中国科学技术大学学报 ›› 2015, Vol. 45 ›› Issue (5): 366-372.DOI: 10.3969/j.issn.0253-2778.2015.05.004

• 原创论文 • 上一篇    下一篇

Zn0.4Fe2.6O4纳米颗粒对小鼠肺毒性效应

祝闪闪   

  1. 中国科学技术大学化学系,安徽合肥 230026
  • 收稿日期:2015-03-25 修回日期:2015-05-01 出版日期:2015-05-31 发布日期:2015-05-31
  • 作者简介:ZHU Shanshan, female, born in 1989, master. Research field: toxicity of nanomaterials. E-mail: ssz2008@mail.ustc.edu.cn

Evaluation of pulmonary toxicity of zinc-doped magnetite nanoparticle in mice after intragastric administration

ZHU Shanshan   

  1. Department of Chemistry, University of Science and Technology of China, Hefei 230026, China
  • Received:2015-03-25 Revised:2015-05-01 Online:2015-05-31 Published:2015-05-31
  • Contact: XU Xiaolong

摘要: 锌掺杂的磁性纳米颗粒(ZnaFebO4 NPs)比常规的磁性纳米颗粒(Fe3O4 NPs)具有更高的磁化率.合成了二巯基丁二酸(DMSA)包裹的Zn0.4Fe2.6O4 纳米颗粒(NPs),并研究了Zn0.4Fe2.6O4 NPs灌胃给药对小鼠肺的毒性效应.在整个灌胃给药一个月的实验过程中,对照组和实验组的小鼠均无异常现象发生.灌胃给药Zn0.4Fe2.6O4 NPs以后,Fe在小鼠的肺内聚积.肺内Fe的聚积导致肺的脏器系数增加.Zn0.4Fe2.6O4 NPs灌胃给药除了引起肺组织非常轻微的炎症反应以外,没有对肺产生明显的损伤.实验结果表明, DMSA包裹的Zn0.4Fe2.6O4 NPs毒性低,可以作为口服的药物载体或成像的造影剂.

关键词: 磁性纳米颗粒, Zn, 毒性, 组织切片, 灌胃

Abstract: Zn2+ doped magnetite nanoparticles (ZnaFebO4 NPs) have higher magnetic susceptibility than conventional magnetite nanoparticles (Fe3O4 NPs). Dimercaptosuccinic acid (DMSA)-coated Zn0.4Fe2.6O4 nanoparticles (Zn0.4Fe2.6O4 NPs) were synthesized. The pulmonary toxicity of DMSA-coated Zn0.4Fe2.6O4 NPs in mice was evaluated after oral administration for one month. No abnormal activities among the mice were observed in Zn0.4Fe2.6O4 NPs-treated group during the whole experiment process. The accumulation of Fe in the lungs was observed after oral administration of DMSA-coated Zn0.4Fe2.6O4 NPs in mice. The accumulation of Fe in the lungs resulted in an increase of coefficient of lung, but did not cause obvious pulmonary injury, except for a very slight inflammatory response in the tissue. The results show that low toxic DMSA-coated Zn0.4Fe2.6O4 NPs may be used as drug delivery or imaging contrast agents by oral route.

Key words: magnetite nanoparticle, Zn, toxicity, histopathology, intragastric administration