- Research article
- Open Access
Assessment of an in vitro whole cigarette smoke exposure system: The Borgwaldt RM20S 8-syringe smoking machine
© Adamson et al 2011
Received: 6 May 2011
Accepted: 26 August 2011
Published: 26 August 2011
There have been many recent developments of in vitro cigarette smoke systems closely replicating in vivo exposures. The Borgwaldt RM20S smoking machine (RM20S) enables the serial dilution and delivery of cigarette smoke to exposure chambers for in vitro analyses. In this study we have demonstrated reliability and robustness testing of the RM20S in delivering smoke to in vitro cultures using an in-house designed whole smoke exposure chamber.
The syringe precision and accuracy of smoke dose generated by the RM20S was assessed using a methane gas standard and resulted in a repeatability error of ≤9%. Differential electrical mobility particle spectrometry (DMS) measured smoke particles generated from reference 3R4F cigarettes at points along the RM20S. 53% ± 5.9% of particles by mass reached the chamber, the remainder deposited in the syringe or connecting tubing and ~16% deposited in the chamber. Spectrofluorometric quantification of particle deposition within chambers indicated a positive correlation between smoke concentration and particle deposition. In vitro air-liquid interface (ALI) cultures (H292 lung epithelial cells), exposed to whole smoke (1:60 dilution (smoke:air, equivalent to ~5 μg/cm2)) demonstrated uniform smoke delivery within the chamber.
These results suggest this smoke exposure system is a reliable and repeatable method of generating and exposing ALI in vitro cultures to cigarette smoke. This system will enable the evaluation of future tobacco products and individual components of cigarette smoke and may be used as an alternative in vitro tool for evaluating other aerosols and gaseous mixtures such as air pollutants, inhaled pharmaceuticals and cosmetics.
Molecular mechanisms and pathways elucidating cigarette smoking disease processes are still not well understood. Abundant epidemiological studies and research have linked smoking to a number of diseases including lung cancer, chronic obstructive pulmonary disease and cardiovascular disease; identified inflammatory and oxidant stress mechanisms having a pivotal role in all of these processes . Physiologically-relevant in vitro model systems, in which human lung cells and tissues can be exposed to appropriate doses of cigarette smoke may provide useful tools to interpret these processes and identify other mechanisms. There are numerous studies reporting the development of such in vitro models utilising a variety of cell types and systems [2–8]. However, just as the selection and cultivation of these selected cells and systems are important, so too is the development, generation and delivery of cigarette smoke to these in vitro assays.
Traditionally, toxicological evaluation of cigarette smoke has focussed on the particulate fraction of smoke. The particulate matter (PM) from cigarette smoke is collected on a Cambridge filter pad  and eluted with an organic solvent such as methanol or dimethyl-sulphoxide to generate a solution [10, 11] which can be easily added to traditional submerged in vitro cultures. This fraction of cigarette smoke only contains the particulate element, which constitutes approximately 5-10% of cigarette smoke by weight. The remaining 90-95% constitutes the gas/vapour phase of smoke and is not captured on the Cambridge filter pad . Water-soluble cigarette smoke components from both particulate and vapour phases can be captured by bubbling cigarette smoke through biological buffers or tissue culture media. This resulting 'aqueous extract' can also be easily assessed in submerged in vitro cultures [13–15]. However, in order to understand the toxicological and biological effect of cigarette smoke, the whole cigarette smoke, i.e., both particulate and vapour phase, needs to be analysed.
In conjunction with Borgwaldt, we have expanded the capability of the smoke delivery system with the addition of another four syringe unit. This addition has resulted in a new expanded eight syringe system, requiring characterisation which has not been conducted previously. Adapting the system from four to eight syringes increases the number of available whole smoke doses per run and reduces the number of experimental runs (eliminating the need for back-to-back runs) which results in a single biological dose response to be carried out in one experimental run. This adaptation will enhance the RM20S by increasing flexibility in experimental design, by reducing inter-run variability and by saving time.
The aim of this study was to characterise and evaluate the performance of the expanded RM20S eight syringe smoking machine and to assess cigarette smoke through the system. Initially all syringes were calibrated for precision and accuracy. Using a hydrocarbon analyser and test gas the syringes could be tested to confirm to what extent, collectively and individually, smoke was being delivered at its target dilution. The penetration and deposition of cigarette smoke particulate throughout the RM20S whole smoke exposure system was investigated using two dosimetry techniques. The first employed the use of differential electrical mobility particle spectrometry (DMS) to enable in-line and real-time particle diameter and concentration measurement of smoke along the whole smoke system . It had been previously reported by Scian et al., (2009) that the Burghart Mimic Smoker-01® system has smoke losses of up to 50% preceding delivery to cells . Data generated from the DMS would enable us to calculate smoke losses experienced in our exposure system and compare them to this recent study. The second technique used spectrofluorometric analysis to quantify particulate deposition on inserts within the exposure chamber during whole smoke exposures. Particulate is extracted followed by absorbance measurements which can be converted into concentrations using a PM standard curve. Finally, to confirm previous non-cell based methods  using cell cytotoxicity, positional exposure chamber dosimetry was examined to ensure the same dose of cigarette smoke was being delivered to each insert within a single chamber. H292 lung epithelial cells were cultured on individual inserts within an exposure chamber, exposed to whole smoke and cytotoxicity assessed using the Neutral Red Uptake (NRU) assay.
Results from this study have given us further confidence that the current whole smoke exposure system, using the Borgwaldt RM20S smoking machine and the BAT exposure chamber, is a reliable, repeatable, robust and potentially a more physiologically relevant method of generating and exposing in vitro cellular and tissue cultures to whole cigarette smoke at the ALI. We propose to further characterise whole smoke dosimetry relative to specific smoke constituents and to use this system for the evaluation of novel cigarette design modifications proposed to reduce toxicants in smoke and to further investigate individual components of cigarette smoke.
Syringe validation using hydrocarbon analysis
Initially, before conducting any in vitro whole smoke exposures with the RM20S, all eight syringes were calibrated for precision and accuracy using a methane standard gas. Using a hydrocarbon analyser and methane test gas at two dilutions (1:193 and 1:500 (test gas:air, volume:volume)), the syringes, individually and collectively, were assessed to determine if they were achieving the target deliveries of 520 ± 20 ppm and 200 ± 15 ppm methane gas standard respectively.
At a dilution of 1:500, individual syringe precision indicated a 15% positive bias of average syringe outputs about the target (200 ± 15 ppm) (Figure 3B). Dunnet's test showed that collectively the syringes were significantly different from the target. Repeatability, as a percentage of the nominal values, was 5% and the Gage R&R estimate as a percentage of the nominal values was 8.9%. Although bias was significant, it only accounts for the overall position of the data and not the precision of syringe delivery, therefore bias can be significant yet the R&R estimate be fit for purpose within the same scenario. All of these values were < 10%, and hence deemed to be fit for purpose despite significant bias.
A two-way ANOVA was conducted to assess the syringe outputs across both dilutions and overall accuracy. At the dilutions measured there was no significant difference in the syringes (p = 0.051). Total Gage R&R was 2.9%, reproducibility was 2.2% and repeatability was 1.9% for the entire syringe system at both dilutions tested. These results show that collectively the syringe system is fit for purpose.
Smoke transfer efficiency using an electrical mobility spectrometer
Particle penetration was calculated by both particle mass and number, by comparing the total smoke particulate at three points. The values were reported relative to 100% smoke mass equivalent to 5.75 ± 0.31 mg (assuming unit density), and 100% smoke particle number equivalent to 1.44 × 1012 ± 0.10 × 1012 particles (n = 3) for 10 puffs from 2 cigarettes (6+4) as measured by the DMS-smoke cycle simulator (SCS) system pre-dilution at the point of generation. This matches the 10 puff data collection at the other sample points. Data was corrected for the theoretical delivered fraction at each sampling point as calculated based on the dilution settings and mechanism. Pre-chamber losses were calculated by the difference in smoke concentration between the point of smoke generation (100%) and the chamber (β), and chamber deposition was calculated by the difference in smoke concentration before (β) and after (γ) the chamber.
Summary of the assessment of total cigarette smoke particulate sampled at the exit of the syringe (α), before the chamber (β) and at the exit from the chamber (γ) using an electrical mobility spectrometer; existing polyurethane was the tubing installed.
Particle mass penetration (%)
Particle number penetration (%)
Count Median Diameter (nm)
Volume Median Diameter (nm)
Pairwise comparison using the General Linear Model showed that there were statistically significant differences (p = < 0.05) between all three sampling points in terms of particle number, particle mass and VMD. However, for CMD there was only a significant difference between the α and γ sampling points; for CMD there was little difference between α and β (p = 0.0549), and between β and γ (0.7384).
Deposition assessment using fluorometric analysis
The linear range of the graph was over 2 orders of magnitude for smoke dilution (1:5 - 1:400 (smoke:air, v/v)) with particle mass deliveries of 60.74 - 0.63 μg/cm2. The Limit of Quantification (LOQ) and Limit of Detection (LOD) were calculated to be 0.448 and 0.247 μg/cm2 respectively. The R-square value for the linear regression was 0.916. As expected, the data showed that there was a positive correlation between smoke concentration and particulate depositing on the inserts.
Summary of calculated 3R4F particulate deposition on inserts within the exposure chamber (μg/cm2).
Equivalent 3R4F particulate deposition (μg/cm2)
60.74 ± 2.07
29.47 ± 1.30
11.33 ± 0.59
5.50 ± 0.58
2.67 ± 0.13
1.03 ± 0.11
0.63 ± 0.09
Exposure chamber dosimetry
In this study we present a characterised and evaluated system used to generate, dilute, deliver and expose in vitro cell cultures to whole smoke at the ALI. The integrity of whole smoke generated and delivered to in vitro cultures was assessed using a measurement systems analysis approach. We characterised three key areas within the exposure system; delivery and accuracy of dilution syringes, smoke particle penetration and smoke losses through the system, and positional deposition in the exposure chamber.
Individual syringe precision and accuracy were measured using the hydrocarbon analysis method described. The syringes were tested at two dilutions, 1:500 and 1:193 (a calibration standard dilution), as this represents the extreme top and mid dilutions respectively used in the laboratory to generate a biological dose response range using robust in vitro primary and continuous cell cultures [7, 17]. We observed more variation about the higher dilution of 1:500, target value of 200 ppm methane gas, when compared to the lower dilution of 1:193, target value of 520 ppm methane gas; this was primarily because the syringe sensors were adjusted at the latter dilution. At a dilution of 1:500 there was a positive bias about the target of 15%, suggesting at this dilution, collectively the syringes were delivering 15% more gas, and could therefore deliver 15% more smoke. This is something which cannot currently be improved upon, as bias fluctuates at different dilutions tested, but this can be adjusted for with further syringe calibration.
Furthermore, earlier evaluations from data taken at four dilution levels (1:1000, 1:500, 1:250, 1:193) demonstrated that both repeatability and the Gage R&R estimate improved as the dilution was decreased (smoke concentration increased) towards the biological dose response range previously described (data not shown). This may be due to the reduction in serial dilutions the syringe has to make as smoke concentration increases, and therefore eliminating additional stages of potential error. At a dilution of 1:193 there was no bias of syringe delivery about the target and the Gage R&R estimate was 3%. Statistical analysis indicated no significant differences in the syringes and Total Gage R&R to be within acceptable limits (< 10%). These results have demonstrated that within the biological dose response range, individual syringe precision and accuracy of whole smoke dilutions are fit for purpose which suggests confidence in the programmed dilution of smoke generated by the RM20S. This study is further supported by a previous RM20S inter-laboratory study by Kaur et al., (2010) comparing syringe validation using CH4 measurements; in two different laboratories and with two different operators there was comparable reproducibility and precision for commonly used whole smoke dilutions .
For whole smoke exposure systems in general, it is important to understand smoke losses and smoke changes between the point of generation and exposure chamber and smoke deposition within the chamber itself. Looking only at the existing polyurethane (preferred tubing), average particle penetration to the chamber was 53% by mass, implying that there are losses (about 47%) within the syringe or within the tubing between the syringe and the chamber. This is also consistent with the Burghart Mimic Smoker-01® system which reported smoke losses of up to 50% preceding delivery to cells . Repeat studies indicated smoke penetration was very consistent in the RM20S, so smoke delivered to the chamber will be consistent at this dilution setting of 1:60 (smoke:air, v/v).
Particle penetration by number to each of the sampling points was significantly less than particle mass. It is the loss of particle number prior to α that is important; this is assumed to be caused by significant pre-dilution coagulation of particles resulting in reduced particle number (14% reduction in number). The percentage particle loss by number and mass between sample point α and sample point β was relatively consistent; 30% number and 40% by mass lost (relative). Additionally the VMD at sample point β (393.8 nm) was less than at sample point α (422.9 nm). These imply that larger particles are preferentially being lost in the syringe/tubing. Therefore it is likely that most of the observed losses occurred in the syringe during the generation of serial dilutions of smoke and turbulent airflow, and there is evidence for this in the rapid visual build-up of tar on the glass surface during frequent usage.
Furthermore we investigated the use of other tubing types in the RM20S system: existing polyurethane (used tubing, currently installed in the RM20S and having a visible build up/conditioning of tar), unused polyurethane and unused Viton®, a PTFE-like non-stick fluoroelastomer. Identical DMS dosimetry studies using different tubing types, including the Viton®, suggest that the choice of tube material did not matter for these three.
To complement the DMS dosimetry studies, we have also assessed particulate deposition using high performance liquid chromatography. Particulate, generated from different whole smoke doses from reference 3R4F cigarettes (10 mg tar), captured on blank inserts were collected, eluted, and quantified in μg/cm2 using a PM standard curve. A reference table was generated from the data obtained to allow comparisons between particulate deposition and whole smoke dilution. We have conducted similar studies using other cigarette types with different tar deliveries (6 mg and 1 mg ISO pack tar compared with 3R4F 10 mg ISO pack tar). Data indicated there was a clear difference in particulate depositing on the inserts from each of the different cigarette types, with a greater amount of particulate depositing from the highest delivery 10 mg 3R4F product, followed by the 6 mg product which in turn is greater than the 1 mg product. For example, at a 1:5 smoke dilution (smoke:air, v/v) generated by the RM20S, particulate delivery was 61.05 ± 2.07, 38.11 ± 2.21 and 3.09 ± 0.21 μg/cm2 for the 10, 6 and 1 mg products respectively.
Finally, exposure chamber dosimetry was assessed by measuring cell viability within a single chamber, and comparing cell inserts which were exposed to the same dilution of cigarette smoke. Previous studies on the Borgwaldt RM20S and exposure chamber using chemical analysis techniques reported particulate deposition in the chamber to be uniform  however this had never been tested before using a biological endpoint. Cell viability assessed using the NRU assay was used as a quick and robust method to test for differences in doses between cell inserts. As verified by a p-value of 0.56, there was no significant difference in cell viability at the dose tested within a single chamber, demonstrating that smoke/cell monolayer interactions were equal across all inserts within a chamber (mean viability 46 ± 9.8%).
Materials and methods
Cell culture and whole smoke exposure
Human pulmonary carcinoma cells (NCI-H292) from the American Type Culture Collection (ATCC; passages 90-94) were cultured in complete RPMI cell culture medium and incubated at 37°C, 5% CO2. Cells were seeded in 12 mm diameter, 0.4 μm pore size inserts (Transwell®, Corning, Schiphol-Rijk, The Netherlands) 2 days prior to exposure, at a density of 3 × 105 cells/ml. Cells were exposed to mainstream cigarette smoke at the air-liquid interface, using the BAT exposure chamber as previously described (Figure 1) [7, 17]. In brief, six inserts were placed in a single exposure chamber and exposed to cigarette smoke for 30 minutes at a dilution of 1:60 (smoke:air, v/v); this is approximately the half maximal effective concentration (EC50) of 3R4F cigarette whole smoke to induce 50% cytotoxicity in exposed H292 cells, as determined by previous experiments .
Air and incubator controls were also included in each run. Air control cells were exposed to a continuous flow of sterile air in an exposure chamber, at 200 cm3/min for a 30 minute duration, at the same time as whole smoke exposed cells. Incubator control cells remained in submerged condition in cell culture incubators throughout the exposures.
Cigarette smoke generation
3R4F reference cigarettes (10 mg ISO pack tar) (University of Kentucky, Kentucky, USA) were smoked at a programmed dilution of 1:60 (smoke:air, v/v) according to ISO 4387:1991  (35 ml puff over 2 seconds, once a minute), as previously described . Between puffs, smoke was allowed to remain in the exposure chamber and was only expelled passively when the next puff replaced it. Allowing smoke to age during the deposition phase of the cycle in this exposure system differs from alternative flow-through systems for smoke exposure reported elsewhere [20–22]. The rationale in this case was to increase relative deposition efficiency and improve precision of deposition by allowing diffusion and sedimentation from still air in a symmetrical exposure chamber. The 3R4F cigarettes were conditioned for a minimum of 72 hours prior to smoking (60 ± 3% relative humidity, 22 ± 1°C) according to ISO 3402:1999 . Prior to smoking, three quality checks were performed on the RM20S as follows: the air velocity was verified to be 20 ± 3 cm3/sec; checks were performed for air leaks (acceptable range of pressure between 2750 and 3000 Pa); and the puff volumes were adjusted on each syringe to 35 ± 0.3 ml .
Syringe validation using hydrocarbon analysis
To assess syringe accuracy and precision within the Borgwaldt RM20S, a total hydrocarbon analyzer - 3010P MINIFID Portable Heated Flame Ionisation Detection (FID) (Signal Group Ltd, Surrey, UK) was used to measure syringe output, as recommended by Borgwaldt. This FID has a stated accuracy of better than ± 0.2 ppm, with linearity better than ± 0.05 ppm for an analyte range of 0-100,000 ppm hydrocarbon, so was therefore well suited for this study as the measured CH4 concentrations ranged between 100-520 ppm . A 10% (± 0.5%) methane/nitrogen (CH4/N2) test gas (Air Products PLC, Cheshire, UK) was diluted by all 8 syringes simultaneously, in the same way they would dilute cigarette smoke.
Each syringe output line was attached to a separate, vacuumed, 1.5 litre gas collection bag. After 9 minutes of syringe dilution and methane test gas collection (the length of time taken to fill a single bag) all bags were detached and the contents read using the hydrocarbon analyser. The analyser ignition fuel used was a mixture of hydrogen and helium gases (40% H2, 60% He) (Air Products PLC, Cheshire, UK). The analyser calibration gas was 500 parts per million (ppm) methane/air (CryoService Ltd, Worcester, UK).
The contents of each bag were recorded as ppm of the total methane test gas collected, and these were compared to a target ppm value for the dilutions used. Two dilutions were tested alternately to reduce mechanical bias, 1:500 and 1:193 (gas:air, v/v); n = 15 was the data set for each. The dilutions of 1:500 and 1:193 (a calibration standard dilution) were selected as this represents a low and mid dose of smoke respectively in the H292 cell line biological dose response range; the typical range being 1:1000 - 1:20 . Methane target values for 1:500 and 1:193 were 200 ppm and 520 ppm respectively. Between alternate dilutions, gas collection bags were vacuumed with a pump and a clearing puff was initiated on the RM20S to clear all syringes and tubing of residual gas.
Smoke transfer efficiency using an electrical mobility spectrometer
To assess the extent of whole smoke loss/deposition within the tubing of the Borgwaldt RM20S smoking machine, an electrical mobility spectrometer - Differential Mobility Spectrometer 500 (DMS) (Cambustion Ltd, Cambridge, UK) was used. The DMS sampled all the smoke per puff reaching the sampling port over all 10 puffs used for assessment and recorded the average particle diameter, number and volume concentration, flow rate and time period of each sample to calculate the total number and volume of particles at different regions along the tubing.
The same single syringe of the RM20S and the same exposure chamber were used in combination for all readings to reduce inter-syringe variability and syringe-chamber pairing bias. Samples for aerosol analysis were taken at three points along its length: (α) the syringe exhaust line; (β) pre-exposure chamber and (γ) post-exposure chamber (Figure 4). Readings at these three key points along the tubing were used to quantify, qualify and calculate smoke losses within the system.
The amount of smoke at the point of generation could not be measured directly in the RM20S smoking machine as there was no suitable access point - the earliest accessible point was α, the exhaust port of the first syringe between four and six seconds after puff initiation. Measurement at the generation point was estimated by smoking the same cigarettes (3R4F) and measuring using the same DMS electrical mobility spectrometer. In this case a smoking cycle simulator (SCS) (Cambustion Ltd, Cambridge, UK) was used as the smoking engine at the ISO regime allowing direct sampling over zero to two seconds from puff initiation via a constant flow sampling system . These primary data were used to calculate subsequent smoke losses within the system.
The DMS was set to a secondary dilution of 1:60 to take α readings, as the smoke from the syringe at this stage was concentrated, but no secondary dilution for the β and γ readings was required. For γ readings the chamber was filled with 30 ml Dulbecco's Modified Eagles Medium (DMEM) (Fisher Scientific UK Ltd, Loughborough, UK) to mimic usual exposure conditions and to give the correct internal volume and humidity; media-in and media-out ports were blocked. A tap was also inserted between the DMS line and the chamber for the γ readings, and was only opened for 8 seconds to sample aged smoke when the syringe was exhausting fresh smoke into the chamber; this stopped the DMS pump continually pulling smoke from the syringe line through the chamber and causing a vacuum. This is representative of whole smoke exposures to in vitro cultures in our laboratories using the RM20S.
A three-way comparison of different types of tubing was conducted on the RM20S to assess their individual performance and to see if there was a significant reduction in smoke loss using one type of tubing over another. The three tubing types compared were: existing polyurethane (the current used tubing installed in the RM20S upon manufacture, and having a visible build up/conditioning of tar), unused polyurethane (Farnell, Leeds, UK) and unused Viton® (Altec Products Ltd, Cornwall, UK), a PTFE-like fluoroelastomer. The tubing type order and the order in which the position was read along the tubing was fully randomised and repeated three times. The length of tubing used for each smoke run was 3.4 m irrespective of tubing type. For unused Viton® and unused polyurethane, new lengths of tubing were installed for each repeat experiment; when conditioned polyurethane was removed for another type of tubing, it was retained and later reinstalled for repeat experiments.
Deposition assessment using fluorometric analysis
Particle deposition within the whole smoke exposure chamber was determined by exposing inserts without cells to 3R4F reference cigarette smoke at a range of dilutions, minimum of n = 4 per dilution. Before smoke exposure, blank inserts were pre-wetted with deionised water and placed into the chambers. Whole smoke was generated and delivered as previously described. Deposited particulate material was extracted from inserts using 2 ml of high performance liquid chromatography (HPLC) grade methanol (Hayman Ltd, Essex, UK) with agitation on a plate shaker set to ~150 rpm for 10 minutes. This procedure was repeated using a blank/untreated insert as a control.
Extracts were analysed by HPLC using an Agilent 1100 Series (Agilent, UK). Elution was performed isocratically with a methanol flow rate of 1 ml/minute and a sample injection volume of between 3-10 μl. Fluorescence was detected with an Agilent standard FLD cell (Agilent, UK) at excitation and emission wavelengths of 286 nm and 350 nm respectively. Particulate concentrations of the insert extracts were calculated from the standard calibration curves and the blank insert results subsequently subtracted from the extract values. ChemStation Rev.A.10.02 (Agilent, UK) software was used to undertake instrument control and quantification. Sample extracts were quantified against an external standard prepared from 3R4F generated PM . The standard calibration curve was prepared from PM concentrations ranging from 0.48 - 38 μg/ml.
Neutral Red Uptake
After whole smoke exposure, cells were transferred to complete Ultraculture (Lonza Biologics Plc, Tewkesbury, UK) containing 2 mM glutamine, 50 U/ml penicillin and 50 μg/ml streptomycin (Invitrogen, Paisley, UK) and incubated at 37°C, 5% CO2 for a 24 hour recovery period. After incubation, the Neutral Red Uptake (NRU) assay was performed to assess cell viability in each insert as previously described, based on the National Institutes of Health .
Briefly, media was removed from each insert and replaced with 50 μg/ml Neutral Red solution (Sigma-Aldrich Company Ltd, Dorset, UK) for 3 hours, to allow for the active uptake of dye into viable cells. Inserts were washed twice in pre-warmed phosphate buffered saline (Fisher Scientific UK Ltd, Loughborough, UK) to remove any residual dye. After washing, cells were lysed with 500 μl destain (50% ethanol, 49% distilled H2O, 1% glacial acetic acid). Aliquots of 100 μl elutate were read on a Multiskan Ascent Microplate Reader (Thermo Labsystems, Waltham, MA, USA) at a wavelength of 540 nm with a reference filter of 630 nm. Neutral Red blanks were also included to remove background levels of dye absorbed by the inserts. Viability of exposed cells was calculated as a percentage of air controls.
Data were reported as a mean ± standard deviation. For syringe validation, a two-way ANOVA was used to compare the syringe outputs at the two dilutions tested, Dunnet's test was used to compare results to target and look at bias, and a Total Gage R&R test was used to assess repeatability and reproducibility of all syringes at both dilutions, data set n = 15 for both dilutions. For transfer efficiency data, a General Linear Model (with Tukey's test) was used to test for differences in sample point and tubing type, data set n = 3. A one-way ANOVA was used to assess the differences in cell viability measured during the exposure chamber dosimetry study, data set n = 20. Statistical analysis for the above investigations was conducted using MINITAB® v.15.1.30 statistical software. All residual plots for all graphs were checked to ensure the quality of the data obtained. A p-value < 0.05 was considered statistically significant. Deposition analysis using fluorescence was conducted on GraphPad Prism® v.5.02, data set was at least n = 4 for all dilutions tested and reported as a mean ± standard error of mean.
In conclusion, we present a reliable and repeatable whole smoke exposure system consisting of a Borgwaldt RM20S smoking machine and BAT's exposure chamber. We are confident this system can be used to expose in vitro ALI cultures to eight independent and simultaneous doses of whole smoke knowing that smoke delivery, dilution precision, and chamber dose are reproducible and expected. This study further supports our previous study comparing syringe validation using CH4 measurements in two different laboratories; one being in the UK, the other in Canada .
This system will enable us to investigate the effects of physiologically relevant whole cigarette smoke doses on endpoints known to be relevant to major smoking related disease, namely cancer and chronic obstructive lung disease (chronic bronchitis and emphysema). Furthermore, these results can be used to support and enable quantification and alignment of whole smoke doses with human dosimetry data; recent studies within Group Research and Development (GR&D) BAT have modelled and quantified regional tissue deposition of smoke within the different compartments of the respiratory tract .
We propose to further use this exposure system for the evaluation of future tobacco products designed to reduce the harmful effects of smoke and to investigate individual components of cigarette smoke. Furthermore, this system could be a useful alternative in vitro method for evaluating the effects of other aerosols and gaseous mixtures such as air pollutants, inhaled pharmaceuticals and cosmetics, and to examine occupational exposure scenarios.
The authors would like to thank David Thorne for developing and assisting in the initial experiments using hydrocarbon analysis; Jessica Perkins and Martin Arnold for their technical support on the deposition assessment using an electrical mobility spectrometer; Liz Pearce for the HPLC analysis; and Mark Barber at Borgwaldt KC for his engineering and mechanical expertise.
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