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A biomonitoring assessment of secondhand exposures to electronic cigarette emissions

Supporting Files
File Language:
English


Details

  • Alternative Title:
    Int J Hyg Environ Health
  • Personal Author:
  • Description:
    Background:

    Electronic cigarette (e-cigarette) conventions regularly bring together thousands of users around the world. In these environments, secondhand exposures to high concentrations of e-cigarette emissions are prevalent. Some biomarkers for tobacco smoke exposure may be used to characterize secondhand e-cigarette exposures in such an environment.

    Methods:

    Participants who did not use any tobacco product attended four separate e-cigarette events for approximately six hours. Urine and saliva samples were collected from participants prior to the event, immediately after the event, 4-h after the event, and the next morning (first void). Urine samples from 34 participants were analyzed for cotinine, trans-3′-hydroxycotinine, S-(3-hydroxypropyl)-N-acetylcysteine (3-HPMA), S-carboxyethyl-N-acetylcysteine (CEMA), select tobacco-specific nitrosamines (TSNAs), and 8-isoprostane. Saliva samples were analyzed for cotinine and trans-3′-hydroxycotinine.

    Results:

    Data from 28 of 34 participants were used in the data analysis. Creatinine-adjusted urinary cotinine concentrations increased up to 13-fold and peaked 4-h after completed exposure (range of adjusted geometric means [AGMs] = 0.352–2.31 μg/g creatinine). Salivary cotinine concentrations were also the highest 4-h after completed exposure (range of AGMs = 0.0373–0.167 ng/mL). Salivary cotinine and creatinine-corrected concentrations of urinary cotinine, trans-3′-hydroxycotinine, CEMA, and 3-HPMA varied significantly across sampling times. Urinary and salivary cotinine, urinary trans-3′-hydroxycotinine, and urinary 3-HPMA concentrations also varied significantly across events.

    Conclusion:

    Secondhand e-cigarette exposures lasting six hours resulted in significant changes in exposure biomarker concentrations of both nicotine and acrolein but did not change exposure to tobacco-specific nitrosamines. Additional research is needed to understand the relationship between biomarker concentrations and environmental concentrations of toxicants in e-cigarette emissions.

  • Keywords:
  • Source:
    Int J Hyg Environ Health. 222(5):816-823
  • Pubmed ID:
    31085112
  • Pubmed Central ID:
    PMC6938228
  • Document Type:
  • Funding:
  • Volume:
    222
  • Issue:
    5
  • Collection(s):
  • Main Document Checksum:
    urn:sha256:8e8f8b074f2e5643d4e2187cbb715c2a1c4f1a804e2ca778d559ee5e068eda69
  • Download URL:
  • File Type:
    Filetype[PDF - 721.05 KB ]
File Language:
English
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