dc.contributor.author
Thoma, Tizia
dc.contributor.author
Ma-Hock, Lan
dc.contributor.author
Schneider, Steffen
dc.contributor.author
Honarvar, Naveed
dc.contributor.author
Treumann, Silke
dc.contributor.author
Groeters, Sibylle
dc.contributor.author
Strauss, Volker
dc.contributor.author
Marxfeld, Heike
dc.contributor.author
Funk-Weyer, Dorothee
dc.contributor.author
Landsiedel, Robert
dc.date.accessioned
2024-06-03T07:27:40Z
dc.date.available
2024-06-03T07:27:40Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/43725
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-43440
dc.description.abstract
Background
Significant variations exist in the forms of ZnO, making it impossible to test all forms in in vivo inhalation studies. Hence, grouping and read-across is a common approach under REACH to evaluate the toxicological profile of familiar substances. The objective of this paper is to investigate the potential role of dissolution, size, or coating in grouping ZnO (nano)forms for the purpose of hazard assessment. We performed a 90-day inhalation study (OECD test guideline no. (TG) 413) in rats combined with a reproduction/developmental (neuro)toxicity screening test (TG 421/424/426) with coated and uncoated ZnO nanoforms in comparison with microscale ZnO particles and soluble zinc sulfate. In addition, genotoxicity in the nasal cavity, lungs, liver, and bone marrow was examined via comet assay (TG 489) after 14-day inhalation exposure.
Results
ZnO nanoparticles caused local toxicity in the respiratory tract. Systemic effects that were not related to the local irritation were not observed. There was no indication of impaired fertility, developmental toxicity, or developmental neurotoxicity. No indication for genotoxicity of any of the test substances was observed. Local effects were similar across the different ZnO test substances and were reversible after the end of the exposure.
Conclusion
With exception of local toxicity, this study could not confirm the occasional findings in some of the previous studies regarding the above-mentioned toxicological endpoints. The two representative ZnO nanoforms and the microscale particles showed similar local effects. The ZnO nanoforms most likely exhibit their effects by zinc ions as no particles could be detected after the end of the exposure, and exposure to rapidly soluble zinc sulfate had similar effects. Obviously, material differences between the ZnO particles do not substantially alter their toxicokinetics and toxicodynamics. The grouping of ZnO nanoforms into a set of similar nanoforms is justified by these observations.
en
dc.format.extent
29 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Nanoparticles
en
dc.subject
Genotoxicity
en
dc.subject
Reproductive toxicity
en
dc.subject
Developmental toxicity
en
dc.subject
Inhalation toxicity
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik
dc.title
Toxicological inhalation studies in rats to substantiate grouping of zinc oxide nanoforms
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
24
dcterms.bibliographicCitation.doi
10.1186/s12989-024-00572-y
dcterms.bibliographicCitation.journaltitle
Particle and Fibre Toxicology
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.volume
21
dcterms.bibliographicCitation.url
https://doi.org/10.1186/s12989-024-00572-y
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Pharmazie
refubium.funding
Springer Nature DEAL
refubium.note.author
Die Publikation wurde aus Open Access Publikationsgeldern der Freien Universität Berlin gefördert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1743-8977