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PEG-PE载药胶束的体内分布与毒性研究

Study of the biodistribution and toxicity of doxorubicin encapsulated in PEG-PE micelles in mice

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【作者】 魏秀莉汪贻广曾文峰张硕于丽娟秦蕾张春玲梁伟

【Author】 WEI Xiu-li,WANG Yi-guang,ZENG Wen-feng,ZHANG Shuo,YU Li-juan,QIN Lei,ZHANG Chun-ling,LIANG Wei(Institute of Biophysics,Chinese Academy of Sciences,Beijing 100101,China)

【机构】 中国科学院生物物理研究所

【摘要】 目的:研究PEG-PE载药胶束静脉给药后在动物体内的分布与毒性。方法:采用一步自组装法制备载阿霉素的单一PEG-PE胶束或加入卵磷脂(HSPC)的混合胶束(M-Doxs);用BALB/c小鼠考察PEG-PE载药胶束的体内分布以及对动物生化指标及脏器的影响。结果:制备了3种不同粒径的载药胶束:M1-Dox[PEG-PE/HSPC=1∶0,(14.5±1.2)nm]、M2-Dox[PEG-PE/HSPC=1∶0.5,(22.4±0.9)nm]与M3-Dox[PEG-PE/HSPC=1∶1,(34.2±1.3)nm]。加入HSPC后胶束的形貌由球形逐渐变为棒状结构。M-Doxs在肝、肺、肾及肿瘤中的分布呈粒径依赖性。在22.5 mg.kg-1剂量下,M1-Dox与M3-Dox组的动物生存期明显延长。M-Doxs可显著降低对动物的全身毒性。结论:粒子的大小与形貌可改变M-Doxs在体内的分布,减轻药物的全身毒性。通过对纳米载药系统的物理化学性质进行修饰,可改变其在体内的行为。

【Abstract】 Objective:To investigate the biodistribution and acute toxicity of doxorubicin loaded in PEG-PE based micelles(M-Doxs)for mice through the tail vein injection.Methods: Doxorubicin was loaded in the simple or mixed micelles made from polyethylene glycol-phosphatidylethanolamine alone(PEG-PE)or combined with hydrogenated phosphatidylcholine(HSPC)by a self-assembly procedure.Different doses of free doxorubicin(F-Dox)and equivalent doses of M-Doxs were intravenously in mice to compare their biodistribution and acute toxicities.Results: The increased molar ratios of HSPC in the PEG-PE based micelles increase the particle size(one dimension elongation)and change their shapes from the spherical to the worm like-rod.The mean sizes of M1-Dox(PEG-PE/HSPC=1∶0),M2-Dox(PEG-PE/HSPC=1∶0.5)and M3-Dox(PEG-PE/HSPC=1∶1)are(14.5±1.2)nm,(22.4±0.9)nm,and(34.2±1.3)nm,respectively.Biodistribution of M-Doxs showed a significantly size and shape-depended accumulation in liver,lung,kidney and tumor.M1-Dox and M2-Dox exhibited higher drug concentration in serum and lymph node,while M1-Dox showed the lowest drug concentration in heart.Compared with F-Dox,M-Doxs had shown the low systemic toxicity.The survival time of mice in the groups of M1-Dox and M3-Dox was markedly prolongation compared with F-Dox at the dose of 22.5 mg·kg-1.Conclusion: The size and shape of doxorubicin loaded-micelles significantly influenced the behaviors,toxicity of doxorubicin in vivo.It is to be come true that controlling drug behavior in vivo by modifying the physicochemical properties of nano-carriers to implement diverse therapeutic requirements in clinic.

【基金】 国家重点基础研究计划项目(2007CB935801);国家自然科学基金资助项目(30901869)
  • 【文献出处】 东南大学学报(医学版) ,Journal of Southeast University(Medical Science Edition) , 编辑部邮箱 ,2011年01期
  • 【分类号】R94
  • 【被引频次】2
  • 【下载频次】593
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