Baker Gregory L, Gupta Amit, Clark Mark L, Valenzuela Blandina R, Staska Lauren M, Harbo Sam J, Pierce Judy T, Dill Jeffery A
Battelle Toxicology Northwest, Richland, Washington 99354, USA.
Toxicol Sci. 2008 Jan;101(1):122-31. doi: 10.1093/toxsci/kfm243. Epub 2007 Sep 17.
While several recent reports have described the toxicity of water-soluble C60 fullerene nanoparticles, none have reported the toxicity resulting from the inhalation exposures to C60 fullerene nanoparticles or microparticles. To address this knowledge gap, we exposed male rats to C60 fullerene nanoparticles (2.22 mg/m3, 55 nm diameter) and microparticles (2.35 mg/m3, 0.93 microm diameter) for 3 h a day, for 10 consecutive days using a nose-only exposure system. Nanoparticles were created utilizing an aerosol vaporization and condensation process. Nanoparticles and microparticles were subjected to high-pressure liquid chromatography (HPLC), XRD, and scanning laser Raman spectroscopy, which cumulatively indicated no chemical modification of the C60 fullerenes occurred during the aerosol generation. At necropsy, no gross or microscopic lesions were observed in either group of C60 fullerene exposures rats. Hematology and serum chemistry results found statistically significant differences, although small in magnitude, in both exposure groups. Comparisons of bronchoalveolar (BAL) lavage fluid parameters identified a significant increase in protein concentration in rats exposed to C60 fullerene nanoparticles. BAL fluid macrophages from both exposure groups contained brown pigments, consistent with C60 fullerenes. C60 lung particle burdens were greater in nanoparticle-exposed rats than in microparticle-exposed rats. The calculated lung deposition rate and deposition fraction were 41 and 50% greater, respectively, in C60 fullerene nanoparticle-exposed group than the C60 fullerene microparticle-exposed group. Lung half-lives for C60 fullerene nanoparticles and microparticles were 26 and 29 days, respectively. In summary, this first in vivo assessment of the toxicity resulting from inhalation exposures to C60 fullerene nanoparticles and microparticles found minimal changes in the toxicological endpoints examined. Additional toxicological assessments involving longer duration inhalation exposures are needed to develop a better and more conclusive understanding of the potential toxicity of inhaled C60 fullerenes whether in nanoparticle or microparticle form.
虽然最近有几份报告描述了水溶性C60富勒烯纳米颗粒的毒性,但尚无报告提及吸入C60富勒烯纳米颗粒或微粒所导致的毒性。为填补这一知识空白,我们使用仅经鼻暴露系统,让雄性大鼠每天暴露于C60富勒烯纳米颗粒(2.22毫克/立方米,直径55纳米)和微粒(2.35毫克/立方米,直径0.93微米)中,持续10天,每天暴露3小时。纳米颗粒通过气溶胶蒸发和冷凝过程制备。纳米颗粒和微粒经过高压液相色谱(HPLC)、XRD和扫描激光拉曼光谱分析,结果累计表明在气溶胶生成过程中C60富勒烯未发生化学改性。尸检时,两组C60富勒烯暴露大鼠均未观察到大体或微观病变。血液学和血清化学结果显示,两个暴露组均存在统计学上显著的差异,尽管差异幅度较小。支气管肺泡(BAL)灌洗液参数比较发现,暴露于C60富勒烯纳米颗粒的大鼠蛋白质浓度显著增加。两个暴露组的BAL液巨噬细胞均含有棕色色素,与C60富勒烯一致。纳米颗粒暴露组大鼠的C60肺颗粒负荷高于微粒暴露组大鼠。计算得出,C60富勒烯纳米颗粒暴露组的肺沉积率和沉积分数分别比C60富勒烯微粒暴露组高41%和50%。C60富勒烯纳米颗粒和微粒的肺半衰期分别为26天和29天。总之,这项对吸入C60富勒烯纳米颗粒和微粒所导致毒性的首次体内评估发现,所检查的毒理学终点变化极小。需要进行涉及更长时间吸入暴露的额外毒理学评估,以更好、更确凿地了解吸入的C60富勒烯无论是纳米颗粒形式还是微粒形式的潜在毒性。