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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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 |
format | Article |
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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><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2017.12.025</identifier><identifier>PMID: 30016264</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>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</subject><ispartof>Analytica chimica acta, 2018-05, Vol.1006, p.49-60</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV May 2, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-211978887aa4c379ce830a53c6f8f400e134a3ead14d45774fac78263d0daed63</citedby><cites>FETCH-LOGICAL-c479t-211978887aa4c379ce830a53c6f8f400e134a3ead14d45774fac78263d0daed63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0003267017314484$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30016264$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zamuruyev, Konstantin O.</creatorcontrib><creatorcontrib>Borras, Eva</creatorcontrib><creatorcontrib>Pettit, Dayna R.</creatorcontrib><creatorcontrib>Aksenov, Alexander A.</creatorcontrib><creatorcontrib>Simmons, Jason D.</creatorcontrib><creatorcontrib>Weimer, Bart C.</creatorcontrib><creatorcontrib>Schivo, Michael</creatorcontrib><creatorcontrib>Kenyon, Nicholas J.</creatorcontrib><creatorcontrib>Delplanque, Jean-Pierre</creatorcontrib><creatorcontrib>Davis, Cristina E.</creatorcontrib><title>Effect of temperature control on the metabolite content in exhaled breath condensate</title><title>Analytica chimica acta</title><addtitle>Anal Chim Acta</addtitle><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 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. ; 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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-211978887aa4c379ce830a53c6f8f400e134a3ead14d45774fac78263d0daed63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adhesion</topic><topic>Analytical methods</topic><topic>Breath metabolomics</topic><topic>Breath Tests - instrumentation</topic><topic>Breath Tests - methods</topic><topic>Chemical reactions</topic><topic>Collection</topic><topic>Collection temperature control</topic><topic>Condensates</topic><topic>Condensation</topic><topic>Design parameters</topic><topic>Diagnostic systems</topic><topic>Dilution</topic><topic>Equipment Design</topic><topic>Exhalation</topic><topic>Exhaled breath condensate (EBC)</topic><topic>Filtration</topic><topic>Humans</topic><topic>Mass spectrometry</topic><topic>Mass Spectrometry - instrumentation</topic><topic>Mass spectroscopy</topic><topic>Metabolites</topic><topic>Metabolomics</topic><topic>Metabolomics - instrumentation</topic><topic>Metabolomics - methods</topic><topic>Polarity</topic><topic>Saliva</topic><topic>Sampling methods</topic><topic>Standardization</topic><topic>Temperature</topic><topic>Temperature control</topic><topic>Temperature dependence</topic><topic>Temperature effects</topic><topic>Temperature requirements</topic><topic>Volatile compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zamuruyev, Konstantin O.</creatorcontrib><creatorcontrib>Borras, Eva</creatorcontrib><creatorcontrib>Pettit, Dayna R.</creatorcontrib><creatorcontrib>Aksenov, Alexander A.</creatorcontrib><creatorcontrib>Simmons, Jason D.</creatorcontrib><creatorcontrib>Weimer, Bart C.</creatorcontrib><creatorcontrib>Schivo, Michael</creatorcontrib><creatorcontrib>Kenyon, Nicholas J.</creatorcontrib><creatorcontrib>Delplanque, Jean-Pierre</creatorcontrib><creatorcontrib>Davis, Cristina E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Analytica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zamuruyev, Konstantin O.</au><au>Borras, Eva</au><au>Pettit, Dayna R.</au><au>Aksenov, Alexander A.</au><au>Simmons, Jason D.</au><au>Weimer, Bart C.</au><au>Schivo, Michael</au><au>Kenyon, Nicholas J.</au><au>Delplanque, Jean-Pierre</au><au>Davis, Cristina E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of temperature control on the metabolite content in exhaled breath condensate</atitle><jtitle>Analytica chimica acta</jtitle><addtitle>Anal Chim Acta</addtitle><date>2018-05-02</date><risdate>2018</risdate><volume>1006</volume><spage>49</spage><epage>60</epage><pages>49-60</pages><issn>0003-2670</issn><eissn>1873-4324</eissn><abstract>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 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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