Engineered Nanoscaled Polyplex Gene Delivery Systems

被引:49
作者
Fernandez, Christian A. [1 ]
Rice, Kevin G. [1 ]
机构
[1] Univ Iowa, Coll Pharm, Div Pharmaceut, Iowa City, IA 52242 USA
关键词
Oligonucleotide delivery; polyplex; lipoplex; nanoparticles; delivery barriers; ENHANCE TRANSFECTION EFFICIENCY; LOCALIZATION SIGNAL PEPTIDE; IN-VIVO; PLASMID DNA; MOLECULAR-WEIGHT; INTRACELLULAR DELIVERY; LONG-TERM; NAKED DNA; HYDRODYNAMIC INJECTION; NANOMETRIC PARTICLES;
D O I
10.1021/mp900033j
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Improving the transfection efficiencies of nonviral gene delivery requires properly engineered nanoscaled delivery carriers that can overcome the multiple barriers associated with the delivery of oligonucleotides from the site of administration to the nucleus or cytoplasm of the target cell. This article reviews the current advantages and limitation of polyplex nonviral delivery systems, including the apparent barriers that limit gene expression efficiency compared to physical methods such as hydrodynamic dosing and electroporation. An emphasis is placed on engineered nanoscaled polyplexes (NSPs) of modular design that both self-assemble and systematically disassemble at the desired stage of delivery. It is suggested that NSPs of increasingly sophisticated designs are necessary to improve the efficiency of the rate limiting steps in gene delivery.
引用
收藏
页码:1277 / 1289
页数:13
相关论文
共 136 条
[21]   Cell-penetrating peptides: tools for intracellular delivery of therapeutics [J].
Deshayes, S ;
Morris, MC ;
Divita, G ;
Heitz, F .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (16) :1839-1849
[22]   Dendrimers in gene delivery [J].
Dufès, C ;
Uchegbu, IF ;
Schätzlein, AG .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (15) :2177-2202
[23]  
DVORAK HF, 1988, AM J PATHOL, V133, P95
[24]   The silent treatment: siRNAs as small molecule drugs [J].
Dykxhoorn, DM ;
Palliser, D ;
Lieberman, J .
GENE THERAPY, 2006, 13 (06) :541-552
[25]  
Erbacher P, 1999, J GENE MED, V1, P210
[26]   Efficient Non-Viral Ocular Gene Transfer with Compacted DNA Nanoparticles [J].
Farjo, Rafal ;
Skaggs, Jeff ;
Quiambao, Alexander B. ;
Cooper, Mark J. ;
Naash, Muna I. .
PLOS ONE, 2006, 1 (01)
[27]   Improved cationic lipid formulations for in vivo gene therapy [J].
Felgner, PL ;
Tsai, YJ ;
Sukhu, L ;
Wheeler, CJ ;
Manthorpe, M ;
Marshall, J ;
Cheng, SH .
DNA VACCINES: A NEW ERA IN VACCINOLOGY, 1995, 772 :126-139
[28]   GENE THERAPEUTICS [J].
FELGNER, PL ;
RHODES, G .
NATURE, 1991, 349 (6307) :351-352
[29]   Towards safe, non-viral therapeutic gene expression in humans [J].
Glover, DJ ;
Lipps, HJ ;
Jans, DA .
NATURE REVIEWS GENETICS, 2005, 6 (04) :299-U29
[30]   Macropinocytosis of polyplexes and recycling of plasmid via the clathrin-dependent pathway impair the transfection efficiency of human hepatocarcinoma cells [J].
Gonçalves, C ;
Mennesson, E ;
Fuchs, R ;
Gorvel, JP ;
Midoux, P ;
Pichon, C .
MOLECULAR THERAPY, 2004, 10 (02) :373-385