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Modeled Respiratory Tract Deposition of Aerosolized Oil Diluents Used in Δ(9)-THC-Based Electronic Cigarette Liquid Products

Electronic cigarette, or vaping, products (EVP) heat liquids (“e-liquids”) that contain substances (licit or illicit) and deliver aerosolized particles into the lungs. Commercially available oils such as Vitamin-E-acetate (VEA), Vitamin E oil, coconut, and medium chain triglycerides (MCT) were often...

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Autores principales: Ranpara, Anand, Stefaniak, Aleksandr B., Williams, Kenneth, Fernandez, Elizabeth, LeBouf, Ryan F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599147/
https://www.ncbi.nlm.nih.gov/pubmed/34805068
http://dx.doi.org/10.3389/fpubh.2021.744166
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author Ranpara, Anand
Stefaniak, Aleksandr B.
Williams, Kenneth
Fernandez, Elizabeth
LeBouf, Ryan F.
author_facet Ranpara, Anand
Stefaniak, Aleksandr B.
Williams, Kenneth
Fernandez, Elizabeth
LeBouf, Ryan F.
author_sort Ranpara, Anand
collection PubMed
description Electronic cigarette, or vaping, products (EVP) heat liquids (“e-liquids”) that contain substances (licit or illicit) and deliver aerosolized particles into the lungs. Commercially available oils such as Vitamin-E-acetate (VEA), Vitamin E oil, coconut, and medium chain triglycerides (MCT) were often the constituents of e-liquids associated with an e-cigarette, or vaping, product use-associated lung injury (EVALI). The objective of this study was to evaluate the mass-based physical characteristics of the aerosolized e-liquids prepared using these oil diluents. These characteristics were particle size distributions for modeling regional respiratory deposition and puff-based total aerosol mass for estimating the number of particles delivered to the respiratory tract. Four types of e-liquids were prepared by adding terpenes to oil diluents individually: VEA, Vitamin E oil, coconut oil, and MCT. A smoking machine was used to aerosolize each e-liquid at a predetermined puff topography (volume of 55 ml for 3 s with 30-s intervals between puffs). A cascade impactor was used to collect the size-segregated aerosol for calculating the mass median aerodynamic diameter (MMAD) and geometric standard deviation (GSD). The respiratory deposition of EVP aerosols on inhalation was estimated using the Multiple-Path Particle Dosimetry model. From these results, the exhaled fraction of EVP aerosols was calculated as a surrogate of secondhand exposure potential. The MMAD of VEA (0.61 μm) was statistically different compared to MCT (0.38 μm) and coconut oil (0.47 μm) but not to Vitamin E oil (0.58 μm); p < 0.05. Wider aerosol size distribution was observed for VEA (GSD 2.35) and MCT (GSD 2.08) compared with coconut oil (GSD 1.53) and Vitamin E oil (GSD 1.55). Irrespective of the statistical differences between MMADs, dosimetry modeling resulted in the similar regional and lobular deposition of particles for all e-liquids in the respiratory tract. The highest (~0.08 or more) fractional deposition was predicted in the pulmonary region, which is consistent as the site of injury among EVALI cases. Secondhand exposure calculations indicated that a substantial amount of EVP aerosols could be exhaled, which has potential implications for bystanders. The number of EVALI cases has declined with the removal of VEA; however, further research is required to investigate the commonly available commercial ingredients used in e-liquid preparations.
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spelling pubmed-85991472021-11-19 Modeled Respiratory Tract Deposition of Aerosolized Oil Diluents Used in Δ(9)-THC-Based Electronic Cigarette Liquid Products Ranpara, Anand Stefaniak, Aleksandr B. Williams, Kenneth Fernandez, Elizabeth LeBouf, Ryan F. Front Public Health Public Health Electronic cigarette, or vaping, products (EVP) heat liquids (“e-liquids”) that contain substances (licit or illicit) and deliver aerosolized particles into the lungs. Commercially available oils such as Vitamin-E-acetate (VEA), Vitamin E oil, coconut, and medium chain triglycerides (MCT) were often the constituents of e-liquids associated with an e-cigarette, or vaping, product use-associated lung injury (EVALI). The objective of this study was to evaluate the mass-based physical characteristics of the aerosolized e-liquids prepared using these oil diluents. These characteristics were particle size distributions for modeling regional respiratory deposition and puff-based total aerosol mass for estimating the number of particles delivered to the respiratory tract. Four types of e-liquids were prepared by adding terpenes to oil diluents individually: VEA, Vitamin E oil, coconut oil, and MCT. A smoking machine was used to aerosolize each e-liquid at a predetermined puff topography (volume of 55 ml for 3 s with 30-s intervals between puffs). A cascade impactor was used to collect the size-segregated aerosol for calculating the mass median aerodynamic diameter (MMAD) and geometric standard deviation (GSD). The respiratory deposition of EVP aerosols on inhalation was estimated using the Multiple-Path Particle Dosimetry model. From these results, the exhaled fraction of EVP aerosols was calculated as a surrogate of secondhand exposure potential. The MMAD of VEA (0.61 μm) was statistically different compared to MCT (0.38 μm) and coconut oil (0.47 μm) but not to Vitamin E oil (0.58 μm); p < 0.05. Wider aerosol size distribution was observed for VEA (GSD 2.35) and MCT (GSD 2.08) compared with coconut oil (GSD 1.53) and Vitamin E oil (GSD 1.55). Irrespective of the statistical differences between MMADs, dosimetry modeling resulted in the similar regional and lobular deposition of particles for all e-liquids in the respiratory tract. The highest (~0.08 or more) fractional deposition was predicted in the pulmonary region, which is consistent as the site of injury among EVALI cases. Secondhand exposure calculations indicated that a substantial amount of EVP aerosols could be exhaled, which has potential implications for bystanders. The number of EVALI cases has declined with the removal of VEA; however, further research is required to investigate the commonly available commercial ingredients used in e-liquid preparations. Frontiers Media S.A. 2021-11-04 /pmc/articles/PMC8599147/ /pubmed/34805068 http://dx.doi.org/10.3389/fpubh.2021.744166 Text en Copyright © 2021 Ranpara, Stefaniak, Williams, Fernandez and LeBouf. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Ranpara, Anand
Stefaniak, Aleksandr B.
Williams, Kenneth
Fernandez, Elizabeth
LeBouf, Ryan F.
Modeled Respiratory Tract Deposition of Aerosolized Oil Diluents Used in Δ(9)-THC-Based Electronic Cigarette Liquid Products
title Modeled Respiratory Tract Deposition of Aerosolized Oil Diluents Used in Δ(9)-THC-Based Electronic Cigarette Liquid Products
title_full Modeled Respiratory Tract Deposition of Aerosolized Oil Diluents Used in Δ(9)-THC-Based Electronic Cigarette Liquid Products
title_fullStr Modeled Respiratory Tract Deposition of Aerosolized Oil Diluents Used in Δ(9)-THC-Based Electronic Cigarette Liquid Products
title_full_unstemmed Modeled Respiratory Tract Deposition of Aerosolized Oil Diluents Used in Δ(9)-THC-Based Electronic Cigarette Liquid Products
title_short Modeled Respiratory Tract Deposition of Aerosolized Oil Diluents Used in Δ(9)-THC-Based Electronic Cigarette Liquid Products
title_sort modeled respiratory tract deposition of aerosolized oil diluents used in δ(9)-thc-based electronic cigarette liquid products
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599147/
https://www.ncbi.nlm.nih.gov/pubmed/34805068
http://dx.doi.org/10.3389/fpubh.2021.744166
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