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Guemperlein, I.; Fischer, E.; Dietrich-Guemperlein, G.; Karrasch, Stefan ORCID logoORCID: https://orcid.org/0000-0001-9807-2915; Nowak, Dennis ORCID logoORCID: https://orcid.org/0000-0001-7871-8686; Jörres, Rudolf A. ORCID logoORCID: https://orcid.org/0000-0002-9782-1117 und Schierl, R. (2018): Acute health effects of desktop 3D printing (fused deposition modeling) using acrylonitrile butadiene styrene and polylactic acid materials: An experimental exposure study in human volunteers. In: Indoor Air, Bd. 28, Nr. 4: S. 611-623

Volltext auf 'Open Access LMU' nicht verfügbar.

Abstract

3D printers are increasingly run at home. Nanoparticle emissions from those printers have been reported, which raises the question whether adverse health effects from ultrafine particles (UFP) can be elicited by 3D printers. We exposed 26 healthy adults in a single-blinded, randomized, cross-over design to emissions of a desktop 3D printer using fused deposition modeling (FDM) for 1hour (high UFP-emitting acrylonitrile butadiene styrene [ABS] vs low-emitting polylactic acid [PLA]). Before and after exposures, cytokines (IL-1 beta, IL-6, TNF-alpha, INF-gamma) and ECP in nasal secretions, exhaled nitric oxide (FeNO), urinary 8-isoprostaglandin F-2 alpha (8-iso PGF(2 alpha)), and self-reported symptoms were assessed. The exposures had no significant differential effect on 8-iso PGF(2 alpha) and nasal biomarkers. However, there was a difference (P<.05) in the time course of FeNO, with higher levels after ABS exposure. Moreover, indisposition and odor nuisance were increased for ABS exposure. These data suggest that 1hour of exposure to 3D printer emissions had no acute effect on inflammatory markers in nasal secretions and urine. The slight relative increase in FeNO after ABS printing compared to PLA might be due to eosinophilic inflammation from inhaled UFP particles. This possibility should be investigated in further studies using additional biomarkers and longer observation periods.

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