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气管滴注纳米二氧化硅颗粒致大鼠肺炎症反应及脏器中硅浓度变化的研究 被引量:1

The Study of Pulmonary Inflammatory Reaction and Change of Si Concentration in tissues of Silica Nanoparticles in Rats after Intracheal Instillation
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摘要 目的对纳米二氧化硅颗粒导致大鼠肺脏的炎症反应进行研究。方法将128只雄性Wistar大鼠随机分为4组,分别为空白对照组(生理盐水)、0.5、1和2mg/Kg·bw剂量组,采用非暴露式气管滴注染毒一次,分别于染毒后的1d、7d、14d以及28d后处死大鼠,每实验组各处死8只动物,分别检测分析脏器中的硅浓度的变化;检测肺泡灌洗液中白细胞总数、蛋白含量、乳酸脱氢酶。结果纳米二氧化硅颗粒主要分布在肝脏和肾脏;可引起大鼠肺部明显的炎症反应;可引起肺泡灌洗液中的白细胞总数、蛋白含量、乳酸脱氢酶升高。结论纳米二氧化硅颗粒可引起肺组织损伤,对大鼠具有一定的肺毒性作用。 Objective To study the pulmonary inflammatory reaction of silica nanoparticles in rat after intracheal In- stillation. Methods 128 Wistar rats divided into 4 groups at random and exposed to blank control and different doses of exposed groups (0.5,1.0, and 2.0 mg/Kg ·bw) by intra-tracheal instillation only once. And rats were neerospied at 1 day, 7 day, 14 day, and 28 day after exposure. Si concentration of tissues for rats was detected. The bronchoalveolar lav- age fluid (BALF) was collected and analyzed; Total white cell count, total protein (TP), and lactic dehydrogenase (LDH) in lung BALF were measured. Results Silica nanoparticles are mainly distributed in the liver and kidneys; can induce significant lung inflammation,and cause total white cell count,TP, and LDH in BALF increased. Conclusion Silica nanoparticles can cause lung tissue damage in rats with a certain lung toxicity.
出处 《中国实验诊断学》 2013年第10期1779-1782,共4页 Chinese Journal of Laboratory Diagnosis
关键词 纳米二氧化硅颗粒 肺泡灌洗液 炎症指标 乳酸脱氢酶 Silica nanoparticle Bronchoalveolar lavage fluid Inflammation markers Lactic dehydrogenase
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参考文献16

  • 1张婷,唐萌.纳米颗粒吸入毒性研究进展[J].卫生研究,2008,37(5):633-636. 被引量:6
  • 2Oberdorster G, Fefin J, Lehnert BE. Correlation between particle size,in vivo particle persistence, and lung injury [J]. Environ Health Perspect, 1994,102 (Suppl 5) : 173.
  • 3Burns AA, Vier J, OW H, et al. Fluoreseeni Silica Nanoparticles with Emcient Urinary Excretion for Nanomedieine [J]. Nano Lett,2009,9(1) :442.
  • 4Sayescm,Warheitdb. Charaeterization of nanomaterials for toxie ity assessment [J]. Nanomed Nano bioteehnol, 2009,1 (6) : 660.
  • 5Murdock RC,Braydich stoll EL, Scharand AM,et al. Character- ization of nanomateriald is persioninsolution priortoin vitro expo sure using dynamic light scattering technique [J]. Toxicol Sci, 2008. 101(2) :239.
  • 6Li Y,Sun L, Sun ZW, et al. Size-dependent cytotoxicity of amor- phous silica nanoparticles in human hepatomaHepG2 cells [J]. Toxicology in Vitro,2011,25(7) : 1343.
  • 7Oberdorster G, Oberdorster E, Oberdorster J, et al. Nanotoxicolo- gy:An emergingdiscipline evolving from studies of ultrafine parti- cles[J]. Environ Health Perspect, 2005,113 (7) : 823.
  • 8Goman J. Taming high- teeh particles [J]. Science News, 2002, 161(13) ;200.
  • 9Shvedova AA,Kisin ER,Mercer R,et al. Unusnal inflammatory and fi- brogenie pulmonary responses to single-walled carbon nanotubes in mice [J]. Physieo 1Lung Cell Mol Pgysiol,2005,289(5) :698.
  • 10Hnizdo E,Vallyathan V. Chronic obstructive pulmonary disease due to occupational exposure to silica dust : a review of epidemio logical and pathological evidence [J]. VMJ, 2003,60 (4) : 237.

二级参考文献30

  • 1郭小天,孟洁,孔桦,宋礼,王超英,何朝晖,杨子彬,许海燕.碳纳米管表面的蛋白质吸附及PEG修饰研究[J].透析与人工器官,2005,16(3):5-8. 被引量:6
  • 2李俊纲,李晴暖,李文新.粒径小于3纳米的TiO2对小鼠的肺部损伤[J].纳米科技,2006,3(6):17-21. 被引量:8
  • 3PROFFITT F. Nanotechnology: yellow light for nanotech [ J]. Science, 2004,305 ( 5685 ) : 762.
  • 4OBERDORSTER G, FERIN J, LEHNERT B E. Correlation between particle size, in vivo particle persistence and lung injury [J]. Environ Health Perspect, 1994,102:173-179.
  • 5BERMUDEZ E, MANGUM J B, WONG B A, et al. Pulmonary Respones of mice, rats and hamsters to subchronic inhalation of ultrafine titanium dioxide particles [ J ]. Toxicol Sci, 2004,77 : 347-357.
  • 6BORM P J, KREYLING W. Toxicological hazards of inhaled nanoparticles-potential implications for drug delivery [J]. Nanosci Nanotechnol, 2004,4(5) :521-531
  • 7CHEN Huiwen, SU Shengfang, CHEN Changting, et al. Titanium. dioxide nanoparticles induce emphysema-like lung injury in mice [ J ]. FASEB, 2006,20 (13), 2393-2395.
  • 8LAM C W, JAMES J T, MCCLUSKEY R, et al. Pulmonary toxicity of single-wall carbon nanotubes in mice 7 and 90 days after intratracheal instillation[J]. Toxicol Sci ,2004,77 : 126-134.
  • 9WARHEIT D B, LAURENCE B R, REED K L, et al. Comparative pulmonary toxicity assessment of single-wall carbon nanotubes in rats [J]. Toxicol Sci, 2004,77 : 117-125.
  • 10SHVEDOVA A A, KISIN E R, MURRAY R, et al. Unusual inflammatory and fibrogenic pulmonary responses to single-walled carbon nanotubes in mice [J]. Am J Physiol Lung Cell Mol Physiol, 2005,289 (9) :698-170.

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