Markers of lipid oxidative damage in the exhaled breath condensate of nano TiO2 production workers
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
- Keywords
- Nanoparticles, TiO2, aldehydes, exhaled breath condensate, monitoring, occupational exposure, oxidative stress,
- MeSH
- Biomarkers analysis urine MeSH
- Chemical Industry MeSH
- Breath Tests MeSH
- Dinoprost analogs & derivatives analysis urine MeSH
- Humans MeSH
- Malondialdehyde analysis urine MeSH
- Lipid Metabolism MeSH
- Environmental Monitoring methods MeSH
- Nanoparticles analysis toxicity MeSH
- Oxidation-Reduction MeSH
- Oxidative Stress drug effects MeSH
- Lipid Peroxidation drug effects MeSH
- DNA Damage MeSH
- Occupational Exposure adverse effects analysis MeSH
- Spectrophotometry, Atomic MeSH
- Titanium analysis toxicity MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- 8-epi-prostaglandin F2alpha MeSH Browser
- Biomarkers MeSH
- Dinoprost MeSH
- Malondialdehyde MeSH
- Titanium MeSH
- titanium dioxide MeSH Browser
Nanoscale titanium dioxide (nanoTiO2) is a commercially important nanomaterial. Animal studies have documented lung injury and inflammation, oxidative stress, cytotoxicity and genotoxicity. Yet, human health data are scarce and quantitative risk assessments and biomonitoring of exposure are lacking. NanoTiO2 is classified by IARC as a group 2B, possible human carcinogen. In our earlier studies we documented an increase in markers of inflammation, as well as DNA and protein oxidative damage, in exhaled breath condensate (EBC) of workers exposed nanoTiO2. This study focuses on biomarkers of lipid oxidation. Several established lipid oxidative markers (malondialdehyde, 4-hydroxy-trans-hexenal, 4-hydroxy-trans-nonenal, 8-isoProstaglandin F2α and aldehydes C6-C12) were studied in EBC and urine of 34 workers and 45 comparable controls. The median particle number concentration in the production line ranged from 1.98 × 104 to 2.32 × 104 particles/cm3 with ∼80% of the particles <100 nm in diameter. Mass concentration varied between 0.40 and 0.65 mg/m3. All 11 markers of lipid oxidation were elevated in production workers relative to the controls (p < 0.001). A significant dose-dependent association was found between exposure to TiO2 and markers of lipid oxidation in the EBC. These markers were not elevated in the urine samples. Lipid oxidation in the EBC of workers exposed to (nano)TiO2 complements our earlier findings on DNA and protein damage. These results are consistent with the oxidative stress hypothesis and suggest lung injury at the molecular level. Further studies should focus on clinical markers of potential disease progression. EBC has reemerged as a sensitive technique for noninvasive monitoring of workers exposed to engineered nanoparticles.
b Institute of Chemical Process Fundamentals of the CAS Prague Czech Republic
c Institute of Chemical Technology Prague Prague Czech Republic
f J Heyrovský Institute of Physical Chemistry of the CAS Prague Czech Republic
h UMass Lowell Department of Public Health College of Health Sciences Lowell MA USA
References provided by Crossref.org
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