Key challenges for in vitro testing of tobacco products for regulatory applications: Recommendations for dosimetry.


Journal

Drug testing and analysis
ISSN: 1942-7611
Titre abrégé: Drug Test Anal
Pays: England
ID NLM: 101483449

Informations de publication

Date de publication:
Oct 2023
Historique:
revised: 02 07 2022
received: 18 03 2022
accepted: 05 07 2022
pmc-release: 13 01 2024
medline: 8 11 2023
pubmed: 14 7 2022
entrez: 13 7 2022
Statut: ppublish

Résumé

The Institute for In Vitro Sciences (IIVS) is sponsoring a series of workshops to develop recommendations for optimal scientific and technical approaches for conducting in vitro assays to assess potential toxicity within and across tobacco and various next-generation products (NGPs) including heated tobacco products (HTPs) and electronic nicotine delivery systems (ENDSs). This publication was developed by a working group of the workshop members in conjunction with the sixth workshop in that series entitled "Dosimetry for conducting in vitro evaluations" and focuses on aerosol dosimetry for aerosol exposure to combustible cigarettes, HTP, and ENDS aerosolized tobacco products and summarizes the key challenges as well as documenting areas for future research.

Identifiants

pubmed: 35830202
doi: 10.1002/dta.3344
pmc: PMC9897201
mid: NIHMS1865971
doi:

Substances chimiques

Aerosols 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1175-1188

Subventions

Organisme : FDA HHS
ID : R13 FD007386
Pays : United States
Organisme : FDA HHS
ID : 1R13D007386
Pays : United States
Organisme : FDA HHS
ID : 1R13D007386
Pays : United States

Informations de copyright

© 2022 JT International SA and The Authors. Drug Testing and Analysis published by John Wiley & Sons Ltd.

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Auteurs

Jacqueline Miller-Holt (J)

Scientific & Regulatory Affairs, JT International SA, Geneva, Switzerland.

Holger Behrsing (H)

Institute for In Vitro Sciences, Gaithersburg, Maryland, USA.

Ian Crooks (I)

Consumer Product Safety, British American Tobacco, Southampton, UK.

Rodger Curren (R)

Institute for In Vitro Sciences, Gaithersburg, Maryland, USA.

Kubilay Demir (K)

Regulatory Science, JUUL Labs Inc., 1000 F Street NW, Washington D.C., 20004, USA.

Jeremie Gafner (J)

Scientific & Regulatory Affairs, JT International SA, Geneva, Switzerland.

Gene Gillman (G)

Regulatory Science, JUUL Labs Inc., 1000 F Street NW, Washington D.C., 20004, USA.

Michael Hollings (M)

Genetic Toxicology, Labcorp Early Development Laboratories Ltd., Harrogate, UK.

Robert Leverette (R)

Scientific & Regulatory Affairs, RAI Services Company, Winston-Salem, North Carolina, USA.

Michael Oldham (M)

Regulatory Science, JUUL Labs Inc., 1000 F Street NW, Washington D.C., 20004, USA.

Liam Simms (L)

Group Science and Regulatory Affairs, Imperial Brands, Bristol, UK.

Leon F Stankowski (LF)

Genetic and In Vitro Toxicology, Charles River Laboratories-Skokie, Skokie, Illinois, USA.

David Thorne (D)

Consumer Product Safety, British American Tobacco, Southampton, UK.

Roman Wieczorek (R)

Group Science and Regulatory Affairs, Reemtsma Cigarettenfabriken GmbH, an Imperial Brands PLC Company, Hamburg, Germany.

Martha M Moore (MM)

Martha M Moore LLC, Little Rock, Arkansas, USA.

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