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Automated Solid Phase Extraction and Polarity-Switching Tandem Mass Spectrometry Technique for High Throughput Analysis of Urine Biomarkers for 14 Tobacco-related Compounds
[Image: see text] Tobacco use is the leading preventable cause of premature disease and death in the United States. Approximately, 34 million U.S. adults currently smoke cigarettes. We developed a method for automated sample preparation and liquid chromatography-tandem mass spectrometry quantitation...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613820/ https://www.ncbi.nlm.nih.gov/pubmed/34841133 http://dx.doi.org/10.1021/acsomega.1c02543 |
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author | Piyankarage, Sujeewa C. McGahee, Ernest Feng, June Blount, Benjamin C. Wang, Lanqing |
author_facet | Piyankarage, Sujeewa C. McGahee, Ernest Feng, June Blount, Benjamin C. Wang, Lanqing |
author_sort | Piyankarage, Sujeewa C. |
collection | PubMed |
description | [Image: see text] Tobacco use is the leading preventable cause of premature disease and death in the United States. Approximately, 34 million U.S. adults currently smoke cigarettes. We developed a method for automated sample preparation and liquid chromatography-tandem mass spectrometry quantitation of 14 tobacco-related analytes: nicotine (NICF), cotinine (COTF), trans-3′-hydroxycotinine (HCTF), menthol glucuronide (MEG), anabasine (ANBF), anatabine (ANTF), isonicoteine (ISNT), myosmine (MYOS), beta-nicotyrine (BNTR), bupropion (BUPR), cytisine (CYTI), varenicline (VARE), arecaidine (ARD), and arecoline (ARL). The method includes automated solid-phase extraction using customized positive-pressure functions. The preparation scheme has the capacity to process a batch of 96 samples within 4 h with greater than 88% recovery for all analytes. The 14 analytes, separated within 4.15 min using reversed-phase liquid chromatography, were determined using a triple-quadrupole mass spectrometer with atmospheric-pressure chemical ionization and multiple reaction monitoring in negative and positive ionization modes. Wide quantitation ranges, within 1.2–72,000 ng/mL, were established especially for COTF, HCTF, MEG, and NICF to quantify the broad range of biomarker concentrations found in the U.S. population. The method accuracy is above 90% while the overall imprecision is below 7%. Finally, we tested urine samples from 90 smokers and observed detection rates of over 98% for six analytes with urinary HCTF and MEG concentrations ranging from 200–14,100 and 60–57,100 ng/mL, respectively. This high throughput analytical process can prepare and analyze a sample in 9 min and along with the 14-compound analyte panel can be useful for tobacco-exposure studies, in smoking-cessation programs, and for detecting changes in exposure related to tobacco products and their use. |
format | Online Article Text |
id | pubmed-8613820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-86138202021-11-26 Automated Solid Phase Extraction and Polarity-Switching Tandem Mass Spectrometry Technique for High Throughput Analysis of Urine Biomarkers for 14 Tobacco-related Compounds Piyankarage, Sujeewa C. McGahee, Ernest Feng, June Blount, Benjamin C. Wang, Lanqing ACS Omega [Image: see text] Tobacco use is the leading preventable cause of premature disease and death in the United States. Approximately, 34 million U.S. adults currently smoke cigarettes. We developed a method for automated sample preparation and liquid chromatography-tandem mass spectrometry quantitation of 14 tobacco-related analytes: nicotine (NICF), cotinine (COTF), trans-3′-hydroxycotinine (HCTF), menthol glucuronide (MEG), anabasine (ANBF), anatabine (ANTF), isonicoteine (ISNT), myosmine (MYOS), beta-nicotyrine (BNTR), bupropion (BUPR), cytisine (CYTI), varenicline (VARE), arecaidine (ARD), and arecoline (ARL). The method includes automated solid-phase extraction using customized positive-pressure functions. The preparation scheme has the capacity to process a batch of 96 samples within 4 h with greater than 88% recovery for all analytes. The 14 analytes, separated within 4.15 min using reversed-phase liquid chromatography, were determined using a triple-quadrupole mass spectrometer with atmospheric-pressure chemical ionization and multiple reaction monitoring in negative and positive ionization modes. Wide quantitation ranges, within 1.2–72,000 ng/mL, were established especially for COTF, HCTF, MEG, and NICF to quantify the broad range of biomarker concentrations found in the U.S. population. The method accuracy is above 90% while the overall imprecision is below 7%. Finally, we tested urine samples from 90 smokers and observed detection rates of over 98% for six analytes with urinary HCTF and MEG concentrations ranging from 200–14,100 and 60–57,100 ng/mL, respectively. This high throughput analytical process can prepare and analyze a sample in 9 min and along with the 14-compound analyte panel can be useful for tobacco-exposure studies, in smoking-cessation programs, and for detecting changes in exposure related to tobacco products and their use. American Chemical Society 2021-11-12 /pmc/articles/PMC8613820/ /pubmed/34841133 http://dx.doi.org/10.1021/acsomega.1c02543 Text en Not subject to U.S. Copyright. Published 2021 by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Piyankarage, Sujeewa C. McGahee, Ernest Feng, June Blount, Benjamin C. Wang, Lanqing Automated Solid Phase Extraction and Polarity-Switching Tandem Mass Spectrometry Technique for High Throughput Analysis of Urine Biomarkers for 14 Tobacco-related Compounds |
title | Automated Solid Phase Extraction and Polarity-Switching
Tandem Mass Spectrometry Technique for High Throughput Analysis of
Urine Biomarkers for 14 Tobacco-related Compounds |
title_full | Automated Solid Phase Extraction and Polarity-Switching
Tandem Mass Spectrometry Technique for High Throughput Analysis of
Urine Biomarkers for 14 Tobacco-related Compounds |
title_fullStr | Automated Solid Phase Extraction and Polarity-Switching
Tandem Mass Spectrometry Technique for High Throughput Analysis of
Urine Biomarkers for 14 Tobacco-related Compounds |
title_full_unstemmed | Automated Solid Phase Extraction and Polarity-Switching
Tandem Mass Spectrometry Technique for High Throughput Analysis of
Urine Biomarkers for 14 Tobacco-related Compounds |
title_short | Automated Solid Phase Extraction and Polarity-Switching
Tandem Mass Spectrometry Technique for High Throughput Analysis of
Urine Biomarkers for 14 Tobacco-related Compounds |
title_sort | automated solid phase extraction and polarity-switching
tandem mass spectrometry technique for high throughput analysis of
urine biomarkers for 14 tobacco-related compounds |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613820/ https://www.ncbi.nlm.nih.gov/pubmed/34841133 http://dx.doi.org/10.1021/acsomega.1c02543 |
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