Characterisation of a Vitrocell® VC 10 in vitrosmoke exposure system using dose tools and biological analysis

• Published in: Chemistry Central journal 2013-09, Vol.7 (1), Article 146
• Main Authors: Thorne, David, Kilford, Joanne, Payne, Rebecca, Adamson, Jason, Scott, Ken, Dalrymple, Annette, Meredith, Clive, Dillon, Deborah
• Format: Article
• Language: English
• Subjects: Chemistry; Chemistry and Materials Science; Chemistry/Food Science; Environmental and Energy Chemistry; Research Article
• ISSN: 1752-153X; 1752-153X
• DOI: 10.1186/1752-153X-7-146

Background The development of whole smoke exposure systems have been driven by the fact that traditional smoke exposure techniques are based on the particulate phase of tobacco smoke and not the complete smoke aerosol. To overcome these challenges in this study, we used a Vitrocell® VC 10 whole smoke exposure system. For characterisation purposes, we determined smoke deposition in relationship to airflow (L/min), regional smoke deposition within the linear exposure module, vapour phase dilution using a known smoke marker (carbon monoxide) and finally assessed biological responses using two independent biological systems, the Ames and Neutral Red uptake (NRU) assay. Results Smoke dilution correlates with particulate deposition (R 2  = 0.97) and CO concentration (R 2  = 0.98). Regional deposition analysis within the linear exposure chamber showed no statistical difference in deposited mass across the chamber at any airflows tested. Biological analysis showed consistent responses and positive correlations with deposited mass for both the Ames (R 2  = 0.76) and NRU (R 2  = 0.84) assays. Conclusions We conclude that in our study, under the experimental conditions tested, the VC 10 can produce stable tobacco smoke dilutions, as demonstrated by particulate deposition, measured vapour phase smoke marker delivery and biological responses from two independent in vitro test systems.