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E-Cigarette Flavoring Chemicals Induce Cytotoxicity in HepG2 Cells
[Image: see text] E-cigarette-related hospitalizations and deaths across the U.S. continue to increase. A high percentage of patients have elevated liver function tests indicative of systemic toxicity. This study was designed to determine the effect of e-cigarette chemicals on liver cell toxicity. H...
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/PMC7970492/ https://www.ncbi.nlm.nih.gov/pubmed/33748584 http://dx.doi.org/10.1021/acsomega.0c05639 |
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author | Rickard, Brittany P. Ho, Henry Tiley, Jacqueline B. Jaspers, Ilona Brouwer, Kim L. R. |
author_facet | Rickard, Brittany P. Ho, Henry Tiley, Jacqueline B. Jaspers, Ilona Brouwer, Kim L. R. |
author_sort | Rickard, Brittany P. |
collection | PubMed |
description | [Image: see text] E-cigarette-related hospitalizations and deaths across the U.S. continue to increase. A high percentage of patients have elevated liver function tests indicative of systemic toxicity. This study was designed to determine the effect of e-cigarette chemicals on liver cell toxicity. HepG2 cells were exposed to flavoring chemicals (isoamyl acetate, vanillin, ethyl vanillin, ethyl maltol, l-menthol, and trans-cinnamaldehyde), propylene glycol, and vegetable glycerin mixtures, and cell viability was measured. Data revealed that vanillin, ethyl vanillin, and ethyl maltol decreased HepG2 cell viability; repeated exposure caused increased cytotoxicity relative to single exposure, consistent with the hypothesis that frequent vaping can cause hepatotoxicity. |
format | Online Article Text |
id | pubmed-7970492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79704922021-03-19 E-Cigarette Flavoring Chemicals Induce Cytotoxicity in HepG2 Cells Rickard, Brittany P. Ho, Henry Tiley, Jacqueline B. Jaspers, Ilona Brouwer, Kim L. R. ACS Omega [Image: see text] E-cigarette-related hospitalizations and deaths across the U.S. continue to increase. A high percentage of patients have elevated liver function tests indicative of systemic toxicity. This study was designed to determine the effect of e-cigarette chemicals on liver cell toxicity. HepG2 cells were exposed to flavoring chemicals (isoamyl acetate, vanillin, ethyl vanillin, ethyl maltol, l-menthol, and trans-cinnamaldehyde), propylene glycol, and vegetable glycerin mixtures, and cell viability was measured. Data revealed that vanillin, ethyl vanillin, and ethyl maltol decreased HepG2 cell viability; repeated exposure caused increased cytotoxicity relative to single exposure, consistent with the hypothesis that frequent vaping can cause hepatotoxicity. American Chemical Society 2021-03-02 /pmc/articles/PMC7970492/ /pubmed/33748584 http://dx.doi.org/10.1021/acsomega.0c05639 Text en © 2021 The Authors. Published by American Chemical Society 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 | Rickard, Brittany P. Ho, Henry Tiley, Jacqueline B. Jaspers, Ilona Brouwer, Kim L. R. E-Cigarette Flavoring Chemicals Induce Cytotoxicity in HepG2 Cells |
title | E-Cigarette Flavoring Chemicals Induce Cytotoxicity
in HepG2 Cells |
title_full | E-Cigarette Flavoring Chemicals Induce Cytotoxicity
in HepG2 Cells |
title_fullStr | E-Cigarette Flavoring Chemicals Induce Cytotoxicity
in HepG2 Cells |
title_full_unstemmed | E-Cigarette Flavoring Chemicals Induce Cytotoxicity
in HepG2 Cells |
title_short | E-Cigarette Flavoring Chemicals Induce Cytotoxicity
in HepG2 Cells |
title_sort | e-cigarette flavoring chemicals induce cytotoxicity
in hepg2 cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970492/ https://www.ncbi.nlm.nih.gov/pubmed/33748584 http://dx.doi.org/10.1021/acsomega.0c05639 |
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