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Quantitative biokinetics over a 28day period of freshly generated, pristine, 20 nm titanium dioxide nanoparticle aerosols in healthy adult rats after a single two-hour inhalation exposure.
Part. Fibre Toxicol. 16:29 (2019)
BackgroundIndustrially produced quantities of TiO2 nanoparticles are steadily rising, leading to an increasing risk of inhalation exposure for both professionals and consumers. Particle inhalation can result in inflammatory and allergic responses, and there are concerns about other negative health effects from either acute or chronic low-dose exposure.ResultsTo study the fate of inhaled TiO2-NP, adult rats were exposed to 2-h intra-tracheal inhalations of V-48-radiolabeled, 20nm TiO2-NP aerosols (deposited NP-mass 1.40.5 mu g). At five time points (1h, 4h, 24h, 7d, 28d) post-exposure, a complete balance of the [V-48]TiO2-NP fate was quantified in organs, tissues, carcass, lavage and body fluids, including excretions.After fast mucociliary airway clearance (fractional range 0.16-0.31), long-term macrophage-mediated clearance (LT-MC) from the alveolar region is 2.6-fold higher after 28d (integral fraction 0.40 +/- 0.04) than translocation across the air-blood-barrier (integral fraction 0.15 +/- 0.01). A high NP fraction remains in the alveoli (0.44 +/- 0.05 after 28d), half of these on the alveolar epithelium and half in interstitial spaces. There is clearance from both retention sites at fractional rates (0.02-0.03 d(-1)) by LT-MC. Prior to LT-MC, [V-48]TiO2-NP are re-entrained to the epithelium as reported earlier for 20nm inhaled gold-NP (AuNP) and iridium-NP (IrNP).Conclusion Comparing the 28-day biokinetics patterns of three different inhaled NP materials TiO2-NP, AuNP and IrNP, the long-term kinetics of interstitial relocation and subsequent re-entrainment onto the lung-epithelium is similar for AuNP and Ir-NP but slower than for TiO2-NP. We discuss mechanisms and pathways of NP relocation and re-entrainment versus translocation. Additionally, after 28days the integral translocated fractions of TiO2-NP and IrNP across the air-blood-barrier (ABB) are similar and become 0.15 while the translocated AuNP fraction is only 0.04. While NP dissolution proved negligible, translocated TiO2-NP and IrNP are predominantly excreted in urine (0.1) while the urinary AuNP excretion amounts to a fraction of only 0.01. Urinary AuNP excretion is below 0.0001 during the first week but rises tenfold thereafter suggesting delayed disagglomeration. Of note, all three NP dissolve minimally, since no ionic radio-label release was detectable. These biokinetics data of inhaled, same-sized NP suggest significant time-dependent differences of the ABB translocation and subsequent fate in the organism.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Spark Ignition Generated Titanium Dioxide Nanoparticle Aerosols ; Characterization Of Physicochemical Particle Properties ; Intratracheal Inhalation Of Freshly Generated Aerosols ; Translocation Across Air-blood-barrier ; Accumulation In Secondary Organs And Tissues ; Long-term Alveolar Macrophage-mediated Nanoparticle Clearance ; Nanoparticle Relocation Into The Interstitium ; Re-entrainment From Interstitium Back To Lung Epithelium For Clearance Towards The Larynx; Pulmonary Macrophagic System; Insoluble Iridium Particles; Intratracheal Instillation; Interstitial Macrophages; Extrapulmonary Organs; Alveolar Macrophage; Ultrafine Particles; Protein Corona; Lung; Clearance
Language
english
Publication Year
2019
HGF-reported in Year
2019
ISSN (print) / ISBN
1743-8977
e-ISSN
1743-8977
Journal
Particle and Fibre Toxicology
Quellenangaben
Volume: 16,
Issue: 1,
Article Number: 29
Publisher
Bmc
Publishing Place
London
Reviewing status
Peer reviewed
Institute(s)
Institute of Epidemiology (EPI)
Institute of Lung Health and Immunity (LHI)
Institute of Lung Health and Immunity (LHI)
POF-Topic(s)
30202 - Environmental Health
Research field(s)
Genetics and Epidemiology
Lung Research
Lung Research
PSP Element(s)
G-504000-010
G-505000-001
G-501600-006
G-505000-001
G-501600-006
WOS ID
WOS:000475558100001
Scopus ID
85069164528
PubMed ID
31288843
Erfassungsdatum
2019-07-22