Table 1.
Detects | Cutpoint | Average half-life | Approximate time to cutpoint |
||
---|---|---|---|---|---|
Free cotinine plasma, saliva, and urinea | Exposure to nicotine from all sources (e.g., combustible, noncombustible, and NRT) | 3–10 ng/ml 30–50 ng/ml |
16 h | 80–100 h | |
CO (exhaled air) | Consumption of combustible tobacco and nontobacco (e.g., marijuana) products | 5–6 ppmb | 2–8 h depends on physical activity level |
12–24 h | |
Minor tobacco alkaloids (urine) | Exposure to tobacco-derived nicotine products (e.g., cigarettes, cigars, and smokeless) | Anabasine Anatabine Nicotelline |
2 ng/ml 2 ng/ml ? |
16 h 10 h 2–3 h |
80 h 50 h 10 h |
NNAL (urine) | Exposure to cured tobacco (e.g., cigarrettes, cigars, and smokeless) | 10–40 pg/ml | 10–40 days | 2–3 months |
NNAL = 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol; NRT = nicotine replacement therapy.
Urine provides the highest concentration of cotinine and, thus, has the greatest sensitivity but also more between-sample variability. Plasma and saliva provide similar results, with lower concentrations, but with more between-sample stability.
At one end of the continuum (e.g., in a country with high smoking prevalence and relatively weak legislation requiring smoke-free public places in industrial cities with high levels of air pollution), we recommend that the previous cutpoint of <10 ppm to validate a self-report of smoking abstinence for at least 24 h may still be appropriate. At the other end of the continuum (e.g., in places with strong smoke-free legislation, low smoking prevalence and relatively low levels of air pollution), we recommend that a cutpoint as low as <5 ppm will be more appropriate. Investigators should select the appropriate cutpoint (from 4 to 10 ppm) for their research and clinical purposes bearing these known factors (as well as brand/model of monitor) in mind.25