This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.Objective: To compare nicotine pharmacokinetics and subjective effects of three newer smokeless tobacco potential reduced exposure products (PREPs; Ariva, Revel, Stonewall) to moist snuff (Copenhagen) and medicinal nicotine (Commit lozenge).Methods: Ten subjects completed a randomized, within-subject, cross-over study. Subjects used one product for 30 minutes at each of five laboratory sessions. Maximal nicotine concentration (Cmax) was determined and area under the concentration time curve (AUC) was calculated for a 90 minute period (during use and 60 minutes post-use). Nicotine craving, withdrawal symptoms and ratings of product effects and liking were measured during product use.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000400-40
Application #
7717384
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2007-12-01
Project End
2008-11-30
Budget Start
2007-12-01
Budget End
2008-11-30
Support Year
40
Fiscal Year
2008
Total Cost
$7,510
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
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