29 research outputs found

    A strategy for efficiently collecting aerosol condensate using silica fibers:application to carbonyl emissions from e-cigarettes

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    Analysing harmful constituents in e-cigarette aerosols typically involves adopting a methodology used for analysing tobacco smoke. Cambridge filter pads (CFP) are the basis of numerous protocols for analysing the various classes of compounds representing 93 harmful and potentially harmful constituents identified in tobacco smoke by the FDA. This paper describes a simplified method for trapping the low volatility components of e-cigarette aerosols using a single trapping procedure followed by physical extraction. The trap is a plug of amorphous silica fibres (0.75 g of 4 µm diameter) within a 10mL syringe inserted between the e-cigarette mouthpiece and the pump of the vaping machine. The method is evaluated for emissions from three generations of e-cigarette device (Kangertech CE4, EVOD and Subox Mini-C). On average the silica wool traps about 94% of the vapourised liquid mass in the three devices and higher levels of condensate is retained before reaching saturation compared with CFP. The condensate is then physically extracted from the silica wool plug using a centrifuge. Condensate is then available for use directly in multiple analytical procedures or toxicological experiments. The method is tested by comparison with published analyses of carbonyls, among the most potent toxicants and carcinogens in e-cigarette emissions. Ranges for HPLC-DAD analyses of carbonyl-DNPH derivatives in a laboratory formulation of e-liquid are formaldehyde (0.182±0.023 to 9.896±0.709 µg puff-1), acetaldehyde (0.059±0.005 to 0.791±0.073 µg puff-1) and propionaldehyde (0.008±0.0001 to 0.033±0.023 µg puff-1); other carbonyls are identified and quantified. Carbonyls concentrations are also consistent with published experiments showing marked increases in with variable power settings (10W - 50W). Compared with CFPs, e-cigarette aerosol collection by silica wool requires only one vaping session for multiple analyte groups, traps more condensate per puff, collects more condensate before saturating

    A Strategy for Efficiently Collecting Aerosol Condensate Using Silica Fibers: Application to Carbonyl Emissions from E-Cigarettes

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    Analyzing harmful constituents in e-cigarette aerosols typically involves adopting a methodology used for analyzing tobacco smoke. Cambridge filter pads (CFP) are the basis of numerous protocols for analyzing the various classes of compounds representing 93 harmful and potentially harmful constituents identified in tobacco smoke by the FDA. This paper describes a simplified method for trapping the low volatility components of e-cigarette aerosols using a single trapping procedure followed by physical extraction. The trap is a plug of amorphous silica fibers (0.75 g of 4 μm diameter) within a 10 mL syringe inserted between the e-cigarette mouthpiece and the pump of the vaping machine. The method is evaluated for emissions from three generations of e-cigarette device (Kangertech CE4, EVOD, and Subox Mini-C). On average, the silica wool traps about 94% of the vaporized liquid mass in the three devices and higher levels of condensate is retained before reaching saturation compared with CFP. The condensate is then physically extracted from the silica wool plug using a centrifuge. Condensate is then available for use directly in multiple analytical procedures or toxicological experiments. The method is tested by comparison with published analyses of carbonyls, among the most potent toxicants and carcinogens in e-cigarette emissions. Ranges for HPLC-DAD analyses of carbonyl-DNPH derivatives in a laboratory formulation of e-liquid are formaldehyde (0.182 ± 0.023 to 9.896 ± 0.709 μg puff-1), acetaldehyde (0.059 ± 0.005 to 0.791 ± 0.073 μg puff-1), and propionaldehyde (0.008 ± 0.0001 to 0.033 ± 0.023 μg puff-1); other carbonyls are identified and quantified. Carbonyl concentrations are also consistent with published experiments showing marked increases with variable power settings (10W to 50W). Compared with CFPs, e-cigarette aerosol collection by silica wool requires only one vaping session for multiple analyte groups, traps more condensate per puff, and collects more condensate before saturation

    X-ray photoelectron and infrared spectroscopies of quartz samples of contrasting toxicity

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    An exploratory XPS and FTIR investigation of the surfaces of bulk quartz powders widely used in toxicological studies (DQ12 and Min-U-Sil 5) was carried with the aim of correlating surface features with toxicity as reflected by indicators of biological response. Some patches of amorphous silica were identified as well as varying amounts of calcium but none of these features correlated with biological response. No evidence of widely-quoted surface silanol (SiOH) structures was found in this investigation and the possibility that FTIR artefacts have been previously misidentified as silanol structures is discussed

    Toxic metal concentrations in cigarettes obtained from U.S. smokers in 2009 : results from the International Tobacco Control (ITC) United States survey cohort

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    This research was funded by grants from the U.S. National Cancer Institute (R01 CA100362 and P01 CA138389), and the Canadian Institutes of Health Research (115016). Geoffrey T. Fong was supported by a Senior Investigator Award from the Ontario Institute for Cancer Research (OICR) and a Prevention Scientist Award from the Canadian Cancer Society Research Institute.Smoking-related diseases can be attributed to the inhalation of many different toxins, including heavy metals, which have a host of detrimental health effects. The current study reports the levels of arsenic (As), cadmium (Cd), chromium (Cr), nickel (Ni), and lead (Pb) in cigarettes obtained from adult smokers participating in the 2009 wave of the ITC United States Survey (N = 320). The mean As, Cd, Cr, Ni, and Pb levels were 0.17, 0.86, 2.35, 2.21, and 0.44 mu g/g, respectively. There were some differences in metal concentrations of cigarette brands produced by different manufacturers, suggesting differences in the source of tobaccos used by different companies. For Ni, there were significant pairwise differences between Philip Morris U.S. (PMUSA) and R.J. Reynolds (RJR) brands (PMUSA higher; p 0.10). Because of the variety of toxic heavy metals in cigarette tobacco, and their numerous negative health effects, metal content in cigarette tobacco should be reduced.Publisher PDFPeer reviewe

    Reducing toxic reactive carbonyl species in e-cigarette emissions:testing a harm-reduction strategy based on dicarbonyl trapping

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    Reducing the concentration of reactive carbonyl species (RCS) in e-cigarette emissions represents a major goal to control their potentially harmful effects. Here, we adopted a novel strategy of trapping carbonyls present in e-cigarette emissions by adding polyphenols in e-liquid formulations. Our work showed that the addition of gallic acid, hydroxytyrosol and epigallocatechin gallate reduced the levels of carbonyls formed in the aerosols of vaped e-cigarettes, including formaldehyde, methylglyoxal and glyoxal. Liquid chromatography mass spectrometry analysis highlighted the formation of covalent adducts between aromatic rings and dicarbonyls in both e-liquids and vaped samples, suggesting that dicarbonyls were formed in the e-liquids as degradation products of propylene glycol and glycerol before vaping. Short-term cytotoxic analysis on two lung cellular models showed that dicarbonyl-polyphenol adducts are not cytotoxic, even though carbonyl trapping did not improve cell viability. Our work sheds lights on the ability of polyphenols to trap RCS in high carbonyl e-cigarette emissions, suggesting their potential value in commercial e-liquid formulations

    Challenges in predicting the change in the cumulative exposure of new tobacco and related products based on emissions and toxicity dose–response data

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    Funding: This work was funded by the Netherlands Food and Consumer Product Safety Authority (NVWA), Utrecht, the Netherlands. Project number 9.7.1Many novel tobacco products have been developed in recent years. Although many may emit lower levels of several toxicants, their risk in the long term remains unclear. We previously published a method for the exposure assessment of mixtures that can be used to compare the changes in cumulative exposure to carcinogens among tobacco products. While further developing this method by including more carcinogens or to explore its application to non-cancer endpoints, we encountered a lack of data that are required for better-substantiated conclusions regarding differences in exposure between products. In this special communication, we argue the case for more data on adverse health effects, as well as more data on the composition of the emissions from tobacco products. Such information can be used to identify significant changes in relevance to health using the cumulative exposure method with different products and to substantiate regulatory decisions.Publisher PDFPeer reviewe

    Cigarettes sold in China: design, emissions and metals

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    Background China is the home to the world's largest cigarette maker, China National Tobacco Company (CNTC), yet little is known publicly about the design and emissions of Chinese cigarettes. CNTC is currently in the process of consolidating its brands and has ambitions to export its cigarettes. Machine-measured tar yields of many of its cigarette brands have also been reduced, similar to what occurred in Western countries from the 1970s through the 1990s with so-called 'low-tar' cigarettes introduced to address consumer concerns about health risks from smoking.Method The current study examines the design and physical characteristics, labelled smoke emissions and tobacco metals content of leading brands of Chinese cigarettes from seven cities purchased in 2005-6 and in 2007.Results Findings suggest that similar to most countries, tar levels of Chinese cigarettes are predicted primarily by tobacco weight and filter ventilation. Ventilation explained approximately 50% of variation observed in tar and 60% variation in carbon monoxide yields. We found little significant change in key design features of cigarettes purchased in both rounds. We observed significant levels of various metals, averaging 0.82 mu g/g arsenic (range 0.3-3.3), 3.21 mu g/g cadmium (range 2.0-5.4) and 2.65 mu g/g lead (range 1.2-6.5) in a subsample of 13 brands in 2005-6, substantially higher than contemporary Canadian products.Conclusion Results suggest that cigarettes in China increasingly resemble those sold in Western countries, but with tobacco containing higher levels of heavy metals. As CNTC looks to export its product around the world, independent surveillance of tobacco product characteristics, including tobacco blend characteristics, will become increasingly important.</p

    Kinetically induced compositional zoning in titanite:implications for accessory-phase/melt partitioning of trace elements

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    Usually it is assumed that the partitioning of trace elements into titanite in metaluminous granitoid plutonic environments takes place under equilibrium conditions and that compositional zoning is due solely to progressive changes in melt chemistry and/or mineral/melt partition coefficients. Examination of titanites from a variety of Caledonian metaluminous granitoids and related rocks has revealed that sector zoning is present, indicating disequilibrium partitioning. The sector zoning in titanites is defined principally by the distribution of the rare earth elements (REE), Y, Nb, Al and Fe. The REE, Y and Nb preferentially occur within the minor (100) sectors relative to the morphologically important (111) sectors. The reverse is true of Al and Fe which preferentially occur within the (111) sectors relative to the (100) sectors. The patterns of sector zoning are complicated by the fact that the relative growth rates of the various crystal faces fluctuated during growth. Sector zoning indicates that crystal-interface kinetics are responsible for the observed patterns of element partitioning. It is concluded that differences in the lateral-layerspreading rates of crystal faces bring about the sector zoning. The results have implications for the use of trace element partition coefficients in the modelling of fractionation processes.</p

    Kinetically induced compositional zoning in titanite:implications for accessory-phase/melt partitioning of trace elements

    No full text
    Usually it is assumed that the partitioning of trace elements into titanite in metaluminous granitoid plutonic environments takes place under equilibrium conditions and that compositional zoning is due solely to progressive changes in melt chemistry and/or mineral/melt partition coefficients. Examination of titanites from a variety of Caledonian metaluminous granitoids and related rocks has revealed that sector zoning is present, indicating disequilibrium partitioning. The sector zoning in titanites is defined principally by the distribution of the rare earth elements (REE), Y, Nb, Al and Fe. The REE, Y and Nb preferentially occur within the minor (100) sectors relative to the morphologically important (111) sectors. The reverse is true of Al and Fe which preferentially occur within the (111) sectors relative to the (100) sectors. The patterns of sector zoning are complicated by the fact that the relative growth rates of the various crystal faces fluctuated during growth. Sector zoning indicates that crystal-interface kinetics are responsible for the observed patterns of element partitioning. It is concluded that differences in the lateral-layerspreading rates of crystal faces bring about the sector zoning. The results have implications for the use of trace element partition coefficients in the modelling of fractionation processes.</p

    Evidence for inherited Sm-Nd isotopes in granitoid zircons

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    This study presents evidence to show that, in addition to preserving U-Pb isotope systematics, refractory zircons also preserve, at least in part, an inherited Sm-Nd isotope component. The zircons analyzed during this study were taken from the Strontian granitoid (NW Scotland). The inner intrusion of this composite pluton is known from a previous study to contain substantial U-Pb zircon inheritance, whereas the outer part has only minor inheritance. Zircons from the inner intrusion were found to have significantly lower εNd425 values than either their host rock, separated apatite or monazite. It is argued that this isotopic disequilibrium is due to the presence of an inherited Sm-Nd isotope component, rather than being due to a post-crystallization disturbance of the zircons. The preservation of inherted Sm-Nd isotopes within refractory zircons implies that they remain closed systems with respect to the diffusion of Sm and Nd (and presumably the other REE) to temperatures in excess of 700°C. The fact that zircons commonly have high Sm/Nd ratios, relative to sialic crustal material, means that the Nd isotopic evolution of inherited zircons will be very different to that of much of the continental crust.</p
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