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Published on: August 25, 2018
In utero exposure to electronic cigarette carriers alters craniofacial morphology
Ethan Richlak1,2, Logan Shope3, Ethan Leonard3
1Nationwide Children's Hospital Cleft Lip and Palate Center, Columbus, Ohio, United States of America.
A 30/70 propylene glycol/vegetable glycerin (PG/VG) electronic nicotine delivery system (ENDS) formulation significantly reduced craniofacial growth in mice. This suggests that even nicotine-free ENDS may pose risks, particularly for pregnant populations.
Area of Science:
- Toxicology
- Developmental Biology
- Public Health
Background:
- Electronic nicotine delivery systems (ENDS) are popular, but e-liquid formulations lack consistent regulation.
- Common e-liquids contain propylene glycol (PG) and vegetable glycerin (VG); higher VG content is often chosen to reduce potential harm.
- Previous research linked PG-based e-liquids to increased carcinogens and nicotine uptake.
Purpose of the Study:
- To investigate the impact of different PG/VG ratios on craniofacial development in the absence of nicotine.
- To test the hypothesis that a 30/70 PG/VG formulation is safer than a 50/50 PG/VG formulation regarding craniofacial growth.
Main Methods:
- In utero exposure of mouse litters to control (free air), 30/70 PG/VG, or 50/50 PG/VG e-liquid components.
- Assessment of skull morphology in pups at postnatal day 14.
Main Results:
- The 30/70 PG/VG exposed group showed significant reductions in body weight, facial, and cranial dimensions.
- No significant differences in craniofacial growth were observed between the control and 50/50 PG/VG groups.
Conclusions:
- A shift towards VG-centric e-liquid formulations (30/70 PG/VG) may not mitigate health concerns associated with ENDS use.
- Propylene glycol and vegetable glycerin are not inert carriers and may pose risks.
- Nicotine-free ENDS formulations, particularly those with higher VG content, may not be safe for use during pregnancy.
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