Breath gas analysis

Breath gas analysis

From Wikipedia, the free encyclopedia

Breath gas analysis is a method for gaining non-invasive information on the clinical state of an individual by monitoring volatile organic compoundspresent in the exhaled breath. Breath gas concentration can then be related to blood concentrations via mathematical modeling as for example inblood alcohol testing.


The area of modern breath testing commenced in 1971, when Nobel Prize winner Linus Pauling demonstrated that human breath is a complex gas, containing more than 200 different volatile organic compounds. However, physicians have used breath analysis since the days of Hippocrates.[1]


Endogenous volatile organic compounds (VOCs) are released within the human organism as a result of normal metabolic activity or due to pathological disorders. They enter the blood stream and are eventually metabolized or excreted via exhalationskin emission, urine, etc.

Breath sampling is non-invasive and breath samples can be extracted as often as desired.[2]

Identification and quantification of potential disease biomarkers can be seen as the driving force for the analysis of exhaled breath. Moreover, future applications for medical diagnosis and therapy control with dynamic assessments of normal physiological function or pharmacodynamics are intended.

Exogenous VOCs penetrating the body as a result of environmental exposure can be used to quantify body burden. Also breath tests are often based on the ingestion of isotopically labeled precursors, producing isotopically labeled carbon dioxide and potentially many other metabolites.

However, breath sampling is far from being a standardized procedure due to the numerous confounding factors biasing the concentrations of volatiles in breath. These factors are related to both the breath sampling protocols as well as the complex physiological mechanisms underlying pulmonary gas exchange. Even under resting conditions exhaled breath concentrations of VOCs can strongly be influenced by specific physiological parameters such as cardiac output and breathing patterns, depending on the physico-chemical properties of the compound under study.

Understanding the influence of all this factors and their control is necessary for achieving an accurate standardization of breath sample collection and for the correct deduction of the corresponding blood concentration levels.

The simplest model relating breath gas concentration to blood concentrations was developed by Farhi[3]

C_A = \frac{C_{\bar v}}{\lambda_\text{b:air} + \dot V_A/\dot Q_c},

where  C_A  denotes the alveolar concentration which is assumed to be equal to the measured concentration. It expresses the fact that the concentration of an inert gas in the alveolar air depends on the mixed venous concentration C_{\bar v} , the substance-specific blood:air partition coefficient \lambda_\text{b:air} , and the ventilation-perfusion ratio \dot V_A/\dot Q_c . But this model fails when two prototypical substances like acetone (partition coefficient \lambda_\text{b:air} = 340 ) or isoprene (partition coefficient \lambda_\text{b:air} = 0.75   ) are measured.[4]

E.g., multiplying the proposed population mean of approximately  1 \mu g/l  acetone in end-tidal breath by the partition coefficient \lambda_\text{b:air} = 340  at body temperature grossly underestimates observed (arterial) blood levels spreading around  1 mg/l . Furthermore, breath profiles of acetone (and other highly soluble volatile compounds such as 2-pentanone or methyl acetate) associated with moderate workload ergometer challenges of normal healthy volunteers drastically depart from the trend suggested by the equation above.

Hence some more refined models are necessary. Such models have been developed recently.[5][6]


Breath gas analysis is used in a number of breath tests.

Analytical instruments[edit]

Breath analysis can be done with various forms of mass spectrometry, but there are also simpler methods for specific purposes, such as theHalimeter and the breathalyzer.


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