Chemically Programmed Polymers for Targeted DNA and siRNA Transfection

被引:27
作者
Salcher, Eveline Edith [1 ,2 ]
Wagner, Ernst [1 ,2 ]
机构
[1] Univ Munich, Dept Pharm, Ctr Syst Based Drug Res, D-81377 Munich, Germany
[2] Univ Munich, Ctr Nanosci CeNS, D-81377 Munich, Germany
来源
NUCLEIC ACID TRANSFECTION | 2010年 / 296卷
关键词
Bioresponsive; Cationic polymers; Chemical programming; DNA; siRNA; GENE DELIVERY VECTORS; BIOREDUCIBLE POLY(AMIDO AMINE)S; DNA/TRANSFERRIN-PEI COMPLEXES; GROWTH-FACTOR RECEPTOR; IN-VIVO; HIGHLY EFFICIENT; PLASMID DNA; LINEAR POLYETHYLENIMINE; ENHANCED TRANSFECTION; DRUG-DELIVERY;
D O I
10.1007/128_2010_69
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Plasmid DNA and siRNA have a large potential for use as therapeutic nucleic acids in medicine. The way to the target cell and its proper compartment is full of obstacles. Polymeric carriers help to overcome the encountered barriers. Cationic polymers can interact with the nucleic acid in a nondamaging way but still require optimization with regard to transfer efficiency and biocompatibility. Aiming at virus-like features, as viruses are the most efficient natural gene carriers, the design of bioresponsive polymers shows promising results regarding DNA and siRNA delivery. By specific chemical modifications dynamic structures are created, programmed to respond towards changing demands on the delivery pathway by cleavage of labile bonds or conformational changes, thus enhancing biocompatible gene delivery.
引用
收藏
页码:227 / 249
页数:23
相关论文
共 156 条
[1]   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
[2]   Gene silencing through RNA interference (RNAi) in vivo: Strategies based on the direct application of siRNAs [J].
Aigner, A .
JOURNAL OF BIOTECHNOLOGY, 2006, 124 (01) :12-25
[3]   Exploring polyethylenimine-mediated DNA transfection and the proton sponge hypothesis [J].
Akinc, A ;
Thomas, M ;
Klibanov, AM ;
Langer, R .
JOURNAL OF GENE MEDICINE, 2005, 7 (05) :657-663
[4]   Stimuli responsive polymers for biomedical applications [J].
Alarcón, CDH ;
Pennadam, S ;
Alexander, C .
CHEMICAL SOCIETY REVIEWS, 2005, 34 (03) :276-285
[5]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[6]   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
[7]   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
[8]   A biodegradable poly(ester amine) based on polycaprolactone and polyethylenimine as a gene carrier [J].
Arote, Rohidas ;
Kim, Tae-Hee ;
Kim, You-Kyoung ;
Hwang, Soon-Kyung ;
Jiang, Hu-Lin ;
Song, Ho-Hyun ;
Nah, Jae-Woon ;
Cho, Myung-Haing ;
Cho, Chong-Su .
BIOMATERIALS, 2007, 28 (04) :735-744
[9]   Progress towards in vivo use of siRNAs [J].
Behlke, MA .
MOLECULAR THERAPY, 2006, 13 (04) :644-670
[10]  
Berg K, 1999, CANCER RES, V59, P1180