4.7 Article

Hazard assessment of abraded thermoplastic composites reinforced with reduced graphene oxide

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 435, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2022.129053

Keywords

Graphene-related materials; Thermoplastic polymer composites; Hazard assessment

Funding

  1. European Union (EU) [785219, 881603]
  2. University of Trieste
  3. Agence Nationale de la Recherche (ANR) through the LabEx project Chemistry of Complex Systems [ANR-10-LABX-0026_CSC]
  4. Maria de Maeztu Units of Excellence Program from the Spanish State Research Agency [MDM-2017-0720]
  5. Swiss National Science Foundation [310030_169207]
  6. UKRI Biotechnology and Biological Sciences Research Council (UKRI-BBSRC)
  7. Wellcome Trust
  8. University of Manchester Strategic Fund
  9. Swiss National Science Foundation (SNF) [310030_169207] Funding Source: Swiss National Science Foundation (SNF)

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This study conducted a comprehensive investigation on the potential biological effects of particles released from graphene-reinforced composites. The results showed that exposure to PA6-rGO induced mild and transient pulmonary inflammation, while exposure to rGO induced longer-lasting moderate inflammation. Overall, the study suggests a negligible impact on human health under acute exposure conditions of graphene-related materials.
Graphene-related materials (GRMs) are subject to intensive investigations and considerable progress has been made in recent years in terms of safety assessment. However, limited information is available concerning the hazard potential of GRM-containing products such as graphene-reinforced composites. In the present study, we conducted a comprehensive investigation of the potential biological effects of particles released through an abrasion process from reduced graphene oxide (rGO)-reinforced composites of polyamide 6 (PA6), a widely used engineered thermoplastic polymer, in comparison to as-produced rGO. First, a panel of well-established in vitro models, representative of the immune system and possible target organs such as the lungs, the gut, and the skin, was applied. Limited responses to PA6-rGO exposure were found in the different in vitro models. Only asproduced rGO induced substantial adverse effects, in particular in macrophages. Since inhalation of airborne materials is a key occupational concern, we then sought to test whether the in vitro responses noted for these materials would translate into adverse effects in vivo. To this end, the response at 1, 7 and 28 days after a single pulmonary exposure was evaluated in mice. In agreement with the in vitro data, PA6-rGO induced a modest and transient pulmonary inflammation, resolved by day 28. In contrast, rGO induced a longer-lasting, albeit moderate inflammation that did not lead to tissue remodeling within 28 days. Taken together, the present study suggests a negligible impact on human health under acute exposure conditions of GRM fillers such as rGO when released from composites at doses expected at the workplace.

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