Key issues in non-viral gene delivery (Reprinted from Advanced Drug Delivery Reviews, vol 34, pg 3-19, 1998)

被引:285
作者
Pouton, CW [1 ]
Seymour, LW
机构
[1] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[2] Univ Birmingham, CRC, Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
关键词
gene therapy; DNA delivery; virus-like particles; DNA condensation; biopharmaceutics;
D O I
10.1016/S0169-409X(00)00133-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The future of non-viral gene therapy depends on a detailed understanding of the barriers to delivery of polynucleotides. These include physicomechanical barriers, which Limit the design of delivery devices, physicochemical barriers that influence self-assembly of colloidal particulate formulations, and biological barriers that compromise delivery of the DNA to its target site. It is important that realistic delivery strategies are adopted for early clinical trials in non-viral gene therapy. In the longer term, it should be possible to improve the efficiency of gene delivery by learning from the attributes which viruses have evolved; attributes that enable translocation of viral components across biological membranes. Assembly of stable, organized virus-like particles will require a higher level of control than current practice. Here, we summarize present knowledge of the biodistribution and cellular interactions of gene delivery systems and consider how improvements in gene delivery will be accomplished in the future. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:187 / 203
页数:17
相关论文
共 124 条
[121]   ADENOVIRUS-MEDIATED GENE-TRANSFER TRANSIENTLY CORRECTS THE CHLORIDE TRANSPORT DEFECT IN NASAL EPITHELIA OF PATIENTS WITH CYSTIC-FIBROSIS [J].
ZABNER, J ;
COUTURE, LA ;
GREGORY, RJ ;
GRAHAM, SM ;
SMITH, AE ;
WELSH, MJ .
CELL, 1993, 75 (02) :207-216
[122]   CELLULAR AND MOLECULAR BARRIERS TO GENE-TRANSFER BY A CATIONIC LIPID [J].
ZABNER, J ;
FASBENDER, AJ ;
MONINGER, T ;
POELLINGER, KA ;
WELSH, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (32) :18997-19007
[123]   Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis [J].
Zabner, J ;
Ramsey, BW ;
Meeker, DP ;
Aitken, ML ;
Balfour, RP ;
Gibson, RL ;
Launspach, J ;
Moscicki, RA ;
Richards, SM ;
Standaert, TA ;
WilliamsWarren, J ;
Wadsworth, SC ;
Smith, AE ;
Welsh, MJ .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (06) :1504-1511
[124]   Expression of naked plasmid DNA injected into the afferent and efferent vessels of rodent and dog livers [J].
Zhang, GF ;
Vargo, D ;
Budker, V ;
Armstrong, N ;
Knechtle, S ;
Wolff, JA .
HUMAN GENE THERAPY, 1997, 8 (15) :1763-1772