Sayers Brian C, Germolec Dori R, Walker Nigel J, Shipkowski Kelly A, Stout Matthew D, Cesta Mark F, Roycroft Joseph H, White Kimber L, Baker Gregory L, Dill Jeffrey A, Smith Matthew J
a Division of the National Toxicology Program , National Institute of Environmental Health Sciences , Research Triangle Park , NC , USA.
b Department of Pharmacology and Toxicology , Virginia Commonwealth University , Richmond , VA , USA.
Nanotoxicology. 2016 Dec;10(10):1458-1468. doi: 10.1080/17435390.2016.1235737. Epub 2016 Sep 30.
C60 fullerene (C60), or buckminsterfullerene, is a spherical arrangement of 60 carbon atoms, having a diameter of approximately 1 nm, and is produced naturally as a by-product of combustion. Due to its small size, C60 has attracted much attention for use in a variety of applications; however, insufficient information is available regarding its toxicological effects. The effects on respiratory toxicity and immunotoxicity of C60 aggregates (50 nm [nano-C60] and 1 μm [micro-C60] diameter) were examined in B6C3F1/N mice and Wistar Han rats after nose-only inhalation for 13 weeks. Exposure concentrations were selected to allow for data evaluations using both mass-based and particle surface area-based exposure metrics. Nano-C60 exposure levels selected were 0.5 and 2 mg/m (0.033 and 0.112 m/m), while micro-C60 exposures were 2, 15 and 30 mg/m (0.011, 0.084 and 0.167 m/m). There were no systemic effects on innate, cell-mediated, or humoral immune function. Pulmonary inflammatory responses (histiocytic infiltration, macrophage pigmentation, chronic inflammation) were concentration-dependent and corresponded to increases in monocyte chemoattractant protein (MCP)-1 (rats) and macrophage inflammatory protein (MIP)-1α (mice) in bronchoalveolar lavage (BAL) fluid. Lung overload may have contributed to the pulmonary inflammatory responses observed following nano-C60 exposure at 2 mg/m and micro-C60 exposure at 30 mg/m. Phenotype shifts in cells recovered from the BAL were also observed in all C60-exposed rats, regardless of the level of exposure. Overall, more severe pulmonary effects were observed for nano-C60 than for micro-C60 for mass-based exposure comparisons. However, for surface-area-based exposures, more severe pulmonary effects were observed for micro-C60 than for nano-C60, highlighting the importance of dosimetry when evaluating toxicity between nano- and microparticles.
C60富勒烯(C60),即巴基球,是由60个碳原子组成的球形结构,直径约为1纳米,是燃烧的天然副产品。由于其尺寸小,C60在各种应用中备受关注;然而,关于其毒理学效应的信息却不足。在B6C3F1/N小鼠和Wistar Han大鼠经鼻吸入13周后,研究了C60聚集体(直径50纳米[nano-C60]和1微米[micro-C60])对呼吸毒性和免疫毒性的影响。选择暴露浓度以便使用基于质量和基于颗粒表面积的暴露指标进行数据评估。选择的nano-C60暴露水平为0.5和2毫克/立方米(0.033和0.112百万分率),而micro-C60暴露水平为2、15和30毫克/立方米(0.011、0.084和0.167百万分率)。对先天免疫、细胞介导免疫或体液免疫功能均无全身影响。肺部炎症反应(组织细胞浸润、巨噬细胞色素沉着、慢性炎症)呈浓度依赖性,与支气管肺泡灌洗(BAL)液中单核细胞趋化蛋白(MCP)-1(大鼠)和巨噬细胞炎症蛋白(MIP)-1α(小鼠)的增加相对应。肺部超载可能是导致在2毫克/立方米的nano-C60暴露和30毫克/立方米的micro-C60暴露后观察到的肺部炎症反应的原因。在所有暴露于C60的大鼠中,无论暴露水平如何,从BAL中回收的细胞的表型也发生了变化。总体而言,在基于质量的暴露比较中,观察到nano-C60比micro-C60对肺部的影响更严重。然而,对于基于表面积的暴露,观察到micro-C60比nano-C60对肺部的影响更严重,这突出了在评估纳米颗粒和微米颗粒之间的毒性时剂量测定的重要性。