Nicotine flux as a powerful tool for regulating nicotine delivery from e-cigarettes: Protocol of two complimentary randomized crossover clinical trials

• Published in: PloS one 2023-09, Vol.18 (9), p.e0291786-e0291786
• Main Authors: El-Hellani, Ahmad, Hanna, Elyana, Sharma, Mehak, Blohowiak, Reagan, Joseph, Phillip, Eid, Tore, Nadim, Haleh, El-Hage, Rachel, Salman, Rola, Karaoghlanian, Nareg, Adeniji, Ayomipo, Salam, Sally, Talih, Farid, Elbejjani, Martine, Breland, Alison, Eissenberg, Thomas, Shihadeh, Alan, Baldassarri, Stephen R, Talih, Soha
• Format: Article
• Language: English
• Subjects: Abstinence; Adolescent; Biological Transport; Biology and Life Sciences; Cigarettes; Clinical trials; Crack (Drug); Craving; Cross-Over Studies; Distribution; Drug dosages; Drugs and youth; Electronic cigarettes; Electronic Nicotine Delivery Systems; Emissions (Pollution); Evaluation; Fluctuations; Health aspects; Humans; Liability; Mathematical models; Medical colleges; Medicine and Health Sciences; Nicotine; Physical Sciences; Power; Research and Analysis Methods; Social Sciences; Study Protocol; Teenagers; Tobacco; Toxicants; Youth
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0291786

Electronic cigarette (EC) use has increased rapidly in the last decade, especially among youth. Regulating nicotine delivery from ECs could help curb youth uptake and leverage EC use in harm reduction yet is complicated by varying device and liquid variables that affect nicotine delivery. Nicotine flux, the nicotine emission rate, is a parameter that incorporates these variables and focuses on the performance rather than the design of an EC. Nicotine flux therefore could be a powerful regulatory tool if it is shown empirically to predict nicotine delivery and subjective effects related to dependence. This project consists of two complementary clinical trials. In Trial I, we will examine the relationship between nicotine flux and the rate and dose of nicotine delivery from ECs, hence, impacting abuse liability. It will also examine the extent to which this relationship is mediated by nicotine form (i.e., freebase versus protonated). At Yale School of Medicine (YSM), study participants will puff EC devices under conditions that differ by flux and form, while arterial blood is sampled in high time resolution. In Trial II, we will assess the relationship between nicotine flux, form, and subjective effects. At the American University of Beirut (AUB), participants will use EC devices with varying nicotine fluxes and forms, while dependency measures, such as the urge to use ECs, nicotine craving, and withdrawal symptoms, will be assessed. We will also monitor puffing intensity and real-time exposure to toxicants. The protocol of Trial I and Trial II was approved by YSM and AUB IRBs, respectively. We will disseminate study results through peer-reviewed publications and conference presentations. NCT05706701 for Trial I and NCT05430334 for Trial II.