Effect of temperature control on the metabolite content in exhaled breath condensate

The non-invasive, quick, and safe collection of exhaled breath condensate makes it a candidate as a diagnostic matrix in personalized health monitoring devices. The lack of standardization in collection methods and sample analysis is a persistent limitation preventing its practical use. The collecti...

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Veröffentlicht in:Analytica chimica acta 2018-05, Vol.1006, p.49-60
Hauptverfasser: Zamuruyev, Konstantin O., Borras, Eva, Pettit, Dayna R., Aksenov, Alexander A., Simmons, Jason D., Weimer, Bart C., Schivo, Michael, Kenyon, Nicholas J., Delplanque, Jean-Pierre, Davis, Cristina E.
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container_issue
container_start_page 49
container_title Analytica chimica acta
container_volume 1006
creator Zamuruyev, Konstantin O.
Borras, Eva
Pettit, Dayna R.
Aksenov, Alexander A.
Simmons, Jason D.
Weimer, Bart C.
Schivo, Michael
Kenyon, Nicholas J.
Delplanque, Jean-Pierre
Davis, Cristina E.
description The non-invasive, quick, and safe collection of exhaled breath condensate makes it a candidate as a diagnostic matrix in personalized health monitoring devices. The lack of standardization in collection methods and sample analysis is a persistent limitation preventing its practical use. The collection method and hardware design are recognized to significantly affect the metabolomic content of EBC samples, but this has not been systematically studied. Here, we completed a series of experiments to determine the sole effect of collection temperature on the metabolomic content of EBC. Temperature is a likely parameter that can be controlled to standardize among different devices. The study considered six temperature levels covering two physical phases of the sample; liquid and solid. The use of a single device in our study allowed keeping saliva filtering and collector surface effects as constant parameters and the temperature as a controlled variable; the physiological differences were minimized by averaging samples from a group of volunteers and a period of time. After EBC collection, we used an organic solvent rinse to collect the non-water-soluble compounds from the condenser surface. This additional matrix enhanced metabolites recovery, was less dependent on temperature changes, and may possibly serve as an additional pointer to standardize EBC sampling methodologies. The collected EBC samples were analyzed with a set of mass spectrometry methods to provide an overview of the compounds and their concentrations present at each temperature level. The total number of volatile and polar non-volatile compounds slightly increased in each physical phase as the collection temperature was lowered to minimum, 0 °C for liquid and −30, −56 °C for solid. The low-polarity non-volatile compounds showed a weak dependence on the collection temperature. The metabolomic content of EBC samples may not be solely dependent on temperature but may be influenced by other phenomena such as greater sample dilution due to condensation from the ambient air at colder temperatures, or due to adhesion properties of the collector surface and occurring chemical reactions. The relative importance of other design parameters such as condenser coating versus temperature requires further investigation. [Display omitted] •Effect of temperature control and sample physical phase on the metabolomic content of exhaled breath condensate.•Concentration of volatile compounds detected with GC-MS and no
doi_str_mv 10.1016/j.aca.2017.12.025
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After EBC collection, we used an organic solvent rinse to collect the non-water-soluble compounds from the condenser surface. This additional matrix enhanced metabolites recovery, was less dependent on temperature changes, and may possibly serve as an additional pointer to standardize EBC sampling methodologies. The collected EBC samples were analyzed with a set of mass spectrometry methods to provide an overview of the compounds and their concentrations present at each temperature level. The total number of volatile and polar non-volatile compounds slightly increased in each physical phase as the collection temperature was lowered to minimum, 0 °C for liquid and −30, −56 °C for solid. The low-polarity non-volatile compounds showed a weak dependence on the collection temperature. The metabolomic content of EBC samples may not be solely dependent on temperature but may be influenced by other phenomena such as greater sample dilution due to condensation from the ambient air at colder temperatures, or due to adhesion properties of the collector surface and occurring chemical reactions. The relative importance of other design parameters such as condenser coating versus temperature requires further investigation. 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The lack of standardization in collection methods and sample analysis is a persistent limitation preventing its practical use. The collection method and hardware design are recognized to significantly affect the metabolomic content of EBC samples, but this has not been systematically studied. Here, we completed a series of experiments to determine the sole effect of collection temperature on the metabolomic content of EBC. Temperature is a likely parameter that can be controlled to standardize among different devices. The study considered six temperature levels covering two physical phases of the sample; liquid and solid. The use of a single device in our study allowed keeping saliva filtering and collector surface effects as constant parameters and the temperature as a controlled variable; the physiological differences were minimized by averaging samples from a group of volunteers and a period of time. After EBC collection, we used an organic solvent rinse to collect the non-water-soluble compounds from the condenser surface. This additional matrix enhanced metabolites recovery, was less dependent on temperature changes, and may possibly serve as an additional pointer to standardize EBC sampling methodologies. The collected EBC samples were analyzed with a set of mass spectrometry methods to provide an overview of the compounds and their concentrations present at each temperature level. The total number of volatile and polar non-volatile compounds slightly increased in each physical phase as the collection temperature was lowered to minimum, 0 °C for liquid and −30, −56 °C for solid. The low-polarity non-volatile compounds showed a weak dependence on the collection temperature. The metabolomic content of EBC samples may not be solely dependent on temperature but may be influenced by other phenomena such as greater sample dilution due to condensation from the ambient air at colder temperatures, or due to adhesion properties of the collector surface and occurring chemical reactions. The relative importance of other design parameters such as condenser coating versus temperature requires further investigation. [Display omitted] •Effect of temperature control and sample physical phase on the metabolomic content of exhaled breath condensate.•Concentration of volatile compounds detected with GC-MS and non-volatiles detected with HILIC LC-MS are temperature influenced.•Detection of specific types of compounds may be more efficient at a specific temperature.•The importance of temperature control relative to saliva filtering and surface coatings needs to be further investigated.</description><subject>Adhesion</subject><subject>Analytical methods</subject><subject>Breath metabolomics</subject><subject>Breath Tests - instrumentation</subject><subject>Breath Tests - methods</subject><subject>Chemical reactions</subject><subject>Collection</subject><subject>Collection temperature control</subject><subject>Condensates</subject><subject>Condensation</subject><subject>Design parameters</subject><subject>Diagnostic systems</subject><subject>Dilution</subject><subject>Equipment Design</subject><subject>Exhalation</subject><subject>Exhaled breath condensate (EBC)</subject><subject>Filtration</subject><subject>Humans</subject><subject>Mass spectrometry</subject><subject>Mass Spectrometry - instrumentation</subject><subject>Mass spectroscopy</subject><subject>Metabolites</subject><subject>Metabolomics</subject><subject>Metabolomics - instrumentation</subject><subject>Metabolomics - methods</subject><subject>Polarity</subject><subject>Saliva</subject><subject>Sampling methods</subject><subject>Standardization</subject><subject>Temperature</subject><subject>Temperature control</subject><subject>Temperature dependence</subject><subject>Temperature effects</subject><subject>Temperature requirements</subject><subject>Volatile compounds</subject><issn>0003-2670</issn><issn>1873-4324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU-LFDEQxYMo7rj6AbxIgxcv3Vb-dKcbQViWdRUWvKznUJNUOxm6O2OSXtZvb4ZZF_XgKYT3e4-qeoy95tBw4N37fYMWGwFcN1w0INonbMN7LWslhXrKNgAga9FpOGMvUtqXr-CgnrMzCcUuOrVht1fjSDZXYawyzQeKmNdIlQ1LjmGqwlLlHVUzZdyGyeeTQkuu_FLR_Q4nctU2EubdUXG0JMz0kj0bcUr06uE9Z98-Xd1efq5vvl5_uby4qa3SQ64F54Pu-14jKiv1YKmXgK203diPCoC4VCgJHVdOtVqrEa3uRScdOCTXyXP28ZR7WLczOVvmijiZQ_Qzxp8moDd_K4vfme_hznTQwtDLEvDuISCGHyulbGafLE0TLhTWZARo3molBl3Qt_-g-7DGpaxXKD6A6KEdCsVPlI0hpUjj4zAczLEzszels6NFGy5M6ax43vy5xaPjd0kF-HACqNzyzlM0yXpaLDkfS3fGBf-f-F-zuaeJ</recordid><startdate>20180502</startdate><enddate>20180502</enddate><creator>Zamuruyev, Konstantin O.</creator><creator>Borras, Eva</creator><creator>Pettit, Dayna R.</creator><creator>Aksenov, Alexander A.</creator><creator>Simmons, Jason D.</creator><creator>Weimer, Bart C.</creator><creator>Schivo, Michael</creator><creator>Kenyon, Nicholas J.</creator><creator>Delplanque, Jean-Pierre</creator><creator>Davis, Cristina E.</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180502</creationdate><title>Effect of temperature control on the metabolite content in exhaled breath condensate</title><author>Zamuruyev, Konstantin O. ; 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The lack of standardization in collection methods and sample analysis is a persistent limitation preventing its practical use. The collection method and hardware design are recognized to significantly affect the metabolomic content of EBC samples, but this has not been systematically studied. Here, we completed a series of experiments to determine the sole effect of collection temperature on the metabolomic content of EBC. Temperature is a likely parameter that can be controlled to standardize among different devices. The study considered six temperature levels covering two physical phases of the sample; liquid and solid. The use of a single device in our study allowed keeping saliva filtering and collector surface effects as constant parameters and the temperature as a controlled variable; the physiological differences were minimized by averaging samples from a group of volunteers and a period of time. After EBC collection, we used an organic solvent rinse to collect the non-water-soluble compounds from the condenser surface. This additional matrix enhanced metabolites recovery, was less dependent on temperature changes, and may possibly serve as an additional pointer to standardize EBC sampling methodologies. The collected EBC samples were analyzed with a set of mass spectrometry methods to provide an overview of the compounds and their concentrations present at each temperature level. The total number of volatile and polar non-volatile compounds slightly increased in each physical phase as the collection temperature was lowered to minimum, 0 °C for liquid and −30, −56 °C for solid. The low-polarity non-volatile compounds showed a weak dependence on the collection temperature. The metabolomic content of EBC samples may not be solely dependent on temperature but may be influenced by other phenomena such as greater sample dilution due to condensation from the ambient air at colder temperatures, or due to adhesion properties of the collector surface and occurring chemical reactions. The relative importance of other design parameters such as condenser coating versus temperature requires further investigation. [Display omitted] •Effect of temperature control and sample physical phase on the metabolomic content of exhaled breath condensate.•Concentration of volatile compounds detected with GC-MS and non-volatiles detected with HILIC LC-MS are temperature influenced.•Detection of specific types of compounds may be more efficient at a specific temperature.•The importance of temperature control relative to saliva filtering and surface coatings needs to be further investigated.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30016264</pmid><doi>10.1016/j.aca.2017.12.025</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Adhesion
Analytical methods
Breath metabolomics
Breath Tests - instrumentation
Breath Tests - methods
Chemical reactions
Collection
Collection temperature control
Condensates
Condensation
Design parameters
Diagnostic systems
Dilution
Equipment Design
Exhalation
Exhaled breath condensate (EBC)
Filtration
Humans
Mass spectrometry
Mass Spectrometry - instrumentation
Mass spectroscopy
Metabolites
Metabolomics
Metabolomics - instrumentation
Metabolomics - methods
Polarity
Saliva
Sampling methods
Standardization
Temperature
Temperature control
Temperature dependence
Temperature effects
Temperature requirements
Volatile compounds
title Effect of temperature control on the metabolite content in exhaled breath condensate
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