Recent progress in polymeric gene delivery systems

被引:52
作者
Anwer, K [1 ]
Rhee, BG [1 ]
Mendiratta, SK [1 ]
机构
[1] Express Genet Inc, Huntsville, AL 35801 USA
来源
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS | 2003年 / 20卷 / 04期
关键词
gene therapy; nonviral gene delivery; functionalized polymers;
D O I
10.1615/CritRevTherDrugCarrierSyst.v20.i4.10
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Considerable progress in polymeric gene delivery systems has been made over the last several years. First generation polymers have been replaced by safer and more efficient carrier systems through molecular functionalization, improving polymer biocompatibility, biological stability, cell-specificity, and intracellular trafficking. Many new polymers have moved from in vitro characterization to preclinical validation in animal models of cancer, diabetes, and cardiovascular disorders. Although the transfection efficiency of most polymeric carriers is still significantly lower than that of viral vectors, their structural flexibility allows for continued improvement in polymer activity. Also, simple manufacturing and scale-up schemes and the low cost of manufacturing are likely to eventually compensate for the performance gap between viral and polymeric vectors and establish clinical recognition and commercialization of polymer-based gene therapy drugs.
引用
收藏
页码:249 / 293
页数:45
相关论文
共 228 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]   Stability of peptide condensed plasmid DNA formulations [J].
Adami, RC ;
Collard, WT ;
Gupta, SA ;
Kwok, KY ;
Bonadio, J ;
Rice, KG .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (06) :678-683
[3]   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
[4]   Biodegradable poly (ethylenimine) for plasmid DNA delivery [J].
Ahn, CH ;
Chae, SY ;
Bae, YH ;
Kim, SW .
JOURNAL OF CONTROLLED RELEASE, 2002, 80 (1-3) :273-282
[5]   Glucose-regulated insulin production in hepatocytes [J].
Alam, T ;
Sollinger, HW .
TRANSPLANTATION, 2002, 74 (12) :1781-1787
[6]   Expression of biologically active human insulin-like growth factor-I following intramuscular injection of a formulated plasmid in rats [J].
Alila, H ;
Coleman, M ;
Nitta, H ;
French, M ;
Anwer, K ;
Liu, QS ;
Meyer, T ;
Wang, JJ ;
Mumper, R ;
Oubari, D ;
Long, S ;
Nordstrom, J ;
Rolland, A .
HUMAN GENE THERAPY, 1997, 8 (15) :1785-1795
[7]   Systemic effect of human growth hormone after intramuscular injection of a single dose of a muscle-specific gene medicine [J].
Anwer, K ;
Shi, M ;
French, MF ;
Muller, SR ;
Chen, W ;
Liu, QS ;
Proctor, BL ;
Wang, JJ ;
Mumper, RJ ;
Singhal, A ;
Rolland, AP ;
Alila, HW .
HUMAN GENE THERAPY, 1998, 9 (05) :659-670
[8]   Polyethylenimine-mediated gene transfer into pancreatic tumor dissemination in the murine peritoneal cavity [J].
Aoki, K ;
Furuhata, S ;
Hatanaka, K ;
Maeda, M ;
Remy, JS ;
Behr, JP ;
Terada, M ;
Yoshida, T .
GENE THERAPY, 2001, 8 (07) :508-514
[9]   Enhancement of gene expression by polyamidoamine dendrimer conjugates with α-, β-, and γ-cyclodextrins [J].
Arima, H ;
Kihara, F ;
Hirayama, F ;
Uekama, K .
BIOCONJUGATE CHEMISTRY, 2001, 12 (04) :476-484
[10]  
Arteaga CL, 2001, J CLIN ONCOL, V19, p32S