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基于脂质体的纳米基因载体的研究进展 被引量:18

Research Progress of Nano-Gene Carriers Based on Liposomes
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摘要 基因治疗是指将外源基因导入目标细胞,用以修正因基因缺陷和异常导致的疾病,达到治疗疾病的目的。外源基因在细胞中高效、持续地表达是基因治疗成功的关键,这与载体的选择息息相关。随着科技的发展,脂质体纳米复合物作为基因载体受到人们广泛关注,其具有功能多样、易于修饰、生物相容性好、转染效率高等优点。本文介绍了脂质体的结构特点,并对磁性纳米、金纳米、量子点、壳聚糖、上转换纳米与脂质体的复合物作为基因载体进行综述和展望。 Gene therapy is a method for curing diseases caused by genetic defects and anomalies through introducing normal foreign genes into targeted cells. Efficient and sustained expression of foreign genes in cells is the decisive factor in gene therapy,which is significantly relied on the vectors used in the treatment. With the development of science and technology,the research of liposome/nanocomposites as gene carriers has widely attracted people' s attention, due to the following advantages: versatile functions, easy surface modification,good biocompatibility,high transfection efficiency. Herein,the structure of liposome bilayer was introduced and the complexes of magnetic nanoparticles, gold nanoparticles, quantum dots, chitosan,upconversion nanoparticles with liposomes as gene carriers have been reviewed and prospected.
作者 韩旭 丁冠宇 董青 李云辉 杨秀云 李丹 杜衍 汪尔康 HAN Xu;DING Guanyu;DONG Qing;YANG Xiuyun;LI Dan;DU Yan;WANG Erkang(Key Laboratory of Preparation and Applications of EnvironmentalFriendly Materials,Jilin Normal University,Changchun 130103,China;State Key Laboratory of Rare Earth Resource Utilization,Changchun Institute of Applied Chemistry,CAS,Changchun 130022,China;Department of Chemistry,University of Science and Technology of China,Hefei 230026,China;Jiangxi Jiangwu Haoyun High-tech Co.,Ltd,Nanchang 330096,China)
出处 《应用化学》 CAS CSCD 北大核心 2018年第7期735-744,共10页 Chinese Journal of Applied Chemistry
关键词 脂质体 基因载体 纳米材料 liposome gene carrier nanomaterials
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  • 1刘凯,王昆,黄复生.前列腺素E_1脂质体的制备及稳定性初步研究[J].中国药业,2005,14(2):46-48. 被引量:6
  • 2黎维勇,宋波,陈华庭.新型阿霉素热敏脂质体的研制[J].中国医院药学杂志,2005,25(5):439-441. 被引量:6
  • 3李菲,高允生.新型脂质体的研究进展[J].泰山医学院学报,2005,26(5):502-503. 被引量:4
  • 4王海刚,翟光喜,吕青志,凌沛学.壳聚糖包覆葛根素脂质体的制备及理化性质考察[J].中药材,2007,30(1):89-92. 被引量:10
  • 5COUVREUR P, PATI E, MALVY C, et al. PH-sensitive lioposomes: all intelligent system for delivery of antisense oligonuvleotides [J]. J Li Pesome Res,1997 ,7(1) :1.
  • 6DUZGUNES N, PRETZER E, SIMOES S, et al. Liposome mediated delivery of antiviral agents to human immunodeficiency virus infected ceils [J] .J Mol Membr Biol,1999,16( 1 ) :111.
  • 7BETAGERL G V, JENKINS S A,PARSONS D L. In liposome drug delivery systems [ M J// Betageri G V, eds. Targeting of pH- sensitive lioposomes. Pennysy Ivania(USA) :Technomic. 1993:103 .
  • 8TENU J P, SEKKAI D, YAPO A, et al. Phosphatidy-linositolman- noside-based liposomes induce no synthase in primed mouse peritoneal macrophages [ J ] . J Biochem Biophys Res Commun, 1995,208( 1 ) :295.
  • 9KAKINUMA K, TANAKA R, TAKAHASHI H, et al. Drug delivery to the brain using themosensive liposome and local hyperthemia [ J] . Int J Hyperthemia, 1996, 12(1): 157-165.
  • 10OKU K, NARUSC R, DOI K, et al. Potential usage of thermo sensitive liposomes for macromolecule delivery [ J]. Biochim Biop Hys Acts, 1994(19) :389 -393.

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