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未修饰纳米SiO_2和表面修饰型纳米SiO_2对大鼠肺泡巨噬细胞的毒性研究 被引量:5

Study on cytotoxicity of nanosized silica and surface modified nanosized silica in rat alveolar macrophages
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摘要 目的:比较未修饰纳米SiO2和表面修饰型纳米SiO2对大鼠肺泡巨噬细胞的毒性。方法:通过支气管肺泡灌洗分离雄性SD大鼠肺泡巨噬细胞。未修饰纳米SiO2(M-5型)及两种表面修饰型纳米SiO2(TS-610型,TS-720型)剂量分别为0,8,40,100,200μg/cm2,用MTT实验测定对细胞活性的影响,LDH实验测定对细胞膜的损伤,TBA法测定脂质过氧化作用的程度。结果:M-5型纳米SiO2在剂量大于100μg/cm2时,各指标与对照组相比有统计学意义(P<0.05),而两种表面修饰型纳米SiO2与对照组相比均无统计学意义。结论:未修饰纳米SiO2对大鼠肺泡巨噬细胞的毒性较强,颗粒表面被修饰后其毒性明显降低,表明颗粒表面反应性在毒性机制中发挥重要作用。 Objective: To compare the cytotoxicity of nanosized silica and surface modified nanosized silica in rat alveolar macrophages. Methods: Male SD rat alveolar macrophages isolated by bronchoalveolar lavage were exposed to nanosized silica (M-5) and surface modified nanosized silica (TS-610, TS-720) at doses of 0, 8, 40, 100, 200 μg/cm2. The cell activity was tested by MTr assay, injury to membrane by LDH assay and lipid peroxidation by TBA method. Results: For the three indices M-5 nanosized silica had significant difference from control when doses were higher than 100 μg/cm2 ( P 〈 0.05 ), whereas surface modified nanosized silica had no significant difference from control at all doses. Condusion: M-5 nanosized silica was more toxic to alveolar macrophages. The apparent decrease of cytotoxicity after surface modification indicated the important role of surface reactivity in the cytotoxicity of nanosized silica.
出处 《江苏大学学报(医学版)》 CAS 2007年第1期53-56,共4页 Journal of Jiangsu University:Medicine Edition
关键词 纳米SIO 表面修饰 大鼠 肺泡巨噬细胞 毒性 nanosized silica surface modification rat alveolar macrophage toxicity
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  • 1Colvin VL. The potential environmental impact of engineered nanomaterials [ J ]. Nat Bioteehnol, 2003, 21(10): 1166-1170.
  • 2Whitesides GM. The fight size in nanobiotechnology[ J].Nat Biotechnol, 2003, 21(10) : 1161 -1165.
  • 3Roco MC. Environmentally responsible development of nanotechnology [ J ]. Environ Sci Technol, 2005, 39(5): 106A - 112A.
  • 4Renwick LC, Brown D, Clouter A, et al. Increased inflammation and altered macrophage chemotactic responses caused by two uhrafine particle types [ J ]. Occup Environ Med, 2004, 61(5): 442-447.
  • 5Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays[J]. J Immunol Methods, 1983, 65(1 -2): 55- 63.
  • 6Renwick LC, Donaldson K, Clouter A. Impairment of alveolar macrophage phagoeytosis by ultrafine particles[J]. Toxicol Appl Pharmacol, 2001, 172(2): 119 -127.
  • 7Schins RP,Duffin R, Hohr D, et al. Surface modification of quartz inhibits toxicity, particle uptake, and oxidative DNA damage in human lung epithelial cells[J].Chem Res Toxieol, 2002, 15(9) : 1166 -1173.
  • 8Knaapen AM,Albrecht C, Becker A, et al. DNA damage in lung epithelial cells isolated from rats exposed to quartz : role of surface reactivity and neutrophilic inflammation[J]. Carcinogenesis, 2002, 23 ( 7 ) : 1111 -1120.

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