthogonal partial least square regression (O2PLS) model analysis revealed an R² of 0.50 between targeted VOCs obtained by GC–MS and eNose sensor data. The contribution of each sensor to the detection of targeted VOCs was also assessed using O2PLS. When all GC–MS fragments were included in the O2PLS model, this resulted in an R² of 0.08. Thus, eNose could detect POT 30 min post dive, and the correlation between targeted VOCs and eNose data could be assessed using O2PLS.

Highlights

  • Prolonged exposition to hyperoxia can induce pulmonary oxygen toxicity (POT) [1,2]

  • The Electronic nose (eNose) optimally differentiated oxygen and air dives at 30 min post dive with an area under curve (AUC) of 79.9% and a p-value of 0.003 (Figure 1b)

  • This study shows that POT can be detected 30 min post dive using eNose, while at other time points post dive detection is poor and not statistically significant

Read more

Summary

Introduction

Prolonged exposition to hyperoxia can induce pulmonary oxygen toxicity (POT) [1,2]. In diving and hyperbaric medicine, where oxygen is breathed under increased atmospheric pressures, the risk of developing POT is severe [3]. To prevent POT from occurring, oxygen exposure under increased atmospheric pressure is maintained within strict limits [4,5]. Metabolites 2019, 9, 286 these limits are based on dated research and are inaccurate, no valid alternative to prevent POT has been developed [3,6,7]. Recent studies, using exhaled breath analysis by gas chromatography-mass spectrometry (GC–MS), have revealed markers of POT-associated inflammation (such as cyclohexane) and lipoperoxidation of alveolar membranes (several methyl alkanes) as compounds of interest [8,9,10]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call