A life cycle approach to engineered nanomaterial toxicity to provide context to potential health effects
Public Domain
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2017/03/01
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Details
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Personal Author:Afshari A ; Battelli L ; Birch, M. Eileen ; Bishop L ; Bunker K ; Casuccio G ; Cena L ; Dahm, Matthew M. ; Erdely A ; Evans DE ; Eye T ; Geraci, Charles L. ; Kang J ; Kashon ML ; Kodali V ; Lowry DT ; Mercer RR ; Mitchell CA ; Orandle M ; Sager T ; Sargent LM ; Schubauer-Berigan, Mary K. ; Schwegler-Berry D ; Siegrist KJ ; Stefaniak, Aleksandr B. ; Yanamala N ; Zeidler-Erdely PC ; Afshari A ; Battelli L ; Birch, M. Eileen ; Bishop L ; Bunker K ; Casuccio G ; Cena L ; Dahm, Matthew M. ; Erdely A ; Evans DE ; Eye T ; Geraci, Charles L. ; Kang J ; Kashon ML ; Kodali V ; Lowry DT ; Mercer RR ; Mitchell CA ; Orandle M ; Sager T ; Sargent LM ; Schubauer-Berigan, Mary K. ; Schwegler-Berry D ; Siegrist KJ ; Stefaniak, Aleksandr B. ; Yanamala N ; Zeidler-Erdely PC
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Description:Pulmonary toxicity studies primarily focus on as-produced engineered nanomaterials and rarely are guided by a life cycle perspective or integration with exposure assessment. Understanding toxicity beyond the as-produced (AP) material is critical, due to modifications needed to overcome barriers to commercialization of applications. We evaluated the toxicity of AP multi-walled carbon nanotubes (MWCNT: 16 nm diameter, 1-2 microm length), their polymer-coated (PC) counterparts (polyurethane or a proprietary poly(arylene ethynylene)), and the respirable aerosols generated from sanding (fine, P320) the PC nanotube-embedded or neat composites from two separate companies. Polymer coating minimizes the percent MWCNT incorporation into the composite, permits ease in handling, and can decrease dustiness thereby reducing potential inhalation exposures downstream. Male C57BL/6J mice exposed by oropharyngeal aspiration to 4 or 40 microg were harvested 1, 7, 28, and 84 d post-exposure. Using workplace exposure assessment to guide in vivo study design (e.g. deposited dose and material preparations to emulate personal breathing zone collections), dose- and time-dependent measures of pulmonary cytotoxicity, inflammation, and histopathology were expectedly observed for the AP MWCNT. Polymer coating the MWCNT did not enhance the pulmonary toxicity of AP nanotubes and toxicity was significantly attenuated with one coating. The aerosols generated from sanding composites embedded with PC nanotubes (0.15-3% by weight) contained no evidence of free nanotubes, and were primarily micron-sized particles with some MWCNT protrusions. Following pulmonary exposure, if the percent weight incorporation of PC nanotubes and composite matrix utilized altered particle size distribution, acute in vivo toxicity was affected, and if unaltered, toxicity was not different. Our study provides perspective that while the number of workers and consumers increases along the life cycle, toxicity and/or potential for exposure to the as-produced material may greatly diminish. [Description provided by NIOSH]
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ISSN:1096-6080
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Division:HELD - Health Effects Laboratory Division ; DSHEFS - Division of Surveillance, Hazard Evaluations, and Field Studies ; DART - Division of Applied Research and Technology ; RHD - Respiratory Health Division ; EID - Education and Information Division ; HELD - Health Effects Laboratory Division ; DSHEFS - Division of Surveillance, Hazard Evaluations, and Field Studies ; DART - Division of Applied Research and Technology ; RHD - Respiratory Health Division ; EID - Education and Information Division
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Volume:156
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Issue:1
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NIOSHTIC Number:nn:20049488
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Citation:Toxicologist 2017 Mar; 156(1):448
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Federal Fiscal Year:2017
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Peer Reviewed:False
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Source Full Name:The Toxicologist. Society of Toxicology 56th Annual Meeting and ToxExpo, March 12-16, 2017, Baltimore, Maryland
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Main Document Checksum:urn:sha-512:b6600c168c5f98c53834695d64c7978f2fdf0d412600edee53fccc01b5faff0a1b02a9dcd1ec3dc635b0fcc6f69997f101df6dbc575621ae8bff7986deee9612
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