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Details

Autor(en) / Beteiligte
Titel
Particle size dependent deposition and pulmonary inflammation after short-term inhalation of silver nanoparticles
Ist Teil von
  • Particle and fibre toxicology, 2014-09, Vol.11 (1), p.49-49, Article 49
Ort / Verlag
England: BioMed Central Ltd
Erscheinungsjahr
2014
Link zum Volltext
Quelle
Free E-Journal (出版社公開部分のみ)
Beschreibungen/Notizen
  • Although silver nanoparticles are currently used in more than 400 consumer products, it is not clear to what extent they induce adverse effects after inhalation during production and use. In this study, we determined the lung burden, tissue distribution, and the induction and recovery of adverse effects after short-term inhalation exposure to 15 nm and 410 nm silver nanoparticles. Rats were nose-only exposed to clean air, 15 nm silver nanoparticles (179 μg/m³) or 410 nm silver particles (167 μg/m³) 6 hours per day, for four consecutive days. Tissue distribution and the induction of pulmonary toxicity were determined at 24 hours and 7 days after exposure and compared with the internal alveolar dose. Presence of silver nanoparticles in lung cells was visualized by transmission electron microscopy (TEM). Exposure to 15 nm silver nanoparticles induced moderate pulmonary toxicity compared to the controls, indicated by a 175-fold increased influx of neutrophils in the lungs, a doubling of cellular damage markers in the lungs, a 5-fold increase in pro-inflammatory cytokines, and a 1.5-fold increase in total glutathione at 24 hours after exposure. All the observed effects disappeared at 7 days after exposure. No effects were observed after exposure to 410 nm silver particles. The internal alveolar mass dose of the 15 nm nanoparticles was 3.5 times higher compared to the 410 nm particles, which equals to a 66,000 times higher particle number. TEM analysis revealed 15 nm nanoparticles in vesicles and nuclei of lung cells, which were decreased in size to <5 nm at 24 hours after exposure. This demonstrates substantial dissolution of the silver nanoparticles. The results show a clear size-dependent effect after inhalation of similar mass concentrations of 15 nm and 410 nm silver (nano)particles. This can be partially explained by the difference in the internal alveolar dose between the 15 nm and 410 nm silver (nano)particles as well as by a difference in the release rate of silver ions.
Sprache
Englisch
Identifikatoren
ISSN: 1743-8977
eISSN: 1743-8977
DOI: 10.1186/s12989-014-0049-1
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4410796
Format
Schlagworte
Air Pollutants - analysis, Air Pollutants - chemistry, Air Pollutants - toxicity, Animals, Antimicrobial agents, Atoms & subatomic particles, Biomarkers - metabolism, Cell Nucleus - chemistry, Cell Nucleus - drug effects, Cell Nucleus - immunology, Cell Nucleus - ultrastructure, Confidence intervals, Cytokines, Cytokines - agonists, Cytokines - metabolism, Cytoplasmic Vesicles - chemistry, Cytoplasmic Vesicles - drug effects, Cytoplasmic Vesicles - immunology, Cytoplasmic Vesicles - ultrastructure, Glutathione - agonists, Glutathione - metabolism, Health aspects, Inhalation Exposure - adverse effects, Lung - chemistry, Lung - drug effects, Lung - immunology, Lung - ultrastructure, Lungs, Male, Metal Nanoparticles - administration & dosage, Metal Nanoparticles - analysis, Metal Nanoparticles - chemistry, Metal Nanoparticles - toxicity, Microscopy, Nanomaterials, Nanoparticles, Nanotechnology, Neutrophil Infiltration - drug effects, Oxidative stress, Particle Size, Pneumonia - chemically induced, Pneumonia - immunology, Pneumonia - metabolism, Pneumonia - pathology, Public health, Random Allocation, Rats, Inbred F344, Respiratory Mucosa - chemistry, Respiratory Mucosa - drug effects, Respiratory Mucosa - immunology, Respiratory Mucosa - ultrastructure, Respiratory Tract Absorption, Risk assessment, Silver, Silver - administration & dosage, Silver - analysis, Silver - chemistry, Silver - toxicity, Specific Pathogen-Free Organisms, Standard deviation, Studies, Tissue Distribution, Toxicity, Toxicity Tests, Acute, Toxicokinetics

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