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Tobacco alkaloids are important precursors of carcinogenic tobacco-specific nitrosamines. Therefore, accurate quantification of tobacco alkaloids is highly important. This study investigates the compensation effects of novel analyte protectants (APs) for matrix effects (MEs) to determine seven minor tobacco alkaloids (nornicotine, myosmine, anabasine, anatabine, nicotyrine, 2,3'-bipyridine, and cotinine) in mainstream cigarette smoke with high accuracy and robustness. By comparing the heights and shapes of the chromatographic peaks before and after the addition of APs to standard solutions prepared in dichloromethane and cigarette smoke solutions, the compensation effects of 12 APs and their combinations on the MEs of seven minor tobacco alkaloids were evaluated, and the best combination of 2-pyridylethylamine (2 mg/mL)+1,2-decanediol (1 mg/mL) was identified. This AP combination could effectively improve the shapes and increase the heights (by 7-371%) of chromatographic peaks for standard solutions prepared in dichloromethane and cigarette smoke solutions. Before the addition of this AP combination, the slope ratios of the calibration curves for two types of standard solutions of the seven target chemicals were 71.4-159.8%, while they were 87.4-105.6% after the addition, indicating that this AP combination reduced the matrix difference between pure solvent and cigarette smoke solution. After adding the AP combination, the standard curves of solutions prepared in dichloromethane showed good linearity (r 2 ≥ 0.999), the spiked recoveries were between 80.9% and 119.6%, and the inter- and intraday precisions were between 1.5-9.5% and 3.1-8.5%, respectively. Three commercial cigarette samples and one mixed standard solution were also tested under four different instrument working conditions to verify the long-term accuracy and ruggedness of the approach in routine real-world analysis of the method. The results showed that the RSD values were higher (3.5-25.4%) without the AP combination than that (<6.7%) with the AP combination. Because of its high accuracy, precision, and robustness, this method has good practical prospects., Competing Interests: Declaration of Competing Interest There are no conflicts of interest., (Copyright © 2022. Published by Elsevier B.V.)

Heated tobacco products and electronic cigarettes are considered as alternatives to traditional tobacco cigarettes. However, it is crucial to monitor and compare the nicotine concentration in inhaled aerosols from these tobacco products, owing to the addictive nature and adverse effects of nicotine on human health. This study aimed to provide an electromembrane extraction (EME) combined liquid chromatography method to extract and determine nicotine in different inhaled aerosols. EME showed high extraction efficiency, selectivity, and sample clean-up capability. Under the optimal parameters, the linear range for nicotine was 0.1-200 mg L -1 (r 2  > 0.9998), and the limit of detection was 0.02 mg L -1 . Good precision was obtained with the intra- and inter-day relative standard deviations of 2.2 % and 2.8 %, respectively. Repeatability was satisfactory (<7.7 %), and recoveries ranged from 81.0 % to 112.8 %. Finally, this method has been successfully used for the determination and comparison of nicotine in aerosols from these three tobacco products., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

According to the normal production conditions, 13 kinds of n-alkanes were added to the core material sheet production process to prepare heated tobacco products, and a GC-MS analysis method suitable for re-alkanes in the core material, filter and mainstream smoke particulate matter of heated tobacco products was established. The transfer behavior of re-alkanes in heated tobacco products was studied by measuring the content, release and mouth-to-mouth release of re-alkanes in heated tobacco products. The results showed that: 1) The particle phase transfer rates of 13 re-alkanes in mainstream smoke were 0~53. 5 %, the filter interception rate was 12. 6% ~ 50. 0%, the smoke support retention rate was 0. 2% ~ 35. 4%, the smoke core residue rate was 6. 4% ~ 29. 3%, and the loss rate was 0. 6% ~ 81. 5%; With the increase of relative molecular mass and boiling point, the transfer rate of particulate matter and the interception rate of filter in mainstream smoke of n-alkane compounds increased first and then decreased, the residual rate of cigarette core increased gradually, and the retention rate of cigarette support increased first and then stabilized. The smoke retention rate and filter rejection rate showed a good positive correlation with the boiling point of the compound within a certain range. 2) With the increase of the number of suction ports, the release amount of re-alkanes increased first and then decreased, but the order of the maximum release amount was inconsistent. The lower the boiling point of the compound, the earlier the order of the maximum release amount. 3) The coefficient of variation of the puff-by-puff release of re-alkanes ranged from 0. 28 to 0. 44. The coefficient of variation of the puff-by-puff release of tridecane ( boiling point 235°C) and tetradecane ( boiling point 254 °C) was small, and the puff-by-puff release stability was good. Based on the evaluation data of the retention rate of re-alkanes in heated tobacco products, the transfer rate of particulate matter in mainstream smoke, and the stability of puff-by-puff release, the boiling point range of additives suitable for heated tobacco products was proposed to be about 250 °C. [ABSTRACT FROM AUTHOR]

In order to investigate the effect of different ventilation distribution on organic acid release from mainstream smoke of slim cigarette, the slim cigarette samples with different filter ventilation and cigarette paper air permeability were rolled, and the organic acid in mainstream smoke of samples were analyzed by GC-MS, the prediction models of organic acids release based on both filter and paper ventilation rate were established. The results were as follows: 26 kinds of organic acids were detected. With the increase of filter ventilation rate or paper ventilation rate, the decrease rate of organic acids with smaller molecular weight was higher, while that with larger molecular weight was smaller, and the effect of paper ventilation rate on the release of organic acids in cigarette smoke was greater than that of filter ventilation rate. When the total ventilation rate (V) was constant, the release of organic acids in cigarette smoke with high filter ventilation rate and low paper ventilation rate was higher than that with low filter ventilation rate and high paper ventilation rate. The prediction accuracy of the model of organic acid release was high, and the results further proved that the cigarette organic acid release was higher with the combination of high filter ventilation rate and low paper ventilation rate. [ABSTRACT FROM AUTHOR]

The CHIRALPAK-IC was used, and the mixed solution of V (re-hexane) : V (isopropanol) = 95 : 5 was used as the mobile phase, and diethylamine was used as the mobile phase additive. In normal phase chromatography mode, a chiral column-high performance liquid chromatography-diode array detector (HPLC-DAD ) method was developed for the separation and analysis of nicotine optical isomers in tobacco and tobacco products. The characterization and test results of this method indicated:) The linear relationship between S-( -)-nicotine and R-( +)-nicotine was in the range of 15 ~750 µg/mL and 0. 75 ~30. 00 µg/mL, respectively. The detection limit and limit of quantification were 0.2 mg/g and 0. 05 mg/g, respectively. 2) The precision of intra- and inter-day measurements of nicotine was less than 0. 85% and 4. 00%, respectively; the recovery rates of S-( - ) -nicotine and R-( + ) -nicotine were 94. 93% ~ 103. 70% and 92. 50% ~ 117. 50%, respectively. This indicated that the method had good precision and high recovery rate. Using this method to determine the nicotine optical isomers of 26 different types of tobacco and tobacco products, it was found that tobacco was mainly S-( - )-nicotine, only 6 samples were detected by R-( + )-nicotine. The proportion of nicotine quality was 0. 18% ~0.70% ; among the 10 finished cigarettes and their mainstream smoke, the proportion of R-( + )-nicotine in total cigarette smoke was higher than that of cigarette tobacco. [ABSTRACT FROM AUTHOR]

• Exogenous dietary AGEs have been suggested to increase health risk. • Oral use tobacco products are used as substitute for cigarette smoking due to their "reduced risk" and no second-hand smoke. • Thus, oral use tobacco products may increase AGEs intake due to their oral form of use. • To the best of our knowledge, no survey of CML and CEL levels in oral use tobacco products has been reported. • The free and total CML and CEL in different oral use tobacco products was determined in this work for the first time. • What's more, the relationship of CML (or CEL) and lysine, total amino acid, reducing carbohydrates was studied also. Exogenous dietary advanced glycation endproducts (AGEs) have been suggested to increase health risk. Oral use tobacco products are used as substitute for cigarette smoking due to their "reduced risk" and no second-hand smoke. They may increase AGEs intake due to their oral form of use. However, research on AGEs in oral use tobacco products is limited. A HPLC-MS/MS method was developed to survey free and total Nε-Carboxymethyllysine (CML) and Nε-Carboxyethyllysine (CEL) levels in different oral use tobacco products in this work. HPLC conditions, such as HPLC column and mobile phase additive were optimized. With the optimized conditions, analytical method performance for three types of oral use tobacco matrix (i.e. CRP2, gum and dissolvable tobacco product) was characterized. CML and CEL showed higher recovery in all three sample matrix, and the recovery of CML and CEL was in the range of 88.7%-120%, 90.0%-110%, respectively. The developed method showed good intra-day and inter-day precision with RSDs for both free and total CML (or CEL) of less than 9.7%. Limit of detections (LODs) of CML and CEL were 0.36 and 0.25 ng/mL, respectively. Sample analysis for 21 oral use tobacco products was conducted with the developed method. As for oral use tobacco products, total CML and CEL was much more than those of their free state, indicating that CML and CEL exist mainly protein adducts. In addition, the content of CML was higher than that of CEL for both free and total state. Oral use tobacco products I (i.e. dry snuff, moist snuff, suns and chew) had the highest CML (i.e. 44.89–608.69 µg/g) and CEL (i.e. 15.98–77.70 µg/g) levels, compared with oral use tobacco products II (i.e. gum) with the least CML (i.e. 0.7–0.8 µg/g) and CEL (i.e. 0.14–0.18 µg/g) levels. It mainly depended on the composition and processing technology of oral use tobacco products. Both total CML and CEL showed linear relationship with lysine and total amino acid (i.e. R > 0.77). However, there was no linear relationship between total CML (or CEL) and total reducing carbohydrates (i.e. R < 0.5). [ABSTRACT FROM AUTHOR]