Esther E Omaiye1,2, Wentai Luo3,4, Kevin J McWhirter3, James F Pankow3,4, Prue Talbot2. 1. Environmental Toxicology Graduate Program, University of California Riverside, Riverside, California 92521, United States. 2. Department of Molecular, Cell, and Systems Biology, University of California Riverside, Riverside, California 92521, United States. 3. Department of Civil and Environmental Engineering, Portland State University, Portland, Oregon 97201, United States. 4. Department of Chemistry, Portland State University, Portland, Oregon 97201, United States.
Abstract
The popularity of disposable fourth-generation electronic cigarettes (ECs) among young adults and adolescents has been increasing since the ban on flavored cartridge EC products such as JUUL. Although the constituents and toxicity of some cartridge-based fourth-generation ECs, such as JUUL, have been studied, limited data exist for other disposable ECs such as Puff. The purpose of this study was to determine flavor chemicals, synthetic coolants, and nicotine concentrations in 16 disposable Puff devices, evaluate the cytotoxicity of the different flavors from the Puff brand using in vitro assays, and investigate the health risks of synthetic coolants in EC products. Gas chromatography/mass spectrometry was used to identify and quantify chemicals in Puff EC fluids. One hundred and twenty-six flavor chemicals were identified in Puff fluids, and 16 were >1 mg/mL. WS-23 (2-isopropyl-N,2,3-trimethylbutyramide) was present in all products, and concentrations ranged from 0.8 to 45.1 mg/mL. WS-3 (N-ethyl-p-menthane-3-carboxamide) concentrations ranged from 1.5 to 16.4 mg/mL in 6/16 products. Nicotine concentrations ranged from 40.6 to 52.4 (average 44.8 mg/mL). All unvaped fluids were cytotoxic at dilutions between 0.1 and 10% in the MTT and neutral red uptake assays when tested with BEAS-2B lung epithelial cells. The cytotoxicity of Puff fluids was highly correlated with total chemical concentrations, nicotine, WS-23, both synthetic coolants, and synthetic coolants plus ethyl maltol. Lower concentrations of WS-23 than those in the fluids adversely affected cell growth and morphology. Concentrations of synthetic coolants exceeded levels used in consumer products. The margin of exposure data showed that WS-3 and WS-23 concentrations were high enough in Puff products to present a health hazard. Our study demonstrates that disposable Puff ECs have high levels of cytotoxic chemicals. The data support the regulation of flavor chemicals and synthetic coolants in ECs to limit potentially harmful health effects.
The popularity of disposable fourth-generation electronic cigarettes (ECs) among young adults and adolescents has been increasing since the ban on flavored cartridge EC products such as JUUL. Although the constituents and toxicity of some cartridge-based fourth-generation ECs, such as JUUL, have been studied, limited data exist for other disposable ECs such as Puff. The purpose of this study was to determine flavor chemicals, synthetic coolants, and nicotine concentrations in 16 disposable Puff devices, evaluate the cytotoxicity of the different flavors from the Puff brand using in vitro assays, and investigate the health risks of synthetic coolants in EC products. Gas chromatography/mass spectrometry was used to identify and quantify chemicals in Puff EC fluids. One hundred and twenty-six flavor chemicals were identified in Puff fluids, and 16 were >1 mg/mL. WS-23 (2-isopropyl-N,2,3-trimethylbutyramide) was present in all products, and concentrations ranged from 0.8 to 45.1 mg/mL. WS-3 (N-ethyl-p-menthane-3-carboxamide) concentrations ranged from 1.5 to 16.4 mg/mL in 6/16 products. Nicotine concentrations ranged from 40.6 to 52.4 (average 44.8 mg/mL). All unvaped fluids were cytotoxic at dilutions between 0.1 and 10% in the MTT and neutral red uptake assays when tested with BEAS-2B lung epithelial cells. The cytotoxicity of Puff fluids was highly correlated with total chemical concentrations, nicotine, WS-23, both synthetic coolants, and synthetic coolants plus ethyl maltol. Lower concentrations of WS-23 than those in the fluids adversely affected cell growth and morphology. Concentrations of synthetic coolants exceeded levels used in consumer products. The margin of exposure data showed that WS-3 and WS-23 concentrations were high enough in Puff products to present a health hazard. Our study demonstrates that disposable Puff ECs have high levels of cytotoxic chemicals. The data support the regulation of flavor chemicals and synthetic coolants in ECs to limit potentially harmful health effects.
Electronic cigarettes (ECs), which contain
nicotine, solvents,
and flavor chemicals, continue to evolve and grow in popularity, especially
among young adults.[1−6] The popularity of fourth-generation EC products and their disposable
spinoffs, especially among young users, has been attributed to flavored
and “icy” fluids, usability, and device features that
facilitate stealth use.[7−12] EC fluids and aerosols generated from multiple devices contain higher
concentrations of chemicals than used in other consumer products,
such as foods, cosmetics, and medicines.[13−15] ECs and their
constituents are cytotoxic to cells, induce inflammatory responses,
increase oxidative stress, cause cellular senescence, and negatively
affect cell membrane channel potentials.[16−23] Despite concern over the use of flavor chemicals in ECs, the chemicals
used in EC fluids continue to change and are largely unregulated.
Even though JUUL dominates the EC market with 63% of current sales,[24,25] projections show that disposables, such as Puff Bar, are likely
to continue to increase their sales through 2028.[26]The technology used by manufacturers of fourth-generation
ECs,
such as JUUL and Puff Bar, is innovative. Nicotine is combined with
an acid(s) to reduce the amount of free-base nicotine, making the
resulting aerosol less harsh. The use of acids allows manufacturers
to increase nicotine concentrations (e.g., 61 mg/mL in JUUL)[27,28] while making it less harsh to users,[29−31] thereby increasing the
likelihood of addiction. To reduce sales of JUUL to young users, the
Food and Drug Administration (FDA) enacted a ban on cartridge-based
flavored EC pods in 2020.[32] Consumers and
suppliers quickly discovered a loophole in the ban, which did not
cover “disposable” flavored EC products, such as Puff
ECs.[33,34] The market for disposable pods continues
to grow, with dozens of products offered by multiple purveyors.[35,36]Although Puff ECs are the most widely used of the fourth-generation
disposable products, very little is known about their fluids’
chemical composition and toxicity. The purpose of our study was to
(1) identify and quantify nicotine, flavor chemicals, and synthetic
coolants in Puff fluids, (2) determine the toxicity of the Puff fluids
and WS-23 in multiple assays, (3) evaluate the transfer efficiency
of synthetic coolants to aerosols, and (4) perform (margin of exposure)
MOE risk assessment analysis on synthetic coolants in Puff products.
Materials and Methods
Materials
Isopropyl alcohol (IPA), Dulbecco’s
phosphate-buffered saline (DPBS), dimethyl sulfoxide (DMSO), ethanol
(EtOH), and acetic acid were purchased from Fisher Scientific (Chino,
CA). Analytical grade WS-3 (N-ethyl-p-menthane-3-carboxamide) (CAS # 39711-79-0; catalog #E0796; Lot:
SYXVH-SP) and WS-23 (2-isopropyl-N,2,3-trimethylbutyramide)
(CAS # 51115-67-4; catalog #I0729; Lot: LTNPJ-DP) both >98% pure
were
purchased from Tokyo Chemical Industry Co. LTD. (Portland, OR). BEAS-2B
cells were obtained from American Type Cell Culture (ATCC, Manassas,
VA). Bronchial epithelial basal medium (BEBM) and supplements were
purchased from Lonza (Walkersville, MD). Collagen (30 mg/mL), bovine
serum albumin (BSA, 10 mg/mL), fibronectin (10 mg/mL), poly-vinyl-pyrrolidone
(PVP), MTT reagent (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium
bromide), NRU dye (neutral red uptake dye), Tris-HCl, Tris-base, lithium
lactate, tetrazolium salt (INT), phenazine methosulfate (PMS), and
β-nicotinamide adenine dinucleotide (NAD) sodium salt were purchased
from Sigma-Aldrich (St Louis, MO).
Sample Acquisition
Sixteen disposable Puff EC devices
were purchased from vape shops in Los Angeles, CA, and Riverside,
CA, in 2020. Twelve Puff Bar flavors (“Tobacco,” “Grape,”
“Pomegranate,” “Cucumber,” “Café
Latte,” “Tangerine Ice,” “Peach Ice,”
“Banana Ice,” “Sour Apple,” “Melon
Ice,” “Menthol,” and “no flavor”
(“Clear”)) were labeled to contain 1.3 mL of fluids
and advertised to deliver 300 puffs/device. Four Puff Plus flavors
(“Mixed Berries,” “Aloe Grape,” “Cool
Mint,” and “Lychee Ice”) were labeled to contain
3.2 mL of fluids and advertised to deliver 800 puffs/device. All devices
were inventoried, stored in the dark at room temperature, and analyzed
within 2–3 weeks of purchase.Authentic standards of
both WS-3 and WS-23 were dissolved in propylene glycol (PG, 80%) and
distilled water (<20%) to simulate lab-made refill fluids. A PG
control blank was prepared with 80% PG and 20% distilled water.
Aerosol Production and Capture Using an Impinger Method
The transfer efficiency of synthetic coolants from lab-made fluids
into the aerosols was evaluated using a fourth-generation Baton V2
open pod system equipped with a 350 mAh rechargeable battery, a 1.5
mL refillable pod, and a 1.6 Ω coil that produces an aerosol
at 3.7 V/8.6 W. Refillable pods were filled with lab-made fluids and
preconditioned by taking three puffs before making aerosol solutions.
The generated aerosol was bubbled through and captured in IPA for
chemical analysis. The WS-3 and WS-23 aerosol materials captured in
IPA (referred to as “aerosol”) were collected at room
temperature in two tandem 125 mL impingers, each containing 25 mL
of IPA. The Baton V2 pod system was connected to a Cole-Parmer Masterflex
L/S peristaltic pump and was puffed using a 4.3 s puff duration,[21] interpuff intervals of 60 s, and an airflow
rate of 10–13 mL/s. To reduce the likelihood of “dry
puffing,” the fluid level was monitored, and the device was
not vaped beyond 3/4 of the pod. The pods were weighed before and
after aerosol production to collect at least 10 mg for gas chromatography/mass
spectrometry (GC/MS) analysis. Aerosol solutions were stored at −20
°C until shipped to Portland State University for analysis.
Gas Chromatography/Mass Spectrometry
Puff ECs containing
fluid-saturated wicks were dissected to expose the atomizers. The
fluid-saturated wicks were centrifuged in Qiagen MinElute spin columns
(Valencia, CA) at 3000 rpm for 3 min to separate the fluid from the
wick. The extracted fluid was analyzed using previously described
GC/MS methods.[28,37] Each sample (50 μL) was
dissolved in 0.95 mL of IPA and shipped overnight on ice to Portland
State University, where they were analyzed on the day they were received.
A 20 μL aliquot of internal standard solution (2000 ng/μL
of 1,2,3-trichlorobenzene dissolved in IPA) was added to each diluted
sample before analysis. Using internal-standard-based calibration
procedures described elsewhere,[37] analyses
for 178 flavor-related target analytes, two synthetic coolants, and
nicotine were performed with an Agilent 5975C GC/MS system (Santa
Clara, CA). A Restek Rxi-624Sil MS column (Bellefonte, PA) was used
(30 m long, 0.25 mm id, and 1.4 μm film thickness). A 1.0 μL
aliquot of the diluted sample was injected into the GC with a 10:1
split. The injector temperature was 235 °C. The GC temperature
program for analyses was 40 °C hold for 2 min, 10 °C/min
to 100 °C, then 12 °C/min to 280 °C and hold for 8
min at 280 °C, and then 10 °C/min to 230 °C. The MS
was operated in the electron impact ionization mode at 70 eV in the
positive-ion mode. The ion source temperature was 220 °C, and
the quadrupole temperature was 150 °C. The scan range was 34
to 400 amu. Each of the 181 (178 flavor chemicals, 2 synthetic coolants,
and nicotine) target analytes was quantitated using the authentic
standard material.In October 2019, two synthetic coolants (WS-3
and WS-23) and triethyl citrate were added to our GC/MS target list,
which is used to identify and quantify flavor chemicals. GC/MS data
collected for multiple EC libraries from 2016 to September 2019 were
re-evaluated to estimate the concentrations of synthetic coolants
(WS-3 and WS-23) and triethyl citrate using the average response factors
generated for them between October 2019 and December 2019.
Human Bronchial Epithelial Cells (BEAS-2B)
Experiments
were performed using BEAS-2B cells (passages 20–34), often
used for toxicological testing. BEAS-2B cells exposed to menthol in
submerged culture gave similar results to 3D EpiAirway exposed at
the air-liquid interface[38] and therefore
represent a good cell type for initiating work on the synthetic coolants.
BEAS-2B cells were cultured in bronchial epithelial growth medium
(BEGM) supplemented with 2 mL of the bovine pituitary extract and
0.5 mL each of insulin, hydrocortisone, retinoic acid, transferrin,
triiodothyronine, epinephrine, and human recombinant epidermal growth
factor. Nunc T-25 tissue culture flasks were coated overnight with
BEBM fortified with collagen (30 mg/mL), BSA (10 mg/mL), and fibronectin
(10 mg/mL) before culturing. Cells were maintained at 30–90%
confluence at 37 °C in a humidified incubator with 5% carbon
dioxide. For subculturing, cells were harvested using DPBS for washing
and incubated with 1.5 mL of 0.25% trypsin EDTA/DPBS and PVP for 3–4
min at 37 °C to allow detachment. Cells were counted using a
hemocytometer and cultured in T-25 flasks at 75,000 cells/flask. The
medium was replaced the next day and then every other day.For
in vitro assays, cells were cultured and harvested at 80–90%
confluency, using protocols previously described.[15] For the MTT, NRU, and LDH (lactate dehydrogenase) assays,
cells were plated at 10,000 cells/well in precoated 96-well plates
and allowed to attach overnight before a 24 h treatment. BEAS-2B cells
were plated at 42,000 cells/well in precoated 24-well plates for the
live-cell imaging experiments.
Cytotoxicity and Cell Viability Assays
The effects
of Puff fluids on the activity of mitochondrial reductase, neutral
red uptake, and LDH release were evaluated. In the culture medium,
serial dilutions of EC fluids (10, 3, 1, 0.3, 0.1, and 0.03%) were
arranged in 96-well plates with negative controls (0%) placed next
to the highest and lowest concentrations to check for avapor effect.[39] BEAS-2B cells were seeded and allowed to attach
for 24 h. Cells were exposed to treatments for 24 h before the MTT,
NRU, and LDH assays were performed.The MTT assay measures the
activity of mitochondrial reductases, which convert water-soluble
MTT salt to a formazan that accumulates in viable cells. After treatment,
20 μL of the MTT reagent (5 mg/mL) dissolved in DPBS were added
to wells and incubated for 2 h at 37 °C. Solutions were removed
from wells, and 100 μL of DMSO was added to each well and gently
mixed on a shaker to solubilize formazan crystals. Absorbance readings
of control and treated wells were taken against a DMSO blank at 570
nm using an Biotek Synergy HTX multi-mode reader (Santa Clara, CA).The NRU assay measures the uptake of neutral red dye, which accumulates
within the lysosomes of viable cells. Following the exposure of cells
to treatments, all medium was removed. A working solution of 40 μg
of neutral red stock/mL of cell culture medium was prepared and incubated
at 37 °C overnight to dissolve the neutral red. Cells were incubated
with 150 μL of neutral red solution for 2 h. Cells were washed
with PBS, and 150 μL of lysis buffer (50% EtOH/49% deionized
H2O/1% acetic acid) was added to each well and gently mixed to achieve
complete dissolution. Absorbance readings of wells were recorded at
540 nm using a Biotek Synergy HTX multi-mode reader.The LDH
assay measures lactate dehydrogenase released into the
culture medium due to plasma membrane damage. Reagents and solutions
were prepared using an in-house recipe developed by OPS Diagnostics
(Lebanon, NJ). TRIS (200 mM; 22.2 g of Tris-HCl, 10.6 g of Tris-base,
and 50 mM lithium lactate) at a pH of 8 was prepared in water. INT
was dissolved in DMSO (33 mg/mL), PMS was dissolved in water (9 mg/mL),
and NAD sodium salt was dissolved in water (3.7 mg/mL). The three
reagents (INT, PMS, and NAD) were combined to make the INT/PMS/NAD
solution. All reagents (50 μL) were added to empty wells, followed
by 50 μL of medium from treated and control wells. Absorbance
readings were recorded at 540 and 620 nm using a Biotek Synergy HTX
multi-mode reader.
Growth and Morphology Assays
Noninvasive cell growth
and morphology analyses of live cells were performed using 10×
and 20× phase contrast objectives in a BioStation CT using the
automatic Z-focus.[40] After attachment,
BEAS-2B cells were treated with Puff EC fluids (0.1–10%) or
with WS-23 (0.045–4.5 mg/mL) solutions dissolved in cell culture
medium. Images were taken every 2 h for 48 h to collect time-lapse
data for analysis. Evaluation of BEAS-2B growth and morphology was
compared in control and treated groups using Nikon CL Quant software
(Melville, NY).[40−42] Data from the treated groups were normalized to untreated
controls.
Solubility of WS-23 and WS-3 in Water and Culture Medium
WS-23 was dissolved in molecular grade water or culture medium at
concentrations of 0.45, 4.5, 7, or 9 mg/mL, and 500 μL of each
solution were added to 48-well plates with a glass bead in each well
to aid in focusing the liquid with a stereoscopic microscope. For
WS-3, 0.02 mg/mL was dissolved in water and cell culture medium to
confirm its reported solubility. Images were taken with a stereoscopic
microscope, and the presence of residues was compared for both solvents.
Statistical Analyses
For GC/MS data, data points are
averages of measurements from fluids obtained from three devices.
All values below the limit of quantification (LOQ) were excluded from
the data. Cytotoxicity analyses were performed using three different
cell passages, and each experiment was carried out at least three
times. Data were statistically analyzed with a one-way analysis of
variance (ANOVA). When significance was found (p <
0.05), each concentration was compared to the untreated control with
Dunnett’s post-hoc test using GraphPad Prism software (San
Diego, CA).
Results
Total Concentrations of Nicotine and Flavor Chemicals
Based on flavor names, Puff ECs were grouped into five categories:
tobacco, fruity, berries, menthol, and unflavored. The concentrations
of nicotine, flavor chemicals, synthetic coolants, and solvents were
analyzed (Figure ).
The average nicotine concentration in disposable Puff devices (44.8
mg/mL ± 2.5 SD) was lower than that in previously evaluated JUUL
pods (61 mg/mL), but higher than that in the cartomizer and refill
fluids we have examined[28] (Figure a). The total concentration
of flavor chemicals in Puff fluids was highly variable and ranged
from 0.7 (Cucumber) to 34.3 (Tobacco) mg/mL (Figure a). Fruit-flavored products were highly variable
in total concentrations and dominant chemicals (>1 mg/mL). Seven
flavor
chemicals, including ethyl maltol and ethyl acetate in Aloe Grape,
accounted for 80% of the sum of flavor chemicals. Minty flavored Puff
ECs contained two dominant flavor chemicals: menthol and p-Menthone in “Cool Mint” and triacetin in “Menthol.”
Although “Lychee Ice” and “Melon Ice”
contained only ethyl maltol as the dominant flavor chemical, “Peach
Ice” and “Clear” contained γ-undecalactone
and menthol, respectively.
Figure 1
Chemical concentrations in Puff EC fluids. (a)
Total flavor chemicals
ranged from 0.7 to 34.3 mg/mL, and nicotine concentrations ranged
from 41.2 to 52.3 mg/mL. (b) WS-3 and WS-23 concentrations ranged
from 1.5 to 15.5 and 0.9 to 35.9 mg/mL, respectively. The x-axis is sorted by increasing total flavor chemical concentration
and WS-23 in (a,b). Yellow bars in (b) indicate equal levels of synthetic
coolants. (c) PG and G concentrations ranged from 158 to 371 and 310
to 437 mg/mL, respectively. (d) Percentage of each chemical class
of chemicals in Puff products: flavor chemicals = 0.1–4.2%,
synthetic coolants = 0.1−5.6%, nicotine = 5.5–7.1%,
and solvents = 86.7–92.9%. (e) Heat map of individual flavor
chemicals ordered on the y-axis according to the
frequency of occurrence of dominant flavor chemicals. Products are
ranked according to decreasing total weight (mg/mL) of the flavor
chemicals on the x-axis from left to right. “PP”
on the flavor name on the x-axis indicates “Puff
Plus” products. Graphs show the means ± the standard deviation
of three independent measurements (n = 3), except
for “Sour Apple,” “Pomegranate,” and “Café
Latte,” which are each based on one measurement.
Chemical concentrations in Puff EC fluids. (a)
Total flavor chemicals
ranged from 0.7 to 34.3 mg/mL, and nicotine concentrations ranged
from 41.2 to 52.3 mg/mL. (b) WS-3 and WS-23 concentrations ranged
from 1.5 to 15.5 and 0.9 to 35.9 mg/mL, respectively. The x-axis is sorted by increasing total flavor chemical concentration
and WS-23 in (a,b). Yellow bars in (b) indicate equal levels of synthetic
coolants. (c) PG and G concentrations ranged from 158 to 371 and 310
to 437 mg/mL, respectively. (d) Percentage of each chemical class
of chemicals in Puff products: flavor chemicals = 0.1–4.2%,
synthetic coolants = 0.1−5.6%, nicotine = 5.5–7.1%,
and solvents = 86.7–92.9%. (e) Heat map of individual flavor
chemicals ordered on the y-axis according to the
frequency of occurrence of dominant flavor chemicals. Products are
ranked according to decreasing total weight (mg/mL) of the flavor
chemicals on the x-axis from left to right. “PP”
on the flavor name on the x-axis indicates “Puff
Plus” products. Graphs show the means ± the standard deviation
of three independent measurements (n = 3), except
for “Sour Apple,” “Pomegranate,” and “Café
Latte,” which are each based on one measurement.
Synthetic Coolants: WS-3 and WS-23
WS-3 and WS-23 were
identified and quantified in both “ice” and “nonice”
flavored Puff EC fluids (Figure b). WS-23 was present in all 16 products at concentrations
ranging from 0.8 mg/mL in “Tobacco” to 45.1 mg/mL in
“Cool Mint.” The levels of both synthetic coolants in
“Cucumber” and “Menthol” were similar
(5.1 and 4.3 mg/mL, respectively) and are shown using yellow bars
in Figure b. WS-3
concentrations in 6/16 products were generally lower than WS-23 ranging
from 1.5 mg/mL in “Tangerine Ice” to 16.4 mg/mL in “Clear”
(Figure b). The concentrations
of WS-3 in “Banana Ice,” “Mixed Berries,”
and “Café Latte” were below the LOQ (0.02 mg/mL).
The combined concentrations of WS-3 and WS-23 in products that contained
both synthetic coolants ranged from 0.9 to 55.8 mg/mL.EC products
purchased and analyzed between 2016 and 2019 were re-evaluated to
identify and estimate the concentrations of WS-3 and WS-23 in cartomizers,
pods, and refill fluids (Table S1). Out
of over 600 EC samples analyzed in our lab, both synthetic coolants
were found in 13 products: WS-3 (n = 5) and WS-23
(n = 8) (Table S3). The
concentrations of the synthetic coolants ranged from 0.2 to 1.7 mg/mL
for WS-3 and 0.1 to 3.9 mg/mL for WS-23. Triethyl citrate was more
frequently found in refill fluids at elevated levels and ranged from
0.05 to 11.5 mg/mL (Table S3).
PG and Glycerol Concentrations
All Puff EC fluids contained
PG and glycerol (G). The concentrations ranged from 158 to 371 and
310 to 437 mg of solvent/mL of undiluted Puff EC fluid for PG and
G, respectively (Figure c). The sum of both solvents in Puff ECs ranged from 544 to 740 mg/mL.
The percentage ratio of PG: G was approximately 30:70 in one product,
40:60 in three products, and 50:50 in 12 products (Figure c).
Contributions of Chemicals to the Total Sum of Chemicals in
Each Product
Chemicals in Puff ECs were grouped into four
categories: nicotine, synthetic coolants (WS-3 and WS-23), flavor
chemicals, and solvents (PG and G) (Figure d), and the percentage contribution of each
group to the total sum of chemicals was calculated. Nicotine accounted
for 5% of the total content in “Aloe Grape” to 7% in
“Tangerine Ice,” “Sour Apple,” and “Café
Latte.” The remaining 12 products contained 6% nicotine (Figure d). Synthetic coolant
contribution to the total chemicals ranged from 0.1% in “Tobacco”
to 6% in “Cool Mint” and “Clear” (unflavored
product). In 75% of the products, synthetic coolant concentration
to the total content was greater than 1% (Figure d). Flavor chemicals contributed between
0.09 and 4.2%, with more than half of the products higher than 1%.
Solvents accounted for the most chemicals ranging from 87% in “Cool
Mint” to 93% in “Cucumber.”
Individual Flavor Chemicals in Puff Bar Fluids
Seventy-one
percent (129/181) of the chemicals on our target analyte list were
identified in Puff EC fluids. Forty-two flavor chemicals detected
below the LOQ are listed in Table S2. Further
analysis was performed on 87 flavor chemicals above the LOQ (Figures e and S1). Except for “Sour Apple,” “Tangerine
Ice,” and “Cucumber,” all Puff ECs had at least
one dominant flavor chemical (>1 mg/mL) (Figure e). Ethyl maltol, menthol, vanillin, ethyl
propionate, ethyl butanoate, triacetin, methyl anthranilate, and (3Z)-3-hexen-1-ol were present in at least two products at
>1 mg/mL. p-Menthone, ethyl lactate, corylone,
isoamyl
acetate, benzyl alcohol, ethyl acetate, ethyl vanillin, and γ-undecalactone
were present in one product at >1 mg/mL. The concentrations of
dominant
flavor chemicals varied between Puff EC flavors and ranged from 1
to 15 mg/mL. Ethyl maltol was >1 mg/mL in 50% of the products evaluated.
Less dominant flavor chemicals (0.02–0.99 mg/mL) are shown
in Figure S1. While the frequency of all
chemicals detected ranged from 1 to 16, the total number of chemicals
per product ranged from 4 to 40 (Figures e, S1 and Table S2).Major and minor nontarget chemicals were investigated for
all Puff EC flavors. Benzoic acid, acetic acid, 2-hydroxypropyl acetate,
1,2-propanediol-2-acetate, 2-hydroxypropane-1,3-diyl diacetate, and
glycerol 1,2-diacetate were identified as major nontarget compounds
(Table S3). Vanillin and ethyl vanillin
PG and G acetals were present as minor nontarget compounds in products
that contained ≥5 mg of each chemical/mL of fluid (Figure e and Table S3).
Cytotoxicity of Puff EC Fluids
Cytotoxicity of Puff
EC fluids was evaluated with BEAS-2B cells using the MTT, NRU, and
LDH assays (Figure and Table ). Products
were considered cytotoxic if they had an effect of 30% less than the
untreated control (IC70).[43] Puff
EC fluids were cytotoxic in the MTT and NRU assays, and IC70 and IC50 values were reached at fluid concentrations
between 0.09–1.35 and 0.14–1.24%, respectively (Figure and Table ). Cell viability was evaluated
using the LDH assay, and no significant effects were observed (Figure a–p).
Figure 2
MTT, neutral
red, and LDH assay concentration–response curves
for BEAS-2B cells treated with Puff EC fluids. Purple line = MTT assay.
Red line = neutral red assay. Yellow line = LDH assay. The y-axis shows the response of cells in each assay as a percentage
of the untreated control. The concentrations tested were 0.03, 0.1,
0.3, 1, 3, and 10%. Each point is the mean ± standard error of
the mean of at least three independent experiments. Red and black
dotted lines on each graph represent IC70s and IC50s, respectively. For statistical significance, a = p < 0.05, b = p < 0.01, c = p < 0.001, and d = p < 0.0001.
Table 1
IC50s and IC70s for BEAS-2B Cells Treated with Puff EC Fluidsa
MTT (%)
NRU (%)
LDH (%)
refill fluids
IC50
IC70
IC50
IC70
IC50
IC70
Sour Appleb
0.15
0.09
-
-
-
-
Grape
0.33
0.18
0.64
0.35
>10
>10
Aloe Grape (PP)
0.51
0.22
0.41
0.19
>10
>10
Melon Ice
0.51
0.21
0.38
0.36
>10
>10
Lychee Ice (PP)
0.64
0.31
0.35
0.12
>10
>10
Mixed Berry (PP)
0.72
0.35
0.90
0.47
>10
>10
Clear
0.77
0.38
0.31
0.17
>10
>10
Cool Mint (PP)
0.75
0.41
0.42
0.20
>10
>10
Banana Ice
0.68
0.42
0.55
0.26
>10
>10
Tangerine Ice
0.67
0.44
0.57
0.30
>10
>10
Tobacco
0.80
0.46
0.67
0.34
>10
>10
Menthol
1.08
0.61
0.32
0.10
>10
>10
Café Latte
1.10
0.66
0.48
0.20
>10
>10
Peach Ice
1.11
0.66
1.04
0.49
>10
>10
Cucumber
1.24
0.67
0.55
0.21
>10
>10
Pomegranate
1.23
0.68
0.53
0.32
>10
>10
The highest concentration tested
was 1% of the EC refill fluids.
Sour Apple was not evaluated for
NRU and LDH.
MTT, neutral
red, and LDH assay concentration–response curves
for BEAS-2B cells treated with Puff EC fluids. Purple line = MTT assay.
Red line = neutral red assay. Yellow line = LDH assay. The y-axis shows the response of cells in each assay as a percentage
of the untreated control. The concentrations tested were 0.03, 0.1,
0.3, 1, 3, and 10%. Each point is the mean ± standard error of
the mean of at least three independent experiments. Red and black
dotted lines on each graph represent IC70s and IC50s, respectively. For statistical significance, a = p < 0.05, b = p < 0.01, c = p < 0.001, and d = p < 0.0001.The highest concentration tested
was 1% of the EC refill fluids.Sour Apple was not evaluated for
NRU and LDH.
Relationship between Chemical Concentrations and Cytotoxicity
Linear regressions were performed to determine the contributions
of nicotine, flavor chemicals, and synthetic coolants to the cytotoxicity
observed with Puff EC fluids (Figure ). The chemical concentrations and cytotoxicity data
for the 0.03–1% range were used to perform the regression analysis.
Regression coefficients (R2) for concentration
versus cytotoxicity were considered high (≥0.5), moderate (0.1–0.4),
or low (≤0.1). High and moderate correlations were observed
between cytotoxicity and concentrations of the total chemicals and
flavor chemicals (Figure a,b). The regression analysis for nicotine only, a combination
of synthetic coolants and WS-23, showed high and moderate correlations
with significant p-values (Figure c–e). WS-3 and ethyl maltol concentrations
were moderately correlated to cytotoxicity with significant p-values (Figure f,g). For products with both synthetic coolants and ethyl
maltol, the relationship between cytotoxicity and concentration was
high and statistically significant (Figure h). Regression analyses were performed for
all other dominant flavor chemicals (Figure S2). The correlation coefficients ranged from moderate (Figure S2a–k) to no relationship (Figure S2l–o) with almost no significant p-values.
Figure 3
Relationship between the toxicity of Puff EC fluids in
the MTT
assay and the chemical concentrations of nicotine, WS-3, WS-23, and
ethyl maltol in the Puff fluids. Linear regression analysis for cytotoxicity
in the MTT assays (y-axis, expressed as a percentage
of the untreated control) vs the concentrations of (a) total chemicals,
(b) total flavor chemicals, (c) nicotine only, (d) WS-3 and WS-23,
(e) WS-23 only, (f) WS-3 only, (g) ethyl maltol, and (h) synthetic
coolants and ethyl maltol. Toxicity was strongly correlated (R2 ≥ 0.5) with the total chemicals, nicotine
only, synthetic coolants, WS-23, and synthetic coolants and ethyl
maltol. Total flavor chemicals, WS-3, and ethyl maltol were moderately
correlated with toxicity (R2 < 0.5).
All correlations were significant (p < 0.05).
Linear regression analyses for toxicity vs other dominant flavor chemicals
are shown in Figure S2.
Relationship between the toxicity of Puff EC fluids in
the MTT
assay and the chemical concentrations of nicotine, WS-3, WS-23, and
ethyl maltol in the Puff fluids. Linear regression analysis for cytotoxicity
in the MTT assays (y-axis, expressed as a percentage
of the untreated control) vs the concentrations of (a) total chemicals,
(b) total flavor chemicals, (c) nicotine only, (d) WS-3 and WS-23,
(e) WS-23 only, (f) WS-3 only, (g) ethyl maltol, and (h) synthetic
coolants and ethyl maltol. Toxicity was strongly correlated (R2 ≥ 0.5) with the total chemicals, nicotine
only, synthetic coolants, WS-23, and synthetic coolants and ethyl
maltol. Total flavor chemicals, WS-3, and ethyl maltol were moderately
correlated with toxicity (R2 < 0.5).
All correlations were significant (p < 0.05).
Linear regression analyses for toxicity vs other dominant flavor chemicals
are shown in Figure S2.
Effect of WS-23 and Puff EC Fluids on Cell Growth and Morphology
Noninvasive analysis of BEAS-2B cell growth was performed using
time-lapse images taken over 48 h (Figure a–f). The typical epithelial monolayer
was observed for untreated control cells (Figure b,d,f). WS-23 significantly inhibited cell
growth in a concentration-dependent manner (Figure a,b). Significance was observed as early
as 20 h for cells treated with 10% (red lines), 28 h for 3% (blue
lines), 40 h for 1 and 0.3%, and 48 h for 0.1% fluid solutions (Figure a,b). Cells appeared
normal in all concentrations except in the 1.5 mg (3%) and 4.5 mg
(10%) treatments, where the cells appeared elongated and rounded,
respectively. Micrographs showing segmented images taken at 0, 24,
and 48 h are presented in Figures S3a.
Figure 4
Effects
of synthetic coolants and Puff EC fluids on cell growth
and morphology in the live-cell imaging assay. Time-lapse imaging
was performed with WS-23 (a,b), Puff Plus cool mint (c,d), and Puff
Bar cucumber (e,f). In the cell growth experiments (a,c,e), the x-axis shows the duration of the experiment. The y-axis shows the mean of the percent increase in cell area
(growth) over 48 h as determined using CL-Quant software. For cell
morphology data (b,d,f), the x-axis shows the treatment
concentration and the y-axis shows 24 h time intervals.
Each point is the mean of at least three experiments ± the SEM.
* = p < 0.05; ** = p < 0.01;
*** = p < 0.001; **** = p <
0.0001.
Effects
of synthetic coolants and Puff EC fluids on cell growth
and morphology in the live-cell imaging assay. Time-lapse imaging
was performed with WS-23 (a,b), Puff Plus cool mint (c,d), and Puff
Bar cucumber (e,f). In the cell growth experiments (a,c,e), the x-axis shows the duration of the experiment. The y-axis shows the mean of the percent increase in cell area
(growth) over 48 h as determined using CL-Quant software. For cell
morphology data (b,d,f), the x-axis shows the treatment
concentration and the y-axis shows 24 h time intervals.
Each point is the mean of at least three experiments ± the SEM.
* = p < 0.05; ** = p < 0.01;
*** = p < 0.001; **** = p <
0.0001.When Puff EC fluids with high levels of WS-23 (“Cool
Mint”)
and equal levels of WS-23 and WS-3 (“Cucumber”) were
tested, varying effects were observed. The effects of the “Cool
Mint” fluid (WS-23 = 45 mg/mL) and “Cucumber”
fluid (equal concentrations of WS-3 and WS-23 = 5.1 mg/mL) were evaluated
in a live-cell imaging assay. Cell growth was significantly affected
starting at about 12 h for both treatments at concentrations of >1%
(Figure c–f).
BEAS-2B cells exposed to various concentrations of Puff Plus “Cool
Mint” (Figure d) revealed elongated morphologies at 1%, rounded at 3%, or appeared
fixed at 10% starting at the first time point and extending throughout
the experiment. The morphologies observed with Puff Bar “Cucumber”
fluid (Figure f) were
either stressed and elongated (1%), rounded (3%), or fragmented (10%).
Micrographs showing segmented images taken at 0, 24, and 48 h are
presented in Figure S3b,c.
Transfer Efficiency of Aerosolized Synthetic Coolants
Refill fluids made in-house using 80% PG, water, and authentic standards
of each synthetic coolant were analyzed using GC/MS to identify and
quantify chemicals in the fluids and corresponding aerosols (Figure ). Generally, the
transfer efficiency of aerosols produced with the Baton V2 pod device
was high (Figure a).
The mean of two experiments revealed that WS-23 transferred to an
aerosol with 70% efficiency, while WS-3 transferred with 90% efficiency
(Figure b). Puff Bar
is also a low powered EC and likely has similar transfer efficiencies.
Transfer efficiency can vary with many factors, including power, and
may be higher in second- and third-generation ECs.
Figure 5
Synthetic coolants in
lab-made refill fluids and their corresponding
aerosols. (a) Concentrations of WS-23 and WS-3 in unvaped fluids,
vaped fluids, and aerosols. (b) Transfer efficiency of WS-23 and WS-3
to aerosols. Aerosols were made using a fourth-generation Baton V2
open pod EC operating at 3.7 V/8.6 W. Each bar is a mean of two measurements.
Synthetic coolants in
lab-made refill fluids and their corresponding
aerosols. (a) Concentrations of WS-23 and WS-3 in unvaped fluids,
vaped fluids, and aerosols. (b) Transfer efficiency of WS-23 and WS-3
to aerosols. Aerosols were made using a fourth-generation Baton V2
open pod EC operating at 3.7 V/8.6 W. Each bar is a mean of two measurements.
MOE Evaluation for Synthetic Coolants
The MOE, which
aids risk assessors in prioritizing the potential exposure risk to
food additives,[44,45] was used to evaluate the potential
risk from daily exposure to WS-3 and WS-23. The MOE approach considers
a reference point (e.g., the NOAEL, no observed adverse effect level)
from experimental data, an estimated daily exposure dose to the chemical
or additive, and an average adult body weight of 60 kg. The daily
consumption range of 0.5 mL (less than half the fluid in a Puff Bar
device) to 15 mL, a high daily consumption for free-base nicotine
EC fluids, was used. Using NOAEL values determined from orally administered
WS-3 and WS-23 in rats, we calculated MOEs for WS-23 (NOAEL = 5 mg/kg/bw)
and WS-3 (NOAEL = 8 mg/kg/bw)[46] based on
a 100% transfer from the EC fluid mixture into the aerosol. An MOE
below the 100 threshold for a food additive is considered high risk
requiring prioritization and mitigation by regulatory agencies. MOEs
for WS-23 were <100 for all flavors except tobacco at 1 mL consumption
per day (Figure a).
For other nicotine-salt-based disposable devices and free-base nicotine
fluids, daily consumption of 3 mL/day generated MOEs <100. In contrast,
MOEs calculated for WS-3 were <100 in 5/6 products considering
a 1 mL consumption per day (Figure b). Daily consumption of 3 mL/day generated WS-3 MOEs
<100 in only 25% of the samples for other free-base nicotine fluids.
Figure 6
MOE for
synthetic coolants in EC products. (a) WS-23 and (b) WS-3.
MOEs below the threshold of 100 indicate a potential human health
risk. The blue boxes are MOEs that were above the threshold of 100.
EC products listed below the black horizontal bar indicate refill
fluids and the Zalt brand of disposable ECs. “C” in
“C. Bomb” in Figure a = cinnamon, “PP” = Puff Plus, and “PB”
= Puff Bar.
MOE for
synthetic coolants in EC products. (a) WS-23 and (b) WS-3.
MOEs below the threshold of 100 indicate a potential human health
risk. The blue boxes are MOEs that were above the threshold of 100.
EC products listed below the black horizontal bar indicate refill
fluids and the Zalt brand of disposable ECs. “C” in
“C. Bomb” in Figure a = cinnamon, “PP” = Puff Plus, and “PB”
= Puff Bar.
Discussion
Our study investigated the chemicals in
fluids from fourth-generation
disposable Puff ECs and their toxicological effects. Over 100 chemicals,
including nicotine and two synthetic coolants, were identified in
16 “ice” and “nonice” flavors. Nicotine
concentrations in Puff fluids were generally lower than those previously
reported in fourth-generation cartridge-based fluids.[27,28,47] However, nicotine concentrations
in Puff and JUUL[28] were higher than those
in free-base nicotine EC refill fluids.[48−52] Two synthetic coolants (WS-3 and WS-23), often used
in cosmetics, personal hygiene products, and edibles, were present
in Puff EC fluids at concentrations higher than recommended for consumer
products.[46] The concentrations of WS-23
that inhibited mitochondrial reductases and cell growth were well
below the concentrations in the Puff EC fluids. Concentration–response
curves for toxic effects were significantly correlated with nicotine,
ethyl maltol, and WS-23 concentrations. For most Puff ECs, the MOEs
for the synthetic coolants were below the acceptable threshold of
100 for food additives, indicating a potential health risk.Flavor chemicals in EC fluids and aerosols are frequently found
in high concentrations and often account for a significant fraction
of the total chemicals in EC products.[14,18] We have previously
categorized “dominant flavor chemicals” as those at
concentrations ≥1 mg/mL.[17] JUUL
products generally had 0–1 dominant flavor chemical/product.[28] In contrast, most (n = 13)
Puff ECs had more than one dominant flavor chemical, and nine Puff
e-cigarettes had two or more/products. Three Puff Bars (“Sour
Apple,” “Tangerine Ice,” and “Cucumber”)
did not have any dominant flavor chemicals. Puff Bar “Tobacco”
contained the highest total flavor chemical concentration, with dominant
chemicals being ethyl maltol, vanillin, corylone, and ethyl vanillin.
In contrast, JUUL “Classic” and “Virginia Tobacco”
did not have any dominant flavor chemicals,[28] similar to other previously examined tobacco-flavored refill fluids.[15] Although menthol was the dominant flavor chemical
in “minty” Puff ECs, its concentration was two times
higher in Puff Plus “Cool Mint” than in Puff Bar “Menthol”. p-Menthone, which may be added to enhance the minty flavor,
was also dominant in Puff Plus “Cool Mint” and previously
found at high levels in LiQua “Cool Menthol” refill
fluids.[15] Triacetin, a dominant flavor
chemical in Puff Bar “Menthol,” may have been added
to produce a fruity accent, or in the case of “Sour Apple,”
it may have formed in part by a reaction between acetic acid and PG.
In our prior studies, triacetin was not used frequently in American
manufactured e-fluids.[14] However, it was
the most commonly used flavor chemical in a Russian brand (Ritchy
LTD), distributed worldwide with high concentrations in fruity-flavored
fluids (13–22.5 mg/mL) and a mint-flavored product without
menthol (44.3 mg/mL).[15] Ethyl maltol, a
dominant and frequently used flavor chemical in multiple EC libraries,[15] was in almost all Puff products at >1 mg/mL.
In some previous studies, ethyl maltol was the most cytotoxic flavor
chemical in the MTT assay, and its concentration was correlated with
the cytotoxicity of JUUL and LiQua EC fluids.[15,18,28]Some of the dominant flavor chemicals
in Puff and JUUL ECs frequently
appeared in high concentrations in our prior studies (e.g., menthol,
ethyl maltol, benzyl alcohol, vanillin, and triacetin).[13,15,17] Ethyl acetate and 3Z-3-hexen-1-ol were found in most Puff products, generally at concentrations
<1 mg/mL. Ethyl acetate, which has low cytotoxicity in the MTT
assay, was also present in most products in popular refill fluids.[18]Both JUUL and Puff EC fluids contained
benzoic acid, and two Puff
flavors (“Sour Apple” and “Aloe Grape”)
also had acetic acid. In addition, both 2-hydroxypropyl acetate and
1,2-propanediol-2-acetate were major nontarget chemicals in “Sour
Apple,” “Aloe Grape,” “Tangerine Ice,”
and “Peach Ice.” Both compounds are acetates of PG,
which may be added as solvents or fruit flavorants, or form as reaction
products between PG and acetic acid. Since acetic acid was a major
nontarget chemical, it may be a reaction product.Synthetic
coolants were rarely used in earlier generations of EC
products. When present, their concentrations were about 0.2 mg/mL
in cartomizer fluids and 0.1–3.9 mg/mL in refill fluids, with
WS-23 generally being higher than WS-3 (Table S1). WS-3 and WS-23 concentrations in Puff ECs sold in the
USA were greater than those in JUUL pods sold in Europe or the USA.[19,53] The synthetic coolants were present in all Puff ECs, while only
two of eight JUUL flavors had synthetic coolants, which were significantly
lower in concentration. WS-3 and WS-23 do not add flavor but impart
a cooling sensation and were found in “ice” and “nonice”
fruit, berries, and tobacco flavored Puff EC flavors. Concentrations
of chemicals recently reported generally agreed with our data, except
for menthol in “Cool Mint,” which was 22 times higher
in our samples.[54] This observation suggests
batch-to-batch variations in Puff products. The constituents of EC
fluids are rapidly evolving. In 2018, JUUL products contained very
high nicotine concentrations combined with benzoic acid, which was
not the case with refill fluids before the introduction of JUUL. Some
Puff ECs contain synthetic coolant concentrations that are ∼450
times higher than the concentrations in JUUL (45.1 mg/mL in Puff Plus
“Cool Mint” vs 0.1 mg/mL in JUUL “Classic Menthol”).[19] The concentrations of nicotine, synthetic coolants,
and flavor chemicals in Puff ECs are concerning and demonstrate the
need for more attention to evolving EC constituents.Fourth-generation
JUUL pods are characterized by high concentrations
of nicotine (∼61 mg/mL).[28] Likewise,
nicotine was relatively high in concentration in Puff products (40.6–52.4
mg/mL). In a related study, nicotine in Puff ECs ranged from 29.4
to 40.7 mg/mL,[52] while another study found
83.4 mg/mL.[55] Differences in reported concentrations
for Puff ECs may be due to the methods used to quantify nicotine or
variations in manufacturing different batches. In both studies, the
reported nicotine concentrations are high relative to earlier generation
products. PG/G ratios are similar to those reported previously for
Puff products.[55]Chemicals in EC
products impair cell processes and induce inflammatory
responses in multiple cell types.[16−23] The concentrations of flavor chemicals and synthetic coolants in
EC products are high enough to affect cell growth and morphology during
acute exposure. In the current study, the cytotoxicity of Puff EC
fluids in the MTT and NRU assays was significantly correlated with
total chemical concentration and individual chemicals (nicotine, WS-3,
WS-23, and ethyl maltol). The IC50s of fluids were lower
when compared to similar flavors from JUUL in the MTT and NRU assays.[28] We previously showed that the IC50 is reached for nicotine at 0.9 mg/mL in the MTT assay.[18] The nicotine concentrations in Puff ECs are
high enough to contribute to the toxicity of the fluids at the medium
to high concentrations tested in the current study. Ethyl maltol,
a frequently used dominant chemical,[15] impairs
the activity of mitochondrial reductases in BEAS-2B and mouse neural
stem cells, with IC50s of 0.06 and 0.03 mg/mL in the MTT
assay, respectively. The concentrations of ethyl maltol in Puff EC
fluids are well above the IC50s reported previously.[18] Both synthetic coolants in Puff ECs were evaluated
for cytotoxicity, and WS-23 had a significant effect on mitochondrial
metabolism at concentrations 90 times lower than those in Puff EC
fluids (IC50 = 1 mg/mL). Our live-cell imaging analysis
shows that WS-23 significantly affected cell growth and morphology
shortly after the onset of treatment.There are conflicting
reports on websites regarding the solubility
of WS-23. PubChem and the Food and Agriculture Organization (FAO)
of the United Nations report it is insoluble in water.[56,57] The Good Scents Company and ChemHub websites report its solubility
to be 0.45 mg/mL in water.[58,59] In contrast, European
and Chinese websites[60−62] have reported the solubility of WS-23 to be ∼7
mg/mL, which is higher than the highest concentration we tested (4.5
mg/mL). To verify that WS-23 was dissolved at 4.5 mg/mL in our experiments,
we tested its solubility in water and BEAS-2B culture medium at various
concentrations (Figure ). At 4.5 mg/mL, WS-23 was completely dissolved in water and culture
medium (Figure c–f).
At 7 mg/mL, WS-23 was soluble in water but not in culture medium (Figure g,h). At 9 mg/mL,
a concentration above all reported solubilities, the chemical was
partially soluble in water and insoluble in culture medium (Figure i,j). These data
show that WS-23 was completely dissolved in our experiments at the
highest concentration tested and further show that its reported solubility
is incorrect on some websites.
Figure 7
Stereoscopic microscopy images of droplets
of water or culture
medium containing various concentrations of WS-23 to show solubility
(a–j). Both 0.45 and 4.5 mg/mL of WS-23 were soluble in water
and culture medium (c–f). WS-23 (7 mg/mL) was soluble in 1
mL of water but not in BEAS-2B medium (g,h). Precipitates were present
in both water (red arrows) and the culture medium containing 9 mg/mL
(i,j). Blue arrows show air bubbles within the glass beads. The highest
concentration used in our study was 4.5 mg/mL. The solubility of WS-3
and its toxicity at the reported 0.02 mg/mL concentration is shown
in Figure S4.
Stereoscopic microscopy images of droplets
of water or culture
medium containing various concentrations of WS-23 to show solubility
(a–j). Both 0.45 and 4.5 mg/mL of WS-23 were soluble in water
and culture medium (c–f). WS-23 (7 mg/mL) was soluble in 1
mL of water but not in BEAS-2B medium (g,h). Precipitates were present
in both water (red arrows) and the culture medium containing 9 mg/mL
(i,j). Blue arrows show air bubbles within the glass beads. The highest
concentration used in our study was 4.5 mg/mL. The solubility of WS-3
and its toxicity at the reported 0.02 mg/mL concentration is shown
in Figure S4.Menthol and structurally related synthetic coolants
such as WS-3
activate the TRPM8 channels located on cells, allowing ion influx
and creating a cooling sensation, followed by activation of downstream
inflammatory responses.[38] WS-23 differs
structurally from menthol yet imparts a cooling sensation. However,
the lower potency of WS-23 to activate TRPM8 channels compared to
menthol[63−65] may indicate that other targets, including promiscuous
TRP channels outside the M8 subfamily, may be involved in its effects
on cells. Since these synthetic coolants, such as flavor chemicals,
were not originally intended for use in inhalable products, minimal
data exist on their adverse effect in humans after inhalation. A recent
rat inhalation study found no significant effects of WS-23 on body
weight, food consumption, and relative organ weights after a 4 h acute
exposure and a 14 day observation period.[66] In the same study, a 28 day subacute exposure followed by 28 days
of recovery found no significant differences in body weight, food
consumption, blood parameters, serum biochemistry, urine, pulmonary
function, organ weight, and bronchoalveolar lavage fluid.[66] However, the high dose used in the rat study
(342.85 mg/m3) was one-eighth the concentration (2813 mg/m3) calculated for air exposure based on the highest concentration
of WS-23 (45.1 mg/mL) in our study (assuming a 40 mL puff, 2.5 mg/puff,
an aerosol density of 1 g/mL and WS-23 concentration). The concentration
in the rat study may not have been sufficient to produce an effect,
and/or the chosen endpoints may not have been affected. Similar animal
exposure experiments using higher doses would be helpful.Flavor
chemicals are used in EC products at levels that exceed
concentrations in other consumer products.[15,19] Although these flavor chemicals are designated “Generally
Regarded As Safe” (GRAS) for ingestion, the Flavor Extract
Manufacturers Association (FEMA) does not endorse their use for inhalation.[67] The concentrations of dominant flavor chemicals
in Puff fluids were generally higher than those in edible products,
except for ethyl vanillin in imitation vanilla extracts, which are
diluted before use (Tables S4 and S5).[68−72] Ethyl maltol, which imparts a sweet flavor, is frequently used at
high concentrations in EC products.[13,14,17,19] In edibles (e.g., beverages,
candy, chewing gum, ice cream, and baked goods) and cosmetics (e.g.,
soaps, detergent, lotions, and perfume products), it is recommended
that ethyl maltol concentrations do not exceed 0.4%.[68−73] However, ethyl maltol in Puff fluids ranged from 0.007 to 0.99%
and exceeded ingestible concentrations in 77% of the products when
present. Ethyl maltol and some other flavor chemicals (e.g., ethyl
vanillin and γ-decalactone) increase free radical formation
in EC aerosols[74] and contribute to the
toxicity of EC fluids.[15,17,18]Like flavor chemicals, synthetic coolants are designated GRAS
and
used in edible and skincare products.[71,72] Even though
their safety designation does not apply to inhalation, they have been
used in tobacco products at 263–2300 ng/stick[75] concentrations. The evolution of EC products has seen increased
levels of synthetic coolants, especially with fourth-generation disposable
products. WS-23 is used at 0.0008–0.3% in beverages, hard candy,
confectionaries, and chewing gums.[71] However,
in Puff ECs, concentrations ranged from 0.08 to 4.51%. WS-3, another
popular synthetic coolant, was found in fewer Puff ECs (38%) at 0.14–1.64%
concentrations, exceeding maximum levels regarded as safe in beverages,
ice creams, confectioneries, candy, and chewing gum (range = 0.001–0.12%).[72] In the current study, the concentrations of
synthetic coolants were up to thousands of times higher than in edible
products and toxic in in vitro assays at concentrations lower than
those found in Puff fluids.[18] Consumers
may be unwittingly exposed to high levels of synthetic coolants in
“nonice” Puff ECs. Long-term studies with humans will
be needed to fully understand the health effects of chronic inhalation
of high concentrations of synthetic coolants.Risk assessors
use the MOE to evaluate carcinogenic risk or chemical
safety based on predicted or estimated exposure levels. Since minimal
data exist for inhalation exposures and toxicity, parameters based
on oral administration of a chemical in experimental animals are often
used.[76] Nongenotoxic and noncarcinogenic
chemical substances with MOEs less than 100 are generally considered
a health risk. The concentrations of synthetic coolants in inhaled
tobacco products exceed those in edible products. Calculated MOEs
for WS-3 and WS-23 are well below 100 for almost all Puff products
at 1 mL of fluid/day, thereby presenting a safety risk to consumers.
Mint and “ice” flavored Puff ECs had the lowest MOEs,
consistent with higher concentrations of synthetic coolants. Puff
products that contained both synthetic coolants at levels that generated
MOEs below the 100 thresholds would increase the exposure risks to
users. Because the oral and inhalation toxicities are not always equivalent,
route-to-route extrapolations routinely used by regulatory agencies[77,78] may be required for a more realistic exposure model in humans. Considering
the increased sensitivity of the respiratory tract to toxicants, the
MOE values calculated for Puff ECs underestimate exposure.[77,78] The Joint FAO/WHO (Food and Agricultural Organization of the United
Nations/World Health Organization) Expert Committee on Food Additives
concluded that further research is needed to assess the risk of synthetic
coolants to humans.[76]Future work
should evaluate the use and concentrations of synthetic
coolants in new EC products as they evolve. It would also be informative
to examine exposure at the air-liquid interface using aerosolized
synthetic coolants.In summary, our data show that the fluid
composition of ECs is
evolving, with the most recent major change being the inclusion of
high concentrations of synthetic coolants, which were toxic in our
in vitro assays. The ban on flavored cartridge-based EC products caused
a migration of adolescents and young adults from cartridge-based products
such as JUUL to disposable ECs such as Puff, which is exempt from
the flavor ban. These new disposable ECs, exemplified by the Puff
brand studied here, have much higher concentrations of synthetic coolants
than those found in JUUL. The high levels of nicotine, flavor chemicals,
and synthetic coolants, which exceeded those used in other consumer
products, raise a concern about the safety of Puff products. Product
manufacturers are increasing the youth-attracting synthetic coolant
content of ECs, while the inhalation risks remain unknown. This practice,
in effect, represents a large, uncontrolled experiment in the lungs
of youth and other consumers and highlights the need for regulation
to protect public health.
Authors: Peyton A Tierney; Clarissa D Karpinski; Jessica E Brown; Wentai Luo; James F Pankow Journal: Tob Control Date: 2015-04-15 Impact factor: 7.552
Authors: Joseph H Lucas; Thivanka Muthumalage; Qixin Wang; Michelle R Friedman; Alan E Friedman; Irfan Rahman Journal: Front Physiol Date: 2020-09-04 Impact factor: 4.566