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Triacetin Enhances Levels of Acrolein, Formaldehyde Hemiacetals, and Acetaldehyde in Electronic Cigarette Aerosols
[Image: see text] The health effects of inhaled electronic cigarette (e-cigarette) flavoring compounds are largely unknown. Earlier reports of their chemical reactivity have been conflicting, with some claiming, for example, that the degradation of flavoring chemicals in e-cigarettes to aldehydes is...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068691/ https://www.ncbi.nlm.nih.gov/pubmed/30087908 http://dx.doi.org/10.1021/acsomega.8b00842 |
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author | Vreeke, Shawna Peyton, David H. Strongin, Robert M. |
author_facet | Vreeke, Shawna Peyton, David H. Strongin, Robert M. |
author_sort | Vreeke, Shawna |
collection | PubMed |
description | [Image: see text] The health effects of inhaled electronic cigarette (e-cigarette) flavoring compounds are largely unknown. Earlier reports of their chemical reactivity have been conflicting, with some claiming, for example, that the degradation of flavoring chemicals in e-cigarettes to aldehydes is statistically insignificant. It is thus important to understand how these molecules react to afford enhanced aerosol products. The purpose of the current study was to investigate the origin of formaldehyde, acrolein, and acetaldehyde in e-cigarettes that contain the popular additive, triacetin (TA). By using (13)C labeling and a combination of (1)H NMR and (13)C NMR, we were able to identify that ester hydrolysis of TA occurs to form acetic acid (HOAc) during aerosolization. The released HOAc acts as a catalyst in the degradation of propylene glycol (PG) and glycerol (GLY), increasing the formation of formaldehyde hemiacetals, acrolein, and acetaldehyde. A solution of 10% TA in 1:1 PG/GLY e-liquid was aerosolized using two different e-cigarettes at two wattages. Each device exhibited a significant increase in aldehyde levels, of up to 185% compared to the aerosol from a 1:1 PG/GLY e-liquid. In addition, the GLY formaldehyde hemiacetal was more predominant within the presence of HOAc, indicating that GLY may be relatively more prone to degradation from protonation. |
format | Online Article Text |
id | pubmed-6068691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60686912018-08-05 Triacetin Enhances Levels of Acrolein, Formaldehyde Hemiacetals, and Acetaldehyde in Electronic Cigarette Aerosols Vreeke, Shawna Peyton, David H. Strongin, Robert M. ACS Omega [Image: see text] The health effects of inhaled electronic cigarette (e-cigarette) flavoring compounds are largely unknown. Earlier reports of their chemical reactivity have been conflicting, with some claiming, for example, that the degradation of flavoring chemicals in e-cigarettes to aldehydes is statistically insignificant. It is thus important to understand how these molecules react to afford enhanced aerosol products. The purpose of the current study was to investigate the origin of formaldehyde, acrolein, and acetaldehyde in e-cigarettes that contain the popular additive, triacetin (TA). By using (13)C labeling and a combination of (1)H NMR and (13)C NMR, we were able to identify that ester hydrolysis of TA occurs to form acetic acid (HOAc) during aerosolization. The released HOAc acts as a catalyst in the degradation of propylene glycol (PG) and glycerol (GLY), increasing the formation of formaldehyde hemiacetals, acrolein, and acetaldehyde. A solution of 10% TA in 1:1 PG/GLY e-liquid was aerosolized using two different e-cigarettes at two wattages. Each device exhibited a significant increase in aldehyde levels, of up to 185% compared to the aerosol from a 1:1 PG/GLY e-liquid. In addition, the GLY formaldehyde hemiacetal was more predominant within the presence of HOAc, indicating that GLY may be relatively more prone to degradation from protonation. American Chemical Society 2018-07-02 /pmc/articles/PMC6068691/ /pubmed/30087908 http://dx.doi.org/10.1021/acsomega.8b00842 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Vreeke, Shawna Peyton, David H. Strongin, Robert M. Triacetin Enhances Levels of Acrolein, Formaldehyde Hemiacetals, and Acetaldehyde in Electronic Cigarette Aerosols |
title | Triacetin Enhances Levels of Acrolein, Formaldehyde
Hemiacetals, and Acetaldehyde in Electronic Cigarette Aerosols |
title_full | Triacetin Enhances Levels of Acrolein, Formaldehyde
Hemiacetals, and Acetaldehyde in Electronic Cigarette Aerosols |
title_fullStr | Triacetin Enhances Levels of Acrolein, Formaldehyde
Hemiacetals, and Acetaldehyde in Electronic Cigarette Aerosols |
title_full_unstemmed | Triacetin Enhances Levels of Acrolein, Formaldehyde
Hemiacetals, and Acetaldehyde in Electronic Cigarette Aerosols |
title_short | Triacetin Enhances Levels of Acrolein, Formaldehyde
Hemiacetals, and Acetaldehyde in Electronic Cigarette Aerosols |
title_sort | triacetin enhances levels of acrolein, formaldehyde
hemiacetals, and acetaldehyde in electronic cigarette aerosols |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068691/ https://www.ncbi.nlm.nih.gov/pubmed/30087908 http://dx.doi.org/10.1021/acsomega.8b00842 |
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