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Analytical in vitro approach for studying cyto- and genotoxic effects of particulate airborne material

Identifieur interne : 002324 ( Main/Exploration ); précédent : 002323; suivant : 002325

Analytical in vitro approach for studying cyto- and genotoxic effects of particulate airborne material

Auteurs : Michaela Aufderheide [Allemagne] ; Stefanie Scheffler [Allemagne] ; Niklas Möhle [Allemagne] ; Beat Halter [Suisse] ; Dieter Hochrainer [Allemagne]

Source :

RBID : ISTEX:20BBAA8D8F5D097A4ABAB87A1912183C25216AD5

English descriptors

Abstract

Abstract: In the field of inhalation toxicology, progress in the development of in vitro methods and efficient exposure strategies now offers the implementation of cellular-based systems. These can be used to analyze the hazardous potency of airborne substances like gases, particles, and complex mixtures (combustion products). In addition, the regulatory authorities require the integration of such approaches to reduce or replace animal experiments. Although the animal experiment currently still has to provide the last proof of the toxicological potency and classification of a certain compound, in vitro testing is gaining more and more importance in toxicological considerations. This paper gives a brief characterization of the CULTEX® Radial Flow System exposure device, which allows the exposure of cultivated cells as well as bacteria under reproducible and stable conditions for studying cellular and genotoxic effects after the exposure at the air–liquid or air–agar interface, respectively. A commercial bronchial epithelial cell line (16HBE14o-) as well as Salmonella typhimurium tester strains were exposed to smoke of different research and commercial available cigarettes. A dose-dependent reduction of cell viability was found in the case of 16HBE14o- cells; S. typhimurium responded with a dose-dependent induction of revertants. The promising results recommend the integration of cellular studies in the field of inhalation toxicology and their regulatory acceptance by advancing appropriate validation studies.

Url:
DOI: 10.1007/s00216-011-5163-4


Affiliations:


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