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Characterization of the Vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke

BACKGROUND: Only a few exposure systems are presently available that enable cigarette smoke exposure of living cells at the air–liquid interface, of which one of the most versatile is the Vitrocell® system (Vitrocell® Systems GmbH). To assess its performance and optimize the exposure conditions, we...

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Autores principales: Majeed, Shoaib, Frentzel, Stefan, Wagner, Sandra, Kuehn, Diana, Leroy, Patrice, Guy, Philippe A, Knorr, Arno, Hoeng, Julia, Peitsch, Manuel C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236458/
https://www.ncbi.nlm.nih.gov/pubmed/25411580
http://dx.doi.org/10.1186/s13065-014-0062-3
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author Majeed, Shoaib
Frentzel, Stefan
Wagner, Sandra
Kuehn, Diana
Leroy, Patrice
Guy, Philippe A
Knorr, Arno
Hoeng, Julia
Peitsch, Manuel C
author_facet Majeed, Shoaib
Frentzel, Stefan
Wagner, Sandra
Kuehn, Diana
Leroy, Patrice
Guy, Philippe A
Knorr, Arno
Hoeng, Julia
Peitsch, Manuel C
author_sort Majeed, Shoaib
collection PubMed
description BACKGROUND: Only a few exposure systems are presently available that enable cigarette smoke exposure of living cells at the air–liquid interface, of which one of the most versatile is the Vitrocell® system (Vitrocell® Systems GmbH). To assess its performance and optimize the exposure conditions, we characterized a Vitrocell® 24/48 system connected to a 30-port carousel smoking machine. The Vitrocell® 24/48 system allows for simultaneous exposure of 48 cell culture inserts using dilution airflow rates of 0–3.0 L/min and exposes six inserts per dilution. These flow rates represent cigarette smoke concentrations of 7–100%. RESULTS: By characterizing the exposure inside the Vitrocell® 24/48, we verified that (I) the cigarette smoke aerosol distribution is uniform across all inserts, (II) the utility of Vitrocell® crystal quartz microbalances for determining the online deposition of particle mass on the inserts, and (III) the amount of particles deposited per surface area and the amounts of trapped carbonyls and nicotine were concentration dependent. At a fixed dilution airflow of 0.5 L/min, the results showed a coefficient of variation of 12.2% between inserts of the Vitrocell® 24/48 module, excluding variations caused by different runs. Although nicotine and carbonyl concentrations were linear over the tested dilution range, particle mass deposition increased nonlinearly. The observed effect on cell viability was well-correlated with increasing concentration of cigarette smoke. CONCLUSIONS: Overall, the obtained results highlight the suitability of the Vitrocell® 24/48 system to assess the effect of cigarette smoke on cells under air–liquid interface exposure conditions, which is closely related to the conditions occurring in human airways.
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spelling pubmed-42364582014-11-19 Characterization of the Vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke Majeed, Shoaib Frentzel, Stefan Wagner, Sandra Kuehn, Diana Leroy, Patrice Guy, Philippe A Knorr, Arno Hoeng, Julia Peitsch, Manuel C Chem Cent J Research Article BACKGROUND: Only a few exposure systems are presently available that enable cigarette smoke exposure of living cells at the air–liquid interface, of which one of the most versatile is the Vitrocell® system (Vitrocell® Systems GmbH). To assess its performance and optimize the exposure conditions, we characterized a Vitrocell® 24/48 system connected to a 30-port carousel smoking machine. The Vitrocell® 24/48 system allows for simultaneous exposure of 48 cell culture inserts using dilution airflow rates of 0–3.0 L/min and exposes six inserts per dilution. These flow rates represent cigarette smoke concentrations of 7–100%. RESULTS: By characterizing the exposure inside the Vitrocell® 24/48, we verified that (I) the cigarette smoke aerosol distribution is uniform across all inserts, (II) the utility of Vitrocell® crystal quartz microbalances for determining the online deposition of particle mass on the inserts, and (III) the amount of particles deposited per surface area and the amounts of trapped carbonyls and nicotine were concentration dependent. At a fixed dilution airflow of 0.5 L/min, the results showed a coefficient of variation of 12.2% between inserts of the Vitrocell® 24/48 module, excluding variations caused by different runs. Although nicotine and carbonyl concentrations were linear over the tested dilution range, particle mass deposition increased nonlinearly. The observed effect on cell viability was well-correlated with increasing concentration of cigarette smoke. CONCLUSIONS: Overall, the obtained results highlight the suitability of the Vitrocell® 24/48 system to assess the effect of cigarette smoke on cells under air–liquid interface exposure conditions, which is closely related to the conditions occurring in human airways. Springer International Publishing 2014-11-12 /pmc/articles/PMC4236458/ /pubmed/25411580 http://dx.doi.org/10.1186/s13065-014-0062-3 Text en © Majeed et al.; licensee Chemistry Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Majeed, Shoaib
Frentzel, Stefan
Wagner, Sandra
Kuehn, Diana
Leroy, Patrice
Guy, Philippe A
Knorr, Arno
Hoeng, Julia
Peitsch, Manuel C
Characterization of the Vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke
title Characterization of the Vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke
title_full Characterization of the Vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke
title_fullStr Characterization of the Vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke
title_full_unstemmed Characterization of the Vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke
title_short Characterization of the Vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke
title_sort characterization of the vitrocell® 24/48 in vitro aerosol exposure system using mainstream cigarette smoke
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236458/
https://www.ncbi.nlm.nih.gov/pubmed/25411580
http://dx.doi.org/10.1186/s13065-014-0062-3
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