Journal of Occupational and Environmental Medicine · 2011 · 64 citations · 58 references
Veterinary MedicineImmunologyToxicologyInflammationInnate ImmunityNanomaterialsInflammatory BiomarkersNanotoxicologyNanotubesPulmonary InflammationPulmonary ToxicityPulmonary ToxicologyAcute-phase MediatorsAcute-phase ProteinsBiomarkers Of Pulmonary InjuryCarbon Nanotube ToxicityEarly Tissue EffectsLung Inflammation BiomarkersPulmonary Toxicity BiomarkersSystemic Inflammation Markers
OBJECTIVE: Interest exists for early monitoring of worker exposure to engineered nanomaterials. Here, we highlight quantitative systemic markers of early effects after carbon nanotube (CNT) exposure. METHODS: Mice were exposed by pharyngeal aspiration to 40-μg CNT and harvested 24 hours, 7 days, and 28 days postexposure for measurements of whole blood, lung and extrapulmonary tissue gene expression, blood and bronchoalveolar lavage (BAL) differentials, and serum protein profiling. RESULTS: Early effects included increased inflammatory blood gene expression and serum cytokines followed by an acute phase response (eg, CRP, SAA-1, SAP). Beyond 24 hours, there was a consistent increase in blood and BAL eosinophils. At 28 day, serum acute phase proteins with immune function including complement C3, apolipoproteins A-I and A-II, and α₂-macroglobulin were increased. CONCLUSIONS: Carbon nanotube exposure resulted in measurable systemic markers but lacked specificity to distinguish from other pulmonary exposures.
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Respiratory toxicity of multi-wall carbon nanotubes
Julie Muller, François Huaux, Nicolas Moreau et al. · Toxicology and Applied Pharmacology · 2005 · 1.1K citations
Subodh Verma, Chao‐Hung Wang, Shuhong Li et al. · Circulation · 2002 · 1.1K citations