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


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 26 07 2023
accepted: 07 08 2023
medline: 25 9 2023
pubmed: 21 9 2023
entrez: 21 9 2023
Statut: epublish

Résumé

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.

Identifiants

pubmed: 37733666
doi: 10.1371/journal.pone.0291786
pii: PONE-D-23-19513
pmc: PMC10513228
doi:

Substances chimiques

Nicotine 6M3C89ZY6R

Banques de données

ClinicalTrials.gov
['NCT05430334', 'NCT05706701']

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0291786

Subventions

Organisme : NIDA NIH HHS
ID : R01 DA052565
Pays : United States
Organisme : NIDA NIH HHS
ID : U54 DA036105
Pays : United States

Informations de copyright

Copyright: © 2023 El-Hellani et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

AS and TEissenberg are paid consultants in litigation against the tobacco and EC industry and are named on a patent for a device that measures the puffing behavior of EC users and another patent application for a smoking cessation intervention. TEissenberg is also named on a patent application for a smartphone app that determines EC device and liquid characteristics. All other authors declare no conflict of interest. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Ahmad El-Hellani (A)

Division of Environmental Health Sciences, College of Public Health, The Ohio State University, Columbus, Ohio, United States of America.
Center for Tobacco Research, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States of America.

Elyana Hanna (E)

Department of Mechanical Engineering, Maroun Semaan Faculty of Engineering and Architecture, American University of Beirut, Beirut, Lebanon.
Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.

Mehak Sharma (M)

Section of Pulmonary, Critical Care, and Sleep Medicine, Yale School of Medicine, New Haven, Connecticut, United States of America.

Reagan Blohowiak (R)

Section of Pulmonary, Critical Care, and Sleep Medicine, Yale School of Medicine, New Haven, Connecticut, United States of America.

Phillip Joseph (P)

Section of Pulmonary, Critical Care, and Sleep Medicine, Yale School of Medicine, New Haven, Connecticut, United States of America.

Tore Eid (T)

Department of Laboratory Medicine, Yale School of Medicine, Washington, DC, United States of America.

Haleh Nadim (H)

Department of Laboratory Medicine, Yale School of Medicine, Washington, DC, United States of America.

Rachel El-Hage (R)

Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Department of Chemistry, Faculty of Arts and Sciences, American University of Beirut, Beirut, Lebanon.

Rola Salman (R)

Department of Mechanical Engineering, Maroun Semaan Faculty of Engineering and Architecture, American University of Beirut, Beirut, Lebanon.
Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.

Nareg Karaoghlanian (N)

Department of Mechanical Engineering, Maroun Semaan Faculty of Engineering and Architecture, American University of Beirut, Beirut, Lebanon.
Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.

Ayomipo Adeniji (A)

Division of Environmental Health Sciences, College of Public Health, The Ohio State University, Columbus, Ohio, United States of America.
Center for Tobacco Research, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States of America.

Sally Salam (S)

Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Department of Chemistry, Faculty of Arts and Sciences, American University of Beirut, Beirut, Lebanon.

Farid Talih (F)

Clinical Psychiatry, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.

Martine Elbejjani (M)

Clinical Research Institute & Department of Internal Medicine, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.

Alison Breland (A)

Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Department of Psychology, Virginia Commonwealth University, Richmond, Virginia, United States of America.

Thomas Eissenberg (T)

Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Department of Psychology, Virginia Commonwealth University, Richmond, Virginia, United States of America.

Alan Shihadeh (A)

Department of Mechanical Engineering, Maroun Semaan Faculty of Engineering and Architecture, American University of Beirut, Beirut, Lebanon.
Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.

Stephen R Baldassarri (SR)

Section of Pulmonary, Critical Care, and Sleep Medicine, Yale School of Medicine, New Haven, Connecticut, United States of America.
Yale Center for the Study of Tobacco Product Use and Addiction, Yale University, New Haven, Connecticut, United States of America.
Program in Addiction Medicine, Yale School of Medicine, Washington, DC, United States of America.

Soha Talih (S)

Department of Mechanical Engineering, Maroun Semaan Faculty of Engineering and Architecture, American University of Beirut, Beirut, Lebanon.
Center for the Study of Tobacco Products, Virginia Commonwealth University, Richmond, Virginia, United States of America.

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