Abstract:The current fourth generation (“pod-style”) electronic cigarette, or vaping, products (EVPs) heat a liquid (“e-liquid”) contained in a reservoir (“pod”) using a battery-powered coil to deliver aerosol into the lungs. A portion of inhaled EVP aerosol is estimated as exhaled, which can present a potential secondhand exposure risk to bystanders. The effects of modifiable factors using either a prefilled disposable or refillable pod-style EVPs on aerosol particle size distribution (PSD) and its respiratory deposit… Show more
“…The physical properties of the ENDS aerosol will be influenced by multiple factors, including e-liquid composition, ENDS device settings, and vaping topography. Aerosol density and size distribution will mainly determine pulmonary deposition along the respiratory tract, in addition to the aerosol also being partly exhaled [ 38 , 39 ]. Thus, the pulmonary absorption of the carbonyls found in the ENDS aerosols will be influenced, among others, by the chemical properties of the specific carbonyl, for instance, acrolein, acetaldehyde, and formaldehyde are primarily upper respiratory tract irritants [ 40 ]; the lung morphology, the lung disease state, the breathing pattern, as well as the ENDS aerosol particulate phase [ 38 , 39 ].…”
Section: Discussionmentioning
confidence: 99%
“…Aerosol density and size distribution will mainly determine pulmonary deposition along the respiratory tract, in addition to the aerosol also being partly exhaled [ 38 , 39 ]. Thus, the pulmonary absorption of the carbonyls found in the ENDS aerosols will be influenced, among others, by the chemical properties of the specific carbonyl, for instance, acrolein, acetaldehyde, and formaldehyde are primarily upper respiratory tract irritants [ 40 ]; the lung morphology, the lung disease state, the breathing pattern, as well as the ENDS aerosol particulate phase [ 38 , 39 ]. Whether the adsorption of carbonyls onto the ENDS aerosol particulate phase increases the distribution of these compounds in the lower respiratory tract (bronchial and alveolar regions) is currently unknow, and thus merit future investigation.…”
Propylene glycol (PG) and glycerin (G) are the most widely used humectants in electronic nicotine delivery system (ENDS) devices. Carbonyls are present in aerosols produced when ENDS devices heat PG and G. Whether aerosolized PG and G are innocuous to the lungs has not been established. Here, we determined the chemical profiles of ENDS aerosols containing three humectant ratios (30/70, 50/50 and 70/30, PG/VG), for three flavors (strawberry, vanilla and Catalan cream) containing either 12 or 18 mg/mL of nicotine. Additionally, we examined the in vitro toxicity of the strawberry- and vanilla-flavored ENDS aerosol in human lung epithelial cells (BEAS-2B) exposed at the air-liquid interface for 1 h. For strawberry- and vanilla-flavored aerosols produced by a 3rd-generation ENDS device with the same PG/G ratio, the e-liquid nicotine content of 12 and 18 mg/mL did not transfer to the aerosol with substantial differences in concentrations. Our data also indicate the presence of carbonyls in all three flavored e-cig aerosols analyzed, with levels exceeding 1 µg/puff for acetone, butyraldehyde, and acetaldehyde, in strawberry-, vanilla, and Catalan cream-flavored e-cig aerosols, respectively. Furthermore, closed-system ENDS of the fourth generation emitted trace levels of carbonyls in the aerosols (<0.3 µg/puff), while open-system tank-style ENDS of the third generation produced elevated levels of harmful chemicals, including acrolein (>1 µg/puff), formaldehyde (>5 µg/puff), and m- & p-tolualdehyde (>4 µg/puff). Moreover, under non-cytotoxic conditions, BEAS-2B cells exposed to strawberry-flavored aerosols exhibited significantly increased reactive oxygen and nitric oxide species (ROS/NOS) levels in cell media compared to air controls, while vanilla-flavored ENDS aerosols up-regulated the expression of pro-inflammatory and oxidative stress markers. Our data suggest (a) that ENDS aerosol chemical composition will vary based upon the presence and concentration of the initial e-liquid ingredients, with a pronounced impact of the flavoring components; and (b) short-term exposures to flavored ENDS aerosols may impair lung cells’ redox signaling in a flavor-specific manner.
“…The physical properties of the ENDS aerosol will be influenced by multiple factors, including e-liquid composition, ENDS device settings, and vaping topography. Aerosol density and size distribution will mainly determine pulmonary deposition along the respiratory tract, in addition to the aerosol also being partly exhaled [ 38 , 39 ]. Thus, the pulmonary absorption of the carbonyls found in the ENDS aerosols will be influenced, among others, by the chemical properties of the specific carbonyl, for instance, acrolein, acetaldehyde, and formaldehyde are primarily upper respiratory tract irritants [ 40 ]; the lung morphology, the lung disease state, the breathing pattern, as well as the ENDS aerosol particulate phase [ 38 , 39 ].…”
Section: Discussionmentioning
confidence: 99%
“…Aerosol density and size distribution will mainly determine pulmonary deposition along the respiratory tract, in addition to the aerosol also being partly exhaled [ 38 , 39 ]. Thus, the pulmonary absorption of the carbonyls found in the ENDS aerosols will be influenced, among others, by the chemical properties of the specific carbonyl, for instance, acrolein, acetaldehyde, and formaldehyde are primarily upper respiratory tract irritants [ 40 ]; the lung morphology, the lung disease state, the breathing pattern, as well as the ENDS aerosol particulate phase [ 38 , 39 ]. Whether the adsorption of carbonyls onto the ENDS aerosol particulate phase increases the distribution of these compounds in the lower respiratory tract (bronchial and alveolar regions) is currently unknow, and thus merit future investigation.…”
Propylene glycol (PG) and glycerin (G) are the most widely used humectants in electronic nicotine delivery system (ENDS) devices. Carbonyls are present in aerosols produced when ENDS devices heat PG and G. Whether aerosolized PG and G are innocuous to the lungs has not been established. Here, we determined the chemical profiles of ENDS aerosols containing three humectant ratios (30/70, 50/50 and 70/30, PG/VG), for three flavors (strawberry, vanilla and Catalan cream) containing either 12 or 18 mg/mL of nicotine. Additionally, we examined the in vitro toxicity of the strawberry- and vanilla-flavored ENDS aerosol in human lung epithelial cells (BEAS-2B) exposed at the air-liquid interface for 1 h. For strawberry- and vanilla-flavored aerosols produced by a 3rd-generation ENDS device with the same PG/G ratio, the e-liquid nicotine content of 12 and 18 mg/mL did not transfer to the aerosol with substantial differences in concentrations. Our data also indicate the presence of carbonyls in all three flavored e-cig aerosols analyzed, with levels exceeding 1 µg/puff for acetone, butyraldehyde, and acetaldehyde, in strawberry-, vanilla, and Catalan cream-flavored e-cig aerosols, respectively. Furthermore, closed-system ENDS of the fourth generation emitted trace levels of carbonyls in the aerosols (<0.3 µg/puff), while open-system tank-style ENDS of the third generation produced elevated levels of harmful chemicals, including acrolein (>1 µg/puff), formaldehyde (>5 µg/puff), and m- & p-tolualdehyde (>4 µg/puff). Moreover, under non-cytotoxic conditions, BEAS-2B cells exposed to strawberry-flavored aerosols exhibited significantly increased reactive oxygen and nitric oxide species (ROS/NOS) levels in cell media compared to air controls, while vanilla-flavored ENDS aerosols up-regulated the expression of pro-inflammatory and oxidative stress markers. Our data suggest (a) that ENDS aerosol chemical composition will vary based upon the presence and concentration of the initial e-liquid ingredients, with a pronounced impact of the flavoring components; and (b) short-term exposures to flavored ENDS aerosols may impair lung cells’ redox signaling in a flavor-specific manner.
“…There are additional issues meriting further consideration that need to be addressed in the context of the emerging products described herein. For example, user behaviour and how it changes from device to device impacting toxicant exposure, factors modulating particle size distributions,66 interlaboratory reproducibility of findings, the correlation of laboratory studies to realistic usage, the significance of secondhand and thirdhand smoke and the development of standardised laboratory methods67 are relevant issues 68. As the FDA continues to aggressively regulate tobacco products through the PMTA pathway and approves new ENDS to enter the market, tobacco researchers need to be vigilant and conduct research that supports regulatory actions to protect public health.…”
Electronic nicotine delivery systems (ENDS) continue to rapidly evolve. Current products pose unique challenges and opportunities for researchers and regulators. This commentary aims to highlight research gaps, particularly in toxicity research, and provide guidance on priority research questions for the tobacco regulatory community. Disposable flavoured ENDS have become the most popular device class among youth and may contain higher nicotine levels than JUUL devices. They also exhibit enhanced harmful and potentially harmful constituents production, contain elevated levels of synthetic coolants and pose environmental concerns. Synthetic nicotine and flavour capsules are innovations that have recently enabled the circumvention of Food and Drug Administration oversight. Coil-less ENDS offer the promise of delivering fewer toxicants due to the absence of heating coils, but initial studies show that these products exhibit similar toxicological profiles compared with JUULs. Each of these topic areas requires further research to understand and mitigate their impact on human health, especially their risks to young users.
“…As the popularity of the pod-type ENDS device gradually increases, safety concerns have escalated, warranting further examination of the hazards posed by pod-type ENDS-emitted aerosol exposures. Indeed, differential vaping patterns or levels of ENDS usage can contribute to exposure variances to various organic and inorganic hazards, including heavy metals [ 7 , 8 , 9 ]. Several metals have been detected in pod-type ENDS aerosols, such as chromium (Cr), nickel (Ni), copper (Cu), zinc (Zn), cadmium (Cd), tin (Sn), manganese (Mn), and lead (Pb) [ 10 , 11 ].…”
Section: Introductionmentioning
confidence: 99%
“…Increased metal exposure is a critical risk factor for various respiratory diseases, such as respiratory inflammation, asthma, COPD, and respiratory cancer [ 14 , 15 , 16 ]. However, there is a lack of evidence to determine the level of metal exposure from the pod-type ENDS aerosol because of the inconsistency of aerosol generation parameters, type of device, and e-liquid selection in recent studies [ 7 , 17 , 18 ]. Therefore, a detailed evaluation of the level of metal exposure derived from pod-type ENDS usage is needed to determine the potential adverse effects on respiratory health.…”
Electronic nicotine delivery systems (ENDS) aerosols are complex mixtures of chemicals, metals, and particles that may present inhalation hazards and adverse respiratory health risks. Despite being considered a safer alternative to tobacco cigarettes, metal exposure levels and respiratory effects associated with device aging and vaping frequency have not been fully characterized. In this study, we utilize an automated multi-channel ENDS aerosol generation system (EAGS) to generate aerosols from JUUL pod-type ENDS using tobacco-flavored e-liquid. Aerosol puff fractions (1–50) and (101–150) are monitored and sampled using various collection media. Extracted aerosols are prepared for metal and toxicological analysis using human primary small airway epithelial cells (SAEC). ENDS aerosol-mediated cellular responses, including reactive oxygen species (ROS), oxidative stress, cell viability, and DNA damage, are evaluated after 24 h and 7-day exposures. Our results show higher particle concentrations in later puff fractions (0.135 mg/m3) than in initial puff fractions (0.00212 mg/m3). Later puff fraction aerosols contain higher toxic metal concentrations, including chromium, copper, and lead, which elicit increased levels of ROS followed by significant declines in total glutathione and cell viability. Notably, a 30% increase in DNA damage was observed after 7 days because of later puff fraction exposures. This work is consistent with ENDS aerosols becoming more hazardous across the use of pre-filled pod devices, which may threaten respiratory health.
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