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1.
Sci Rep ; 10(1): 7160, 2020 04 28.
Article in English | MEDLINE | ID: mdl-32345986

ABSTRACT

Recent increases in marijuana use and legalization without adequate knowledge of the risks necessitate the characterization of the billions of nanoparticles contained in each puff of smoke. Tobacco smoke offers a benchmark given that it has been extensively studied. Tobacco and marijuana smoke particles are quantitatively similar in volatility, shape, density and number concentration, albeit with differences in size, total mass and chemical composition. Particles from marijuana smoke are on average 29% larger in mobility diameter than particles from tobacco smoke and contain 3.4× more total mass. New measurements of semi-volatile fractions determine over 97% of the mass and volume of the particles from either smoke source are comprised of semi-volatile compounds. For tobacco and marijuana smoke, respectively, 4350 and 2575 different compounds are detected, of which, 670 and 536 (231 in common) are tentatively identified, and of these, 173 and 110 different compounds (69 in common) are known to cause negative health effects through carcinogenic, mutagenic, teratogenic, or other toxic mechanisms. This study demonstrates striking similarities between marijuana and tobacco smoke in terms of their physical and chemical properties.


Subject(s)
Cannabis/chemistry , Nicotiana/chemistry , Smoke/analysis , Gas Chromatography-Mass Spectrometry , Volatilization
2.
J Chromatogr A ; 1603: 327-337, 2019 Oct 11.
Article in English | MEDLINE | ID: mdl-31266643

ABSTRACT

An analytical methodology based on thermal desorption and comprehensive two-dimensional gas chromatography with dual time-of-flight mass spectrometry and flame ionization detection (TD-GC × GC-TOFMS/FID) has been developed for non-target analysis of volatile organic compounds (VOCs). The technique was optimised for the measurement of the VOC content of the particulate phase (PP) fraction of aerosols produced by a tobacco heating product (THP1.0) and 3R4F mainstream tobacco smoke (MTS). The method involves sampling the PP fraction on quartz wool packed in a sorbent tube directly connected to machine-puffing, followed by a dilution through a TD recollection procedure over Tenax/Sulficarb sorbent before TD-GC × GC-TOFMS/FID analysis. The comparison of the VOC content of the PP fraction of aerosols produced by THP1.0 and MTS highlighted the compositional difference between tobacco combustion (592 peaks) and tobacco heating process (160 peaks). Mass spectrometric signals were used for qualitative analyses based on linear retention indices, mass spectral matches, and GC × GC structured chromatograms, which collectively identified up to 90% of analytes detected in PP samples. FID signals were used for semi-quantitative analyses based on a chemical class external calibration method. The global chemical composition of PP samples showed that hydrocarbons, oxygenated, and nitrogen-containing compounds were fewer in number and much less abundant in THP1.0 PP. Overall, 93 compounds were common to the two sample types. Excepted for a few highly volatile compounds (mainly furan family) as well as glycerine and its acetate, analyte concentrations were higher in MTS PP.


Subject(s)
Aerosols/analysis , Flame Ionization/methods , Gas Chromatography-Mass Spectrometry/methods , Particulate Matter/analysis , Temperature , Tobacco Products/analysis , Signal-To-Noise Ratio , Volatile Organic Compounds/analysis
3.
J Chromatogr A ; 1581-1582: 105-115, 2018 Dec 21.
Article in English | MEDLINE | ID: mdl-30455053

ABSTRACT

A simple direct sample collection/dilution and introduction method was developed using quartz wool and Tenax/sulficarb sorbents for thermal desorption and comprehensive two-dimensional gas chromatography (TD-GC × GC) analyses of volatile organic compounds from vapour phase (VP) fractions of aerosol produced by tobacco heating products (THP1.0) and 3R4F mainstream tobacco smoke (MTS). Analyses were carried out using flame ionisation detection (FID) for semi-quantification and both low and high resolution time-of-flight mass spectrometry (LR/HR-TOFMS) for qualitative comparison and peak assignment. Qualitative analysis was carried out by combining identification data based on linear retention indices (LRIs) with a match window of ±10 index units, mass spectral forward and reverse library searches (from LR and HRTOFMS spectra) with a match factor threshold of >700 (both forward and reverse), and accurate mass values of ± 3 ppm for increased confidence in peak identification. Using this comprehensive approach of data mining, a total of 79 out of 85 compounds and a total of 198 out of 202 compounds were identified in THP1.0 aerosol and in 3R4F MTS, respectively. Among the identified analytes, a set of 35 compounds was found in both VP sample types. Semi-quantitative analyses were carried out using a chemical class-based external calibration method. Acyclic, alicyclic, aromatic hydrocarbons and ketones appeared to be prominent in 3R4F MTS VP, whereas larger amounts of aldehydes, ketones, heterocyclic hydrocarbons and esters were present in THP1.0 aerosol VP. The results demontsrate the capability and versatility of the method for the characterization and comparison of complex aerosol samples and highlighted the relative chemical simplicity of THP1.0 aerosol in comparison to MTS.


Subject(s)
Aerosols/chemistry , Chemistry Techniques, Analytical/methods , Nicotiana/chemistry , Smoke/analysis , Gases/analysis , Heating , Tobacco Products/analysis , Volatile Organic Compounds/analysis
4.
J Chromatogr A ; 1525: 126-137, 2017 Nov 24.
Article in English | MEDLINE | ID: mdl-29030031

ABSTRACT

A thermal desorption comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (TD-GC×GC-TOFMS) method has been developed for the analysis of mainstream tobacco smoke (MTS) vapour phase (VP). The selection process of the sample introduction approach involved comparing the results obtained from three different approaches: a) use of gas sampling bag followed by SPME (Tedlar®-SPME), b) gas sampling bag followed by TD (Tedlar®-TD), and c) sampling directly on TD sorbents (Direct-TD). Six different SPME fibers and six different TD sorbent beds were evaluated for the extraction capacities in terms of total number of peaks and related intensities or peak areas. The best results were obtained for the Direct-TD approach using Tenax TA/Carbograph1TD/Carboxen1003 sorbent tubes. The optimisation of TD tube desorption parameters was carried out using a face-centered central composite experimental design and resulted in the use of the Tenax TA/Carbograph 1TD/Carboxen 1003 sorbent with a 7.5min desorption time, a 60mL/min tube desorption flow, and a 250°C tube desorption temperature. The optimised method was applied to the separation of MTS-VP constituents, with 665 analytes detected. The method precision ranged from 1% to 15% for over 99% of identified peak areas and from 0% to 3% and 0% to 1% for both first (1tR) and second (2tR) dimension retention times, respectively. The method was applied to the analyses of two cigarette types differing in their filter construction. Principal component analysis (PCA) allowed a clear differentiation of the studied cigarette types (PC1 describing 94% of the explained variance). Supervised Fisher ratio analysis permitted the identification of compounds responsible for the chemical differences between the two sample types. A set of 91 most relevant compounds was selected by applying a Fisher ratio cut-off approach and most of them were selectively removed by one of the cigarette filter types.


Subject(s)
Chemistry Techniques, Analytical/methods , Gas Chromatography-Mass Spectrometry , Nicotiana/chemistry , Smoke/analysis , Gases/analysis , Polymers/chemistry , Principal Component Analysis , Volatile Organic Compounds/analysis
5.
J Chromatogr A ; 1520: 135-142, 2017 Oct 20.
Article in English | MEDLINE | ID: mdl-28911941

ABSTRACT

A method involving headspace solid-phase microextraction (HS-SPME) and comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC×GC-TOFMS) was developed and optimised to elucidate the volatile composition of the particulate phase fraction of aerosol produced by tobacco heating products (THPs). Three SPME fiber types were studied in terms of extraction capacity and precision measurements. Divinylbenzene polydimethylsiloxane appeared as the most efficient coating for these measurements. A central composite design of experiment was utilised for the optimization of the extraction conditions. Qualitative and semi-quantitative analysis of the headspace above THP aerosol condensate was carried out using optimised extraction conditions. Semi-quantitative analyses of detected constituents were performed by assuming that their relative response factors to the closest internal standard (itR) were equal to 1. Using deconvoluted mass spectral data (library similarity and reverse match >750) and linear retention indices (match window of ±15 index units), 205 peaks were assigned to individual compounds, 82 of which (including 43 substances previously reported to be present in tobacco) have not been reported previously in tobacco aerosol. The major volatile fraction of the headspace contained ketones, alcohols, aldehydes, alicyclic hydrocarbons alkenes, and alkanes. The method was further applied to compare the volatiles from the particulate phase of aerosol composition of THP with that of reference cigarette smoke and showed that the THP produced a less complex chemical mixture. This new method showed good efficiency and precision for the peak areas and peak numbers from the volatile fraction of aerosol particulate phase for both THP and reference cigarettes.


Subject(s)
Aerosols/chemistry , Chemistry Techniques, Analytical/instrumentation , Chemistry Techniques, Analytical/methods , Gas Chromatography-Mass Spectrometry , Nicotiana/chemistry , Solid Phase Microextraction , Dimethylpolysiloxanes/chemistry , Heating , Polyvinyls/chemistry , Smoke
6.
J Chromatogr A ; 1365: 183-90, 2014 Oct 24.
Article in English | MEDLINE | ID: mdl-25249490

ABSTRACT

A multiplexed dual-primary column comprehensive two-dimensional gas chromatography-mass spectrometry approach (2GC×GC-MS) is introduced. The approach splits injected samples into two first-dimension columns with different stationary phases, and recombines the two streams into one second-dimension column that terminates at a single detector. The approach produces two two-dimensional chromatograms for each injection, and is made possible by using a dual-stage modulator operated in contra-directional modulation mode. The dual two-dimensional chromatograms produced by this single detector system provide complementary information due to selectivity differences between the three separation columns used in the column ensemble. An aged Australian tea tree (Melaleuca alternifolia) essential oil was analyzed to demonstrate the 2GC×GC-MS approach. The number of compounds separated by each of the GC×GC separations in the 2GC×GC experiment is comparable to conventional GC×GC experiments with matching column configurations. Robust peak assignment was possible for this sample based on the combination of MS library matches and multiple linear retention index searching. Forty-nine components (22 unique) were identified using a non-polar×mid-polar column combination and 34 components (7 unique) were positively identified using a polar×mid-polar column combination. Twenty-seven peak assignments were corroborated by positive identification in both of the multiplexed separations.


Subject(s)
Gas Chromatography-Mass Spectrometry/methods , Tea Tree Oil/analysis , Australia , Melaleuca/chemistry
7.
Anal Chim Acta ; 803: 160-5, 2013 Nov 25.
Article in English | MEDLINE | ID: mdl-24216210

ABSTRACT

A multiplexed dual-secondary column comprehensive two-dimensional gas chromatography approach (GC×2GC) designed for complex sample analysis is introduced. The approach splits the first-dimension column effluent into two second-dimension columns with different stationary phases, and recombines the two streams into one detector post-separation. The approach produces two single two-dimensional chromatograms for each injection. Careful manipulation of thermal modulator timing parameters combined with a novel contra-directional modulation regime facilitates this approach. A selection of 34 laboratory reference compounds containing n-alkanes, alcohols, aromatic hydrocarbons, ketones, esters and halogenated hydrocarbons were analysed to demonstrate the approach. The dual two-dimensional chromatogram from this single detector system provides complementary information due to the unique selectivity of the three separation columns. The results of this proof-of-principle investigation provide significant impetus for further development of GC×2GC-MS methodology.


Subject(s)
Chromatography, Gas/instrumentation , Alcohols/analysis , Alkanes/analysis , Equipment Design , Hydrocarbons, Aromatic/analysis , Hydrocarbons, Halogenated/analysis , Ketones/analysis , Temperature
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