Te Xu
Research Subjects
Research Interests
Te Xu has a total of 15 co-authors. Here are the top co-authors by number of shared publications:
- Bin Li
Zhengzhou Tobacco Research Institute of CNTC, Zhengzhou 450001, China
1 shared publication Chuan Liu
Zhengzhou Tobacco Research Institute of CNTC , Zhengzhou , China
1 shared publicationJiakai Liu
RELX Science Center, Shenzhen RELX Tech. Co,. Ltd ., Shenzhen , China
1 shared publicationJie Zhou
RELX Science Center, Shenzhen RELX Tech. Co,. Ltd ., Shenzhen , China
1 shared publicationJingjing Liang
RELX Science Center, Shenzhen RELX Tech. Co,. Ltd ., Shenzhen , China
1 shared publicationJunjun Luo
RELX Science Center, Shenzhen RELX Tech. Co,. Ltd ., Shenzhen , China
1 shared publication
Latest Publications
- Open Access
- 1 December 2023
- Published by Walter de Gruyter GmbH in Contributions to Tobacco & Nicotine Research
- Vol. 32 (4) , 146-156
A Comparative In Vitro Toxicological Screening of a Closed-End Heated Tobacco Product *
SUMMARY: Heated tobacco products (HTPs) are a recent category of tobacco products, with their relative safety compared to cigarette smoking and potential to help smokers to quit being two reasons why regulators may consider their market approval. Designed to heat tobacco rather than to burn in order to produce aerosol, different heating techniques are applied to commercial HTPs, which may result in differing aerosol formation. Therefore, each product requires separate assessment. This work focuses on a closed-end HTP (coded as HTP-A), which is electrically heated and designed to allow puffing air flow to bypass its tobacco section, resulting in reduced oxygen concentration within the tobacco section during heating and aerosol forming. To provide a preliminary aerosol chemistry and in vitro toxicological screening, this study assessed HTP-A against a commercial electrically heated HTP (IQOS TM , coded as HTP-B) and a 3R4F reference cigarette. Under Health Canada Intense (HCI) smoking regime, the levels of 9 regulatory priority toxicants in the aerosol of HTP-A were either reduced or comparable to those in HTP-B on a per-stick basis. Additionally, both HTPs showed significant reduction (greater than 90%) in comparison to those measured in mainstream smoke of 3R4F cigarette for these toxicants. Using a set of standard in vitro toxicological assays (Ames, Micronucleus and Neutral Red Uptake), the two HTPs showed no observable responses while significant toxicity responses were recorded for 3R4F’s total particulate matter. Based on these preliminary results, the novel closed-end HTP-A design may provide similar toxicological profiles to the comparator HTP-B. Further toxicological and clinical assessments are warranted to evaluate HTP-A’s potential for exposure or disease risk reduction. [Contrib. Tob. Nicotine Res. 32 (2023) 146–156]
- 1 December 2023
- Published by Walter de Gruyter GmbH in Contributions to Tobacco & Nicotine Research
- Vol. 32 (4) , 146-156
Open AccessA Comparative In Vitro Toxicological Screening of a Closed-End Heated Tobacco Product *
SUMMARY: Heated tobacco products (HTPs) are a recent category of tobacco products, with their relative safety compared to cigarette smoking and potential to help smokers to quit being two reasons why regulators may consider their market approval. Designed to heat tobacco rather than to burn in order to produce aerosol, different heating techniques are applied to commercial HTPs, which may result in differing aerosol formation. Therefore, each product requires separate assessment. This work focuses on a closed-end HTP (coded as HTP-A), which is electrically heated and designed to allow puffing air flow to bypass its tobacco section, resulting in reduced oxygen concentration within the tobacco section during heating and aerosol forming. To provide a preliminary aerosol chemistry and in vitro toxicological screening, this study assessed HTP-A against a commercial electrically heated HTP (IQOS TM , coded as HTP-B) and a 3R4F reference cigarette. Under Health Canada Intense (HCI) smoking regime, the levels of 9 regulatory priority toxicants in the aerosol of HTP-A were either reduced or comparable to those in HTP-B on a per-stick basis. Additionally, both HTPs showed significant reduction (greater than 90%) in comparison to those measured in mainstream smoke of 3R4F cigarette for these toxicants. Using a set of standard in vitro toxicological assays (Ames, Micronucleus and Neutral Red Uptake), the two HTPs showed no observable responses while significant toxicity responses were recorded for 3R4F’s total particulate matter. Based on these preliminary results, the novel closed-end HTP-A design may provide similar toxicological profiles to the comparator HTP-B. Further toxicological and clinical assessments are warranted to evaluate HTP-A’s potential for exposure or disease risk reduction. [Contrib. Tob. Nicotine Res. 32 (2023) 146–156]