Pulmonary effects of different sized and oxidized forms of graphene nanoparticles
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2016/03/01
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Description:Risk of graphene (Gr) nanoparticle inhalation by workers during the manufacture of composite materials is a growing concern as new graphene nanomaterials are generated and utilized. Gr-induced cytotoxicity in vitro (PC12 cells, fibroblasts) and lung inflammation in vivo have been demonstrated, and Roberts et al (2013) showed that lung inflammation was increased up to 7 d after aspiration of non-oxidized Gr particles with lateral dimensions >5 microM and greater number of layers (approximately 20) compared with that of smaller particles (<1 microM, approximately 4 layers). We reported previously that a single exposure of graphene [5 microm lateral x 7-10 nm thick (Gr5)] transiently increased lung resistance (RL), dynamic lung compliance (CDyn) and reactivity to inhaled methacholine (MCh) in mice. In this study we examined the effects two additional sizes of non-oxidized Gr particles [20 microm lateral x 7-10 nm thick (Gr20), and <2 microm lateral x 1-2 nm thick (Gr1)] as well as a reduced form of oxidized Gr (rGO), on basal RL and CDyn and reactivity to inhaled methacholine (MCh). Mice were given 40 microg Gr (Gr1, Gr20 or rGO) suspended in dispersion medium (DM; control) via aspiration. Basal levels and RL and CDyn responses to increasing concentrations of inhaled MCh were measured 4 h - 2 mo after Gr exposure. Gr1 increased basal RL on day 7 and basal RL decreased at 2 mo. Gr1 increased Cdyn responses to MCh 1 mo post-exposure, which returned to control levels at 2 mo. However, basal Cdyn was increased by 2 mo post-exposure. Gr20 increased Cdyn responses to MCh 1 mo post-exposure, but Cdyn returned to control by 2 mo. rGO had no effect on basal RL or Cdyn, nor MCh reactivity. Our results indicate that exposure to non-oxidized Gr nanoparticles resulted in transient changes in RL or Cdyn responses to MCh, while the reduced form rGO had no significant effect on airway reactivity or basal RL or Cdyn. Basal Cdyn was increased 2 mo after exposure to Gr1. Our findings suggest that the pulmonary effects of graphenes are influenced by particle size, number of layers and oxidative/reduced state. [Description provided by NIOSH]
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ISSN:1096-6080
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Volume:150
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Issue:1
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NIOSHTIC Number:nn:20047821
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Citation:Toxicologist 2016 Mar; 150(1):584
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Federal Fiscal Year:2016
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Peer Reviewed:False
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Source Full Name:The Toxicologist. Society of Toxicology 55th Annual Meeting and ToxExpo, March 13-17, 2016, New Orleans, Louisiana
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Main Document Checksum:urn:sha-512:ef3e692c5018aacb99f36b5b1d7485f3e25f03ec4880fdbb5c0cd863b515d4dc4e05cfb0e58898acc38aef66e2a0d975c73a8355b420ad3f16e45a346aeb6127
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