In Vitro Cytoxicity profile of E-Cigarette Liquid Samples on Primary Human Bronchial Epithelial Cells”

Did you encounter a typo?

We are human, after all.

Contact us now and we will arrange it as soon as possible

Acknowledging CoEHAR in your work

If CoEHAR training and education, events, resources, equipment or staff have helped your project, we appreciate an acknowledgement in your papers, articles, presentations, posters, blog post with a citation and/ or link. It helps us to spread the word about our services and demonstrate our ongoing value to our Funders.

If you wish to cite CoEHAR in a research paper or presentation, use the following sample text:

We wish to thank the Center of Excellence for the Acceleration of Harm Reduction (CoEHAR, University of Catania, Italy- COE01-05) for assisting our project with the resources provided.

Massimo Caruso, Alfio Distefano, Rosalia Emma, Pietro Zuccarello, Chiara Copat, Margherita Ferrante, Giuseppe Carota, Roberta Pulvirenti, Riccardo Polosa, Gesualdo Antonio Missale, Sonja Rust, Giuseppina Raciti, Giovanni Li Volti

Abstract

Cigarette smoke is associated to severe chronic diseases. The most harmful components of cigarette smoke derive from the combustion process, which are significantly reduced in the electronic cigarette aerosol, thus providing a valid option in harm reduction strategies. To develop safer products, it is therefore necessary to screen electronic cigarette liquids (e-liquids) to meet high safety standards defined by government regulations. The aim of the present study was to evaluate the presence of metal- and plastic-derived contaminants in four different commercial e-liquids with high concentration of nicotine and their cytotoxic effect in normal human bronchial epithelial cells by a number of in vitro assays, in comparison with the 1R6F reference cigarette, using an air-liquid interface (ALI) exposure system. Moreover, we evaluated the effect of aerosol exposure on oxidative stress by measuring the production of reactive oxygen species and mitochondrial potential. Our results showed no contaminants in all e-liquids and a significantly reduced cytotoxic effect of e-liquid aerosol compared to cigarette smoke as well as a maintained mitochondria integrity. Moreover, no production of reactive oxygen species was detected with e-cigarette aerosol. In conclusion, these results support the reduced toxicity potential of e-cigs compared to tobacco cigarettes in an in vitro model resembling real life smoke exposure.