Temperature-controlled properties of DNA complexes with poly(ethylenimine)-graft-poly(N-isopropylacrylamide)

被引:94
作者
Bisht, HS [1 ]
Manickam, DS [1 ]
You, YZ [1 ]
Oupicky, D [1 ]
机构
[1] Wayne State Univ, Dept Pharmaceut Sci, Detroit, MI 48202 USA
关键词
D O I
10.1021/bm0509927
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
End-functionalized poly(N-isopropylacrylamide) (PNIPA) was synthesized by living free radical polymerization and conventional free radical polymerization and was used to prepare graft copolymers with poly(ethylenimine) (PEI). The copolymers exhibited lower critical solution temperature (LCST) behavior between 30 and 32 degrees C and formed complexes with plasmid DNA. The LCST of the copolymers in the DNA complexes increased slightly to similar to 34-35 degrees C. Cytotoxicity of the copolymers was evaluated by measuring lactate dehydrogenase (LDH) release from cells. The copolymers exhibited temperature-dependent toxicity, with higher levels of LDH release observed at temperatures above the LCST. Cellular uptake and transfection activity of the DNA complexes with the PEI-g-PNIPA copolymers were lower than those of the control PEI/DNA complexes at temperature below the LCST but increased to the PEI/DNA levels at temperatures above the LCST.
引用
收藏
页码:1169 / 1178
页数:10
相关论文
共 46 条
[1]   Stimuli responsive polymers for biomedical applications [J].
Alarcón, CDH ;
Pennadam, S ;
Alexander, C .
CHEMICAL SOCIETY REVIEWS, 2005, 34 (03) :276-285
[2]   pH-controlled association of PEG-containing terpolymers of N-isopropylacrylamide and 1-vinylimidazole [J].
Bisht, HS ;
Wan, L ;
Mao, GZ ;
Oupicky, D .
POLYMER, 2005, 46 (19) :7945-7952
[3]   Different strategies for formation of PEGylated EGF-conjugated PEI/DNA complexes for targeted gene delivery [J].
Blessing, T ;
Kursa, M ;
Holzhauser, R ;
Kircheis, R ;
Wagner, E .
BIOCONJUGATE CHEMISTRY, 2001, 12 (04) :529-537
[4]   Purification of polyethylenimine polyplexes highlights the role of free polycations in gene transfer [J].
Boeckle, S ;
von Gersdorff, K ;
van der Piepen, S ;
Culmsee, C ;
Wagner, E ;
Ogris, M .
JOURNAL OF GENE MEDICINE, 2004, 6 (10) :1102-1111
[5]   Recognition of DNA topology in reactions between plasmid DNA and cationic copolymers [J].
Bronich, TK ;
Nguyen, HK ;
Eisenberg, A ;
Kabanov, AV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (35) :8339-8343
[6]   Facile, controlled, room-temperature RAFT polymerization of N-isopropylacrylamide [J].
Convertine, AJ ;
Ayres, N ;
Scales, CW ;
Lowe, AB ;
McCormick, CL .
BIOMACROMOLECULES, 2004, 5 (04) :1177-1180
[7]   Molecular weight and functional end group control by RAFT polymerization of a bisubstituted acrylamide derivative [J].
D'Agosto, F ;
Hughes, R ;
Charreyre, MT ;
Pichot, C ;
Gilbert, RG .
MACROMOLECULES, 2003, 36 (03) :621-629
[8]   A novel non-viral vector for DNA delivery based on low molecular weight, branched polyethylenimine:: Effect of molecular weight on transfection efficiency and cytotoxicity [J].
Fischer, D ;
Bieber, T ;
Li, YX ;
Elsässer, HP ;
Kissel, T .
PHARMACEUTICAL RESEARCH, 1999, 16 (08) :1273-1279
[9]   In vitro cytotoxicity testing of polycations: influence of polymer structure on cell viability and hemolysis. [J].
Fischer, D ;
Li, YX ;
Ahlemeyer, B ;
Krieglstein, J ;
Kissel, T .
BIOMATERIALS, 2003, 24 (07) :1121-1131
[10]   Poly(ethylenimine)-mediated gene delivery affects endothelial cell function and viability [J].
Godbey, WT ;
Wu, KK ;
Mikos, AG .
BIOMATERIALS, 2001, 22 (05) :471-480