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Drinking water (DW) quality can change during distribution, leading to taste and odor events and microbial regrowth. Pilot plants mimicking distribution networks are crucial for understanding these changes. We present a new pilot plant design, including piping material, sensors, and instrumentation. The three independent loops (100 m each) of the pilot exhibit identical behavior, allowing simultaneous testing of three conditions. Monitoring includes taste and odor compound formation, microorganism regrowth, and dissolved organic carbon changes. Real-time measurements enable continuous monitoring, and inner pipe biofilm sampling is feasible. The pilot's modularity facilitates studying climate change effects, different piping materials, and source waters on DW quality in the distribution network. [ABSTRACT FROM AUTHOR]

Introduction: Malignant pleural mesothelioma (MPM) is a lethal cancer for which early-stage diagnosis remains a major challenge. Volatile organic compounds (VOCs) in breath proved to be potential biomarkers for MPM diagnosis, but translational studies are needed to elucidate which VOCs originate from the tumor itself and thus are specifically related to MPM cell metabolism. Methods: An in vitro model was set-up to characterize the headspace VOC profiles of six MPM and two lung cancer cell lines using thermal desorption-gas chromatography-mass spectrometry. A comparative analysis was carried out to identify VOCs that could discriminate between MPM and lung cancer, as well as between the histological subtypes within MPM (epithelioid, sarcomatoid and biphasic). Results: VOC profiles were identified capable of distinguishing MPM (subtypes) and lung cancer cells with high accuracy. Alkanes, aldehydes, ketones and alcohols represented many of the discriminating VOCs. Discrepancies with clinical findings were observed, supporting the need for studies examining breath and tumor cells of the same patients and studying metabolization and kinetics of in vitro discovered VOCs in a clinical setting. Conclusion: While the relationship between in vitro and in vivo VOCs is yet to be established, both could complement each other in generating a clinically useful breath model for MPM. [ABSTRACT FROM AUTHOR]