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Evaluation of e-liquid toxicity using an open-source high-throughput screening assay

The e-liquids used in electronic cigarettes (E-cigs) consist of propylene glycol (PG), vegetable glycerin (VG), nicotine, and chemical additives for flavoring. There are currently over 7,700 e-liquid flavors available, and while some have been tested for toxicity in the laboratory, most have not. He...

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Autores principales: Sassano, M. Flori, Davis, Eric S., Keating, James E., Zorn, Bryan T., Kochar, Tavleen K., Wolfgang, Matthew C., Glish, Gary L., Tarran, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870948/
https://www.ncbi.nlm.nih.gov/pubmed/29584716
http://dx.doi.org/10.1371/journal.pbio.2003904
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author Sassano, M. Flori
Davis, Eric S.
Keating, James E.
Zorn, Bryan T.
Kochar, Tavleen K.
Wolfgang, Matthew C.
Glish, Gary L.
Tarran, Robert
author_facet Sassano, M. Flori
Davis, Eric S.
Keating, James E.
Zorn, Bryan T.
Kochar, Tavleen K.
Wolfgang, Matthew C.
Glish, Gary L.
Tarran, Robert
author_sort Sassano, M. Flori
collection PubMed
description The e-liquids used in electronic cigarettes (E-cigs) consist of propylene glycol (PG), vegetable glycerin (VG), nicotine, and chemical additives for flavoring. There are currently over 7,700 e-liquid flavors available, and while some have been tested for toxicity in the laboratory, most have not. Here, we developed a 3-phase, 384-well, plate-based, high-throughput screening (HTS) assay to rapidly triage and validate the toxicity of multiple e-liquids. Our data demonstrated that the PG/VG vehicle adversely affected cell viability and that a large number of e-liquids were more toxic than PG/VG. We also performed gas chromatography–mass spectrometry (GC-MS) analysis on all tested e-liquids. Subsequent nonmetric multidimensional scaling (NMDS) analysis revealed that e-liquids are an extremely heterogeneous group. Furthermore, these data indicated that (i) the more chemicals contained in an e-liquid, the more toxic it was likely to be and (ii) the presence of vanillin was associated with higher toxicity values. Further analysis of common constituents by electron ionization revealed that the concentration of cinnamaldehyde and vanillin, but not triacetin, correlated with toxicity. We have also developed a publicly available searchable website (www.eliquidinfo.org). Given the large numbers of available e-liquids, this website will serve as a resource to facilitate dissemination of this information. Our data suggest that an HTS approach to evaluate the toxicity of multiple e-liquids is feasible. Such an approach may serve as a roadmap to enable bodies such as the Food and Drug Administration (FDA) to better regulate e-liquid composition.
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spelling pubmed-58709482018-04-06 Evaluation of e-liquid toxicity using an open-source high-throughput screening assay Sassano, M. Flori Davis, Eric S. Keating, James E. Zorn, Bryan T. Kochar, Tavleen K. Wolfgang, Matthew C. Glish, Gary L. Tarran, Robert PLoS Biol Methods and Resources The e-liquids used in electronic cigarettes (E-cigs) consist of propylene glycol (PG), vegetable glycerin (VG), nicotine, and chemical additives for flavoring. There are currently over 7,700 e-liquid flavors available, and while some have been tested for toxicity in the laboratory, most have not. Here, we developed a 3-phase, 384-well, plate-based, high-throughput screening (HTS) assay to rapidly triage and validate the toxicity of multiple e-liquids. Our data demonstrated that the PG/VG vehicle adversely affected cell viability and that a large number of e-liquids were more toxic than PG/VG. We also performed gas chromatography–mass spectrometry (GC-MS) analysis on all tested e-liquids. Subsequent nonmetric multidimensional scaling (NMDS) analysis revealed that e-liquids are an extremely heterogeneous group. Furthermore, these data indicated that (i) the more chemicals contained in an e-liquid, the more toxic it was likely to be and (ii) the presence of vanillin was associated with higher toxicity values. Further analysis of common constituents by electron ionization revealed that the concentration of cinnamaldehyde and vanillin, but not triacetin, correlated with toxicity. We have also developed a publicly available searchable website (www.eliquidinfo.org). Given the large numbers of available e-liquids, this website will serve as a resource to facilitate dissemination of this information. Our data suggest that an HTS approach to evaluate the toxicity of multiple e-liquids is feasible. Such an approach may serve as a roadmap to enable bodies such as the Food and Drug Administration (FDA) to better regulate e-liquid composition. Public Library of Science 2018-03-27 /pmc/articles/PMC5870948/ /pubmed/29584716 http://dx.doi.org/10.1371/journal.pbio.2003904 Text en © 2018 Sassano et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Methods and Resources
Sassano, M. Flori
Davis, Eric S.
Keating, James E.
Zorn, Bryan T.
Kochar, Tavleen K.
Wolfgang, Matthew C.
Glish, Gary L.
Tarran, Robert
Evaluation of e-liquid toxicity using an open-source high-throughput screening assay
title Evaluation of e-liquid toxicity using an open-source high-throughput screening assay
title_full Evaluation of e-liquid toxicity using an open-source high-throughput screening assay
title_fullStr Evaluation of e-liquid toxicity using an open-source high-throughput screening assay
title_full_unstemmed Evaluation of e-liquid toxicity using an open-source high-throughput screening assay
title_short Evaluation of e-liquid toxicity using an open-source high-throughput screening assay
title_sort evaluation of e-liquid toxicity using an open-source high-throughput screening assay
topic Methods and Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870948/
https://www.ncbi.nlm.nih.gov/pubmed/29584716
http://dx.doi.org/10.1371/journal.pbio.2003904
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