Molecular design of functional polymers for gene therapy

被引:222
作者
Jeong, Ji Hoon
Kim, Sung Wan
Park, Tae Gwan [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[2] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
[3] Hanyang Univ, Dept Bioengn, Seoul 133971, South Korea
基金
美国国家卫生研究院;
关键词
gene delivery; cationic polymers; nonviral carriers; polylexes; POLYION COMPLEX MICELLES; WATER-SOLUBLE LIPOPOLYMER; INDUCED PHASE-SEPARATION; POLY(2-(DIMETHYLAMINO)ETHYL METHACRYLATE)-BASED POLYPLEXES; OLIGONUCLEOTIDE-POLYETHYLENIMINE COMPLEXES; DNA/TRANSFERRIN-PEI COMPLEXES; FOLATE-GRAFT-POLYETHYLENIMINE; TISSUE ENGINEERING SCAFFOLDS; CHITOSAN-DNA NANOPARTICLES; MURINE CARDIAC TRANSPLANTS;
D O I
10.1016/j.progpolymsci.2007.05.019
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In the post genomic era, massive genetic information of the human being accelerates the identification of target genes for treating various diseases. A wide range of nucleic acid therapeutics have recently emerged as powerful new drug entities for treatment of gene-related diseases and for lead validation in the drug discovery process. The absence of an efficient delivery system for genetic drugs has been identified as a major hurdle for clinical applications. Various bio-mimicking polymers have been considered as potential nonviral carriers for gene therapy due to their safety in clinical use, despite their lower gene-transduction capacity compared to virus-based gene carriers that hold risk of potential immunogenicity and endogenous virus recombination. Improving specificity toward target cells and intracellular gene-transferring efficiency will be a prerequisite for successful clinical application of polymeric gene carriers. Multifunctional polymeric gene delivery carriers should be rationally designed at the molecular level for effective human gene therapy. (C) 2007 Published by Elsevier Ltd.
引用
收藏
页码:1239 / 1274
页数:36
相关论文
共 286 条
[1]   A powerful nonviral vector for in vivo gene transfer into the adult mammalian brain: Polyethylenimine [J].
Abdallah, B ;
Hassan, A ;
Benoist, C ;
Goula, D ;
Behr, JP ;
Demeneix, BA .
HUMAN GENE THERAPY, 1996, 7 (16) :1947-1954
[2]   Augmentation of myocardial transfection using TerplexDNA: a novel gene delivery system [J].
Affleck, DG ;
Yu, L ;
Bull, DA ;
Bailey, SH ;
Kim, SW .
GENE THERAPY, 2001, 8 (05) :349-353
[3]   Synthesis of biodegradable multi-block copolymers of poly(L-lysine) and poly(ethylene glycol) as a non-viral gene carrier [J].
Ahn, CH ;
Chae, SY ;
Bae, YH ;
Kim, SW .
JOURNAL OF CONTROLLED RELEASE, 2004, 97 (03) :567-574
[4]   Parallel synthesis and biophysical characterization of a degradable polymer library for gene delivery [J].
Akinc, A ;
Lynn, DM ;
Anderson, DG ;
Langer, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (18) :5316-5323
[5]  
Akinc A, 2002, BIOTECHNOL BIOENG, V78, P503, DOI 10.1002/bit.20215
[6]   A polymer library approach to suicide gene therapy for cancer [J].
Anderson, DG ;
Peng, WD ;
Akinc, A ;
Hossain, N ;
Kohn, A ;
Padera, R ;
Langer, R ;
Sawicki, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (45) :16028-16033
[7]   Semi-automated synthesis and screening of a large library of degradable cationic polymers for gene delivery [J].
Anderson, DG ;
Lynn, DM ;
Langer, R .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (27) :3153-3158
[8]   BIODEGRADABLE MICROSPHERES .5. STIMULATION OF MACROPHAGES WITH MICROPARTICLES MADE OF VARIOUS POLYSACCHARIDES [J].
ARTURSSON, P ;
ARRO, E ;
EDMAN, P ;
ERICSSON, JLE ;
SJOHOLM, I .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1987, 76 (02) :127-133
[9]   Enhancement of the polycation-mediated DNA uptake and cell transfection with pluronic P85 block copolymer [J].
Astafieva, I ;
Maksimova, I ;
Lukanidin, E ;
Alakhov, V ;
Kabanov, A .
FEBS LETTERS, 1996, 389 (03) :278-280
[10]  
Bastos R, 1995, INT REV CYTOL, V162B, P257