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脑胶质瘤基因治疗载体
  • ISSN号:1000-8225
  • 期刊名称:国际肿瘤学杂志
  • 时间:2011
  • 页码:592-595
  • 分类:TQ463.7[化学工程—制药化工] Q523[生物学—生物化学]
  • 作者机构:[1]Institute of Neurological Disorders, Yuquan Hospital,Tsinghua University, Beijing 100049, China, [2]Department of Biological Pharmaceuticals, Beijing University ofChinese Medicine, Beijing 100029, China, [3]Key Laboratory of Particle & Radiation Imaging, TsinghuaUniversity, Ministry of Education, Beijing 100084, China
  • 相关基金:This work was supported by the National Nat-ural Science Foundation of China (81071885). The authors wish toacknowledge the assistance of Professor Tiande Zhao for ongoing helpful discussions and advice on experiments analysis.
  • 相关项目:功能肽修饰的磁纳米粒子用于脑胶质瘤磁感应纳米基因热疗
中文摘要:

The biocompatibility and biodistribution of magnetic nanoparticles(MNPs)in vivo are essential to ensure their safely clinical application.We have studied these aspects with our 3-aminopropyltriethoxysilanecoated magnetic nanoparticles(APTS-MNPs)formulation,which can be used as magnetic induction hyperthermia media.Changes in tissue iron levels were analyzed after intraperitoneal injection of APTS-MNPs to ICR mice.Liver and kidney functions were tested.Heart,liver,spleen,lung,kidney,testis,and brain were sectioned for pathological analysis.Biodistribution of iron in various body tissues changed with time but greater fraction of the injected iron localized in the liver and spleen than in other tissues.Serum showed an increase in AST and LDH following APTS-MNPs injection.Histological analyses of selected tissues showed no obvious abnormal changes.In conclusion,APTS-MNPs did not cause continuing changes in the liver and kidney function and thus can be safely used for in vivo application.

英文摘要:

The biocompatibility and biodistribution of magnetic nanoparticles (MNPs) in vivo are essential to ensure their safely clinical application. We have studied these aspects with our 3-aminopropyltriethoxysilane-coated magnetic nanoparticles (APTS-MNPs) formulation, which can be used as magnetic induction hyperthermia media. Changes in tissue iron levels were analyzed after intraperitoneal injection of APTS-MNPs to ICR mice. Liver and kidney functions were tested. Heart, liver, spleen, lung, kidney, testis, and brain were sectioned for pathological analysis. Biodistribution of iron in various body tissues changed with time but greater fraction of the injected iron localized in the liver and spleen than in other tissues. Serum showed an increase in AST and LDH fol-lowing APTS-MNPs injection. Histological analyses of selected tissues showed no obvious abnormal changes. In conclusion, APTS-MNPs did not cause continuing changes in the liver and kidney function and thus can be safely used for in vivo application.

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