刘艳, 于杨, 陈杰, 岳美, 马荣爽, 赵淑华. 纳米氧化石墨烯对小鼠体内外急性毒性作用[J]. 环境卫生学杂志, 2017, 7(3): 233-238. DOI: 10.13421/j.cnki.hjwsxzz.2017.03.011
    引用本文: 刘艳, 于杨, 陈杰, 岳美, 马荣爽, 赵淑华. 纳米氧化石墨烯对小鼠体内外急性毒性作用[J]. 环境卫生学杂志, 2017, 7(3): 233-238. DOI: 10.13421/j.cnki.hjwsxzz.2017.03.011
    LIU Yan, YU Yang, CHEN Jie, YUE Mei, MA Rongshuang, ZHAO Shuhua. Acute Toxicity of Nano Graphene Oxide on Mice in Vitro and in Vivo[J]. Journal of Environmental Hygiene, 2017, 7(3): 233-238. DOI: 10.13421/j.cnki.hjwsxzz.2017.03.011
    Citation: LIU Yan, YU Yang, CHEN Jie, YUE Mei, MA Rongshuang, ZHAO Shuhua. Acute Toxicity of Nano Graphene Oxide on Mice in Vitro and in Vivo[J]. Journal of Environmental Hygiene, 2017, 7(3): 233-238. DOI: 10.13421/j.cnki.hjwsxzz.2017.03.011

    纳米氧化石墨烯对小鼠体内外急性毒性作用

    Acute Toxicity of Nano Graphene Oxide on Mice in Vitro and in Vivo

    • 摘要:
      目的 通过体内和体外实验观察氧化石墨烯纳米颗粒的急性毒性作用。
      方法 选择60只健康ICR小鼠,雌雄各半,随机分成6组,每组10只,以高纯水配制纳米氧化石墨烯,分别以剂量0 mg/(kg·bw)、3.125 mg/(kg·bw)、6.25 mg/(kg·bw)、12.5 mg/(kg·bw)、25.0 mg/(kg·bw)和50.0 mg/(kg·bw)进行纳米氧化石墨烯灌胃,观察动物一般状态及死亡情况;另取60只ICR小鼠,分为6组,在无菌条件下,以高纯水配制纳米氧化石墨烯,以剂量0 mg/(kg·bw)、1.0 mg/(kg·bw)、2.0 mg/(kg·bw)、4.0 mg/(kg·bw)、8.0 mg/(kg·bw)和16.0 mg/(kg·bw)进行尾静脉注射,观察动物一般状态及死亡情况。采用MTT法,以剂量为9.875 mg/(kg·bw)、18.75 mg/(kg·bw)、37.5 mg/(kg·bw)、75 mg/(kg·bw)、150 mg/(kg·bw)、300 mg/(kg·bw)和600 mg/(kg·bw)的氧化石墨烯与A549细胞进行共培养,观察细胞的生长状况并计算细胞的LC50
      结果 纳米氧化石墨烯经口染毒途径未引起小鼠器官病理改变,无动物死亡;通过尾静脉注射对小鼠的LD50为5.657 mg/(kg·bw),肺、肝、心组织血管内可见褐色纳米颗粒,但组织未见病理学变化;对A549细胞的LC50为56.885 μg/mL。
      结论 未经修饰的纳米氧化石墨烯经尾静脉注射可导致动物死亡,并对A549细胞生长具有抑制作用。

       

      Abstract:
      Objective To observe the acute toxicity of nano grapehene oxide on mice in vitro and in vivo.
      Methods Sixty healthy ICR mice, half male and half female, were divided into six groups and treated with nano graphene oxide dissolved in ultrapure water by intragastric administration at the dosage of 0, 3.125 mg/(kg·bw), 6.25 mg/(kg·bw), 12.5 mg/(kg·bw), 25.0 mg/(kg·bw) and 50.0 mg/(kg·bw) respectively. Another 60 ICR mice were treated with nano graphene oxide dissolved in sterile pure water at the dosage of 0, 1.0 mg/(kg·bw), 2.0 mg/(kg·bw), 4.0 mg/(kg·bw), 8.0 mg/(kg·bw) and 16.0 mg/(kg·bw) respectively by intravenous injection under aseptic condition.Meanwhile, A549 cells were co-cultured with nanograpehene oxide at the concentrations of 0, 9.875 mg/(kg·bw), 18.75 mg/(kg·bw), 37.5 mg/(kg·bw), 75 mg/(kg·bw), 150 mg/(kg·bw), 300 mg/(kg·bw), and 600 mg/(kg·bw) respectively.
      Results No pathological change of main organs had been observed in mice caused by intragastric administration of nano graphene oxide, and the LD50 was 5.657 mg/(kg·bw) of nano graphene oxide for mice caused by caudal vein injection. The LC50 of nano graphene oxide for A549 cell was 56.885 μg/mL.
      Conclusion Intravenous injection of unmodified nano graphene oxide could cause mice death and the existence of nano graphene oxide in culture medium could inhibit the survival of A549 cell.

       

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