Suitability of Tedlar gas sampling bags for siloxane quantification in landfill gas.

Landfill or digester gas can contain man-made volatile methylsiloxanes (VMS), usually in the range of a few milligrams per normal cubic metre (Nm(3)). Until now, no standard method for siloxane quantification exists and there is controversy with respect to which sampling procedure is most suitable. This paper presents an analytical and a sampling procedure for the quantification of common VMS in biogas via GC-MS and polyvinyl fluoride (Tedlar) bags. Two commercially available Tedlar bag models are studied. One is equipped with a polypropylene valve with integrated septum, the other with a dual port fitting made from stainless steel. Siloxane recovery in landfill gas samples is investigated as a function of storage time, temperature, surface-to-volume ratio and background gas. Recovery was found to depend on the type of fitting employed. The siloxanes sampled in the bag with the polypropylene valve show high and stable recovery, even after more than 30 days. Sufficiently low detection limits below 10 microg Nm(-3) and good reproducibility can be achieved. The method is therefore well applicable to biogas, greatly facilitating sampling in comparison with other common techniques involving siloxane enrichment using sorption media.

Gene expression profiling of in vitro cultured macrophages after exposure to the respiratory sensitizer hexamethylene diisocyanate.

Occupational exposure to chemicals is one of the main causes of respiratory allergy and asthma. Identification of chemicals that trigger allergic asthma is difficult as underlying processes and specific markers have not yet been clearly defined. Moreover, adequate classification of the respiratory toxicity of chemicals is hampered due to the lack of validated in vivo and in vitro test methods. The study of differential gene expression profiles in appropriate human in vitro cell systems is a promising approach to identify selective markers for respiratory allergy. As alveolar macrophages display important immunological and inflammatory properties in response to foreign substances in the lung, we aimed at gaining more insight in changes of human macrophages transcriptome and to identify selective genetic markers for respiratory sensitization in response to hexamethylene diisocyanate (HDI). In vitro cultures of human THP-1 cells were differentiated into macrophages and exposed to 55 microg/ml HDI for 6 and 10h. Using human oligonucleotide microarrays, changes were observed in the expression of genes that are involved in diverse biological and molecular processes, including detoxification, oxidative stress, cytokine signaling, and apoptosis, which can lead to the development of asthma. These genes are possible markers for respiratory sensitization caused by isocyanates.