Mechanistic studies on aggregation of polyethylenimine-DNA complexes and its prevention

被引:64
作者
Sharma, VK
Thomas, M
Klibanov, AM [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
[2] MIT, Div Biol Engn, Cambridge, MA 02139 USA
关键词
nonviral gene delivery; plasmid DNA; polyethylenimine; aggregation; surfactants; stabilization;
D O I
10.1002/bit.20444
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aggregation of polyethylenimine (PEI)-DNA complexes severely undermines their utility for gene delivery into mammalian cells. Herein we undertook to elucidate the mechanism of this deleterious phenomenon and to develop rational strategies for its prevention. The effect of temperature, surfactants, complex concentration, ionic strength, viscosity, and pH on the time course of this aggregation was systematically examined. The aggregation process was completely inhibited by 2.5% polyoxyethylene (100) stearate (POES) and to a lesser degree by other nonionic surfactants. Importantly, POES preserved the transfection efficiency of the complexes without inducing toxicity. The aggregation was also reduced by lowering the temperature and pH, diluting the complexes, and increasing the solution viscosity. It is concluded that PEI-DNA complexes aggregate primarily due to hydrophobic interactions, while electrostatic attractions play little role. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:614 / 620
页数:7
相关论文
共 36 条
[1]   REPORTER GENES - APPLICATION TO THE STUDY OF MAMMALIAN GENE-TRANSCRIPTION [J].
ALAM, J ;
COOK, JL .
ANALYTICAL BIOCHEMISTRY, 1990, 188 (02) :245-254
[2]  
Anchordoquy TJ, 2000, J PHARM SCI, V89, P289, DOI 10.1002/(SICI)1520-6017(200003)89:3<289::AID-JPS1>3.3.CO
[3]  
2-E
[4]   Tween protects recombinant human growth hormone against agitation-induced damage via hydrophobic interactions [J].
Bam, NB ;
Cleland, JL ;
Yang, J ;
Manning, MC ;
Carpenter, JF ;
Kelley, RF ;
Randolph, JW .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (12) :1554-1559
[5]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[6]   Effect of size and serum proteins on transfection efficiency of poly((2-dimethylamino)ethyl methacrylate)-plasmid nanoparticles [J].
Cherng, JY ;
vandeWetering, P ;
Talsma, H ;
Crommelin, DJA ;
Hennink, WE .
PHARMACEUTICAL RESEARCH, 1996, 13 (07) :1038-1042
[7]   Non-viral gene delivery systems [J].
Davis, ME .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (02) :128-131
[8]   Cationic polymer based gene delivery systems [J].
De Smedt, SC ;
Demeester, J ;
Hennink, WE .
PHARMACEUTICAL RESEARCH, 2000, 17 (02) :113-126
[9]   Partial acetylation of polyethylenimine enhances in vitro gene delivery [J].
Forrest, ML ;
Meister, GE ;
Koerber, JT ;
Pack, DW .
PHARMACEUTICAL RESEARCH, 2004, 21 (02) :365-371
[10]   Size, diffusibility and transfection performance of linear PEI/DNA complexes in the mouse central nervous system [J].
Goula, D ;
Remy, JS ;
Erbacher, P ;
Wasowicz, M ;
Levi, G ;
Abdallah, B ;
Demeneix, BA .
GENE THERAPY, 1998, 5 (05) :712-717