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脂质体作为钆中子俘获治疗肿瘤药物载体的跨膜动力学及机理研究

Kinetics and Mechanism Study of Across-Membrane Transport of Liposome as a Carrier for Gadolinium Neutron Capture Therapy

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【作者】 邹娟任春李铁军陈丽蓉王祥云刘元方

【Author】 ZOU Juan\ REN Chun\ LI Tiejun\ CHEN Lirong\ WANG Xiangyun\ LIU Yuanfang (Division of applied Chemistry,Department of Technical Physics,Peking University,Beijing,100871)

【机构】 北京大学技术物理系应用化学专业!北京1008711008

【摘要】 制备和表征了包埋Gd EDTA的脂质体 ,测定了 pH ,离子强度 ,缓冲液组成及温度对Gd EDTA脂质体的影响 ,比较了Gd EDTA脂质体和Gd EDTA被肿瘤细胞摄入的动力学曲线。结果表明 ,Gd EDTA脂质体在 37℃和生理条件下最稳定 ,肿瘤细胞摄入Gd EDTA脂质体速率是Gd EDTA的 8倍 ,而释放Gd的速率 ,Gd EDTA脂质体远远低于Gd EDTA ,这些结果提供了脂质体包埋Gd EDTA作为钆中子俘获治疗药物的可能性。

【Abstract】 Liposome is an effective nuclide delivery agent for neutron capture therapy.In this paper liposomes containing encapsulated gadolinium complex (LGd) were prepared and characterized.The influence of formulation factors such as pH,ionic strength,buffer,and storage time upon the stability of liposomes was investigated.The uptake rate constant and its concentration dependence of LGd in tumor cells were compared in vitro with that of Gd complex itself.The results indicate that the uptake rate of LGd in tumor cells increases to eight times as much as that of Gd\|EDTA,but the release rate of Gd from tumor cells containing LGd is remarkably lower than that from the tumor cells containing Gd\|EDTA.The results reveal that LGd would be a potential drug for neutron capture therapy of cancer.

【基金】 国家科委“九·五”攀登B资助项目
  • 【文献出处】 北京大学学报(自然科学版) ,ACTA SCICENTIARUM NATURALUM UNIVERSITIS PEKINESIS , 编辑部邮箱 ,2000年06期
  • 【分类号】R73-3
  • 【被引频次】1
  • 【下载频次】135
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