Fusogenic liposome delivers encapsulated nanoparticles for cytosolic controlled gene release

被引:67
|
作者
Kunisawa, J
Masuda, T
Katayama, K
Yoshikawa, T
Tsutsumi, Y
Akashi, M
Mayumi, T
Nakagawa, S
机构
[1] Osaka Univ, Dept Biopharmaceut, Grad Sch Pharmaceut Sci, Suita, Osaka 5650871, Japan
[2] Kagoshima Univ, Grad Sch Sci & Engn, Dept Nanostructured & Adv Mat, Kagoshima 890, Japan
关键词
fusogenic liposome; nanoparticle; nanotechnology; drug delivery; antisense oligonucleotide DNA;
D O I
10.1016/j.jconrel.2005.03.020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Therapeutic agents based on DNA or RNA oligonucleotides (e.g., antisense DNA oligonucleotide, small interfering RNA) require a regulation of their kinetics in cytoplasm to maintain an optimal concentration during the treatment period. In this respect, delivery of functional nanoparticles containing these drugs into cytoplasm has been thought to have a potential for the cytosolic controlled gene release. In this study, we establish a protocol for the encapsulation of nanoparticles into liposome, which is further fused with ultra violet-inactivated Sendai virus to compose fusogenic liposomes. When nanoparticles were encapsulated in conventional liposomes, endocytosis-mediated uptake of nanoparticles was observed. In contrast, numerous amounts of nanoparticles were delivered into the cytoplasm without any cytotoxicity when the particles were encapsulated in fusogenic liposomes. Additionally, fusogenic liposome showed a high ability to deliver nanoparticles containing DNA oligonucleotides into cytoplasm. These results indicate that this combinatorial nanotechnology using fusogenic liposome and nanoparticle is a valuable system for regulating the intracellular pharmacokinetics of gene-based drugs. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:344 / 353
页数:10
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