Enhanced study design for acute inhalation studies with hydrophobic surface-treated particles to determine toxicological effects including suffocation

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Gustav Gerd Bruer - , Fraunhofer Institute for Toxicology and Experimental Medicine (Author)
  • Otto Creutzenberg - , Fraunhofer Institute for Toxicology and Experimental Medicine (Author)
  • Paula Janssen - , Fraunhofer Institute for Toxicology and Experimental Medicine (Author)
  • Nils Krueger - , Evonik Operations GmbH (Author)
  • Jürgen Nolde - , Grace Europe Holding GmbH (Author)
  • Mehmet Ramazanoglu - , Fraunhofer Institute for Toxicology and Experimental Medicine (Author)
  • Dirk Schaudien - , Fraunhofer Institute for Toxicology and Experimental Medicine (Author)
  • Tobias B. Schuster - , Evonik Operations GmbH (Author)
  • Michael Stintz - (Author)
  • Nils Warfving - , AnaPath GmbH (Author)
  • Benno Wessely - , Mechanical Process Engineering Group (Author)
  • Klaus Weber - , AnaPath GmbH (Author)

Abstract

High concentrations of low-density particles may cause effects in acute inhalation toxicity studies which can be easily underestimated or misinterpreted following strictly the OECD TG 436, i.e., limited parameters as mortality and gross lesions will be evaluated only. Seven particle types (synthetic amorphous silica (SAS) HMDZ-SAS, silica gel, pyrogenic SAS, and precipitated SAS, calcium carbonate, aluminum oxide pyrogenic alumina, organic red pigment) were chosen at the highest technically feasible concentration of approximately 500 mg/m3 for acute inhalation studies with an expanded endpoint setup. Therefore additional parameters and a thorough histopathological evaluation of an extensive set of organs, including the respiratory tract emphasizing the nasal cavities were added. Six Crl:WI rats per study were exposed for four hours from which three animals were sacrificed after 24 hours and three animals after 14 days. HMDZ-SAS caused early death in all animals due to blockage of the nasal passages caused by its hydrophobicity. For all other Si-containing compounds, histology revealed minor inflammatory and reactive lesions in lungs after 24 hours that were still present after 14 days, except in silica gel-treated animals. After 14 days, for pyrogenic SAS, precipitated SAS, and pyrogenic alumina, granulomas formed in the BALT and lung-associated lymph nodes. In contrast, the calcium carbonate induced almost no findings, and the red pigment (also tested for the additional dose of 1000 mg/m3) stuck partially to the nasal mucosa without causing pathological damage and partly entered the lungs without showing any adverse effects. The results of the present study highlight the advantage of improving the rather simple study design of acute inhalation studies by implementing an extended study design.

Details

Original languageEnglish
Pages (from-to)31-48
Number of pages18
JournalToxicology Letters
Volume399
Issue numberSuppl. 1
Publication statusPublished - Aug 2024
Peer-reviewedYes

External IDs

Scopus 85189669070

Keywords