Key issues in non-viral gene delivery

被引:165
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(98)00048-9
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) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:3 / 19
页数:17
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