September 13-16, 2009
K. Sewald, S. Switalla, D. Ritter, N. Krug, J. Knebel, A. Braun
Fraunhofer Institute for Toxicology and Environmental Medicine, Hannover, Germany
Precise cut lung slices were washed and exposed to synthetic air, O3 and NO2 in an air-liquid interface. Viability was controlled by Wst-1 and LIVE/DEAD® staining. Cytokines were quantified by ELISA or Luminex technology.
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