Self-assembled nanoparticles containing hydrophobically modified glycol chitosan for gene delivery

被引:150
作者
Yoo, HS [1 ]
Lee, JE [1 ]
Chung, H [1 ]
Kwon, IC [1 ]
Jeong, SY [1 ]
机构
[1] Korea Inst Sci & Technol, Ctr Biomed Res, Seoul 136791, South Korea
关键词
gene delivery; chitosan; self-assembled; in vivo transfection;
D O I
10.1016/j.jconrel.2004.11.033
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A self-assembled nanoparticle was prepared using a hydrophobically modified glycol chitosan for gene delivery. A primary amine of glycol chitosan was modified with 5 beta-cholanic acid to prepare a hydrophobically modified glycol chitosan (HGC). The modified chitosan spontaneously formed DNA nanoparticles by a hydrophobic interaction between HGC and hydrophobized DNA. As the HGC content increased, the encapsulation efficiencies of DNA increased while the size of HGC nanoparticles decreased. Upon increasing HGC contents, HGC nanoparticle became less cytotoxic. The increased HGC contents also facilitated endocytic uptakes of HGC nanoparticles by COS-1 cells, which were confirmed by a confocal microscopy. The HGC nanoparticles showed increasing in vitro transfection efficiencies in the presence serum. In vivo results also showed that the HGC nanoparticles had superior transfection efficiencies to naked DNA and a commercialized transfection agent. The HGC nanoparticles composed of hydrophobized DNA and hydrophobically modified glycol chitosan played a significant role in enhancing transfection efficiencies in vitro as well as in vivo. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:235 / 243
页数:9
相关论文
共 20 条
[1]   Uptake of oligonucleotide-loaded nanoparticles in prostatic cancer cells and their intracellular localization [J].
Berton, M ;
Benimetskaya, L ;
Allémann, E ;
Stein, CA ;
Gurny, R .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1999, 47 (02) :119-123
[2]   Highly loaded nanoparticulate carrier using an hydrophobic antisense oligonucleotide complex [J].
Berton, M ;
Allémann, E ;
Stein, CA ;
Gurny, R .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1999, 9 (02) :163-170
[3]   Chitosan-based vector/DNA complexes for gene delivery: Biophysical characteristics and transfection ability [J].
Erbacher, P ;
Zou, SM ;
Bettinger, T ;
Steffan, AM ;
Remy, JS .
PHARMACEUTICAL RESEARCH, 1998, 15 (09) :1332-1339
[4]  
Garnett MC, 1999, CRIT REV THER DRUG, V16, P147
[5]   Synthesis of triarmed poly(ethylene oxide)-deoxycholic acid conjugate and its micellar characteristics [J].
Huh, KM ;
Lee, KY ;
Kwon, IC ;
Kim, YH ;
Kim, C ;
Jeong, SY .
LANGMUIR, 2000, 16 (26) :10566-10568
[6]   Mechanism of cell transfection with plasmid/chitosan complexes [J].
Ishii, T ;
Okahata, Y ;
Sato, T .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2001, 1514 (01) :51-64
[7]   In vivo gene transfer to the mouse nasal cavity mucosa using a stable cationic lipid emulsion [J].
Kim, TW ;
Chung, H ;
Kwon, IC ;
Sung, HC ;
Jeong, SY .
MOLECULES AND CELLS, 2000, 10 (02) :142-147
[8]   Physicochemical characteristics of self-assembled nanoparticles based on glycol chitosan bearing 5β-cholanic acid [J].
Kwon, S ;
Park, JH ;
Chung, H ;
Kwon, IC ;
Jeong, SY ;
Kim, IS .
LANGMUIR, 2003, 19 (24) :10188-10193
[9]  
LANASANIFAR A, 2001, J CONTROL RELEASE, V77, P155
[10]   Preparation of chitosan self-aggregates as a gene delivery system [J].
Lee, KY ;
Kwon, IC ;
Kim, YH ;
Jo, WH ;
Jeong, SY .
JOURNAL OF CONTROLLED RELEASE, 1998, 51 (2-3) :213-220