Chitosan-graft-polyethylenimine with improved properties as a potential gene vector

被引:49
作者
Li, Zong-Tao [1 ]
Guo, Jia [1 ]
Zhang, Jin-Song [2 ]
Zhao, Yan-Ping [1 ]
Lv, Lu [1 ]
Ding, Cing [1 ]
Zhang, Xian-Zheng [3 ,4 ]
机构
[1] Wuhan Univ, Coll Pharm, Wuhan 430072, Peoples R China
[2] Wuhan Inst Technol, Sch Chem Engn & Pharm, Wuhan 430073, Peoples R China
[3] Wuhan Univ, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Peoples R China
[4] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
关键词
Chitosan-graft-polyethylenimine; Disulfide linkage; Gene delivery; MOLECULAR-WEIGHT POLYETHYLENIMINE; TRANSFECTION EFFICIENCY; DNA DELIVERY; IN-VITRO; NONVIRAL VECTOR; DESIGN; DERIVATIVES; COMPLEXES; POLYMERS; CARRIER;
D O I
10.1016/j.carbpol.2009.11.021
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel chitosan-graft-polyethylenimine (CHI-g-PEI) copolymer with biocleavable disulfide linkages between chitosan chains and PEI grafts was synthesized, characterized, and examined as a potential nonviral gene vector. The chemical structure of the obtained product was characterized by (1)H NMR, FTIR and Raman spectroscopy, respectively. Agarose gel retardation assay, dynamic light scattering, and scanning electron microscopy experiments revealed that CHI-g-PEI had a good ability of condensing plasmid DNA into spherical nanoparticles in the size range of 200-300 nm. In the imitative physiological environment the polymer/pDNA complexes are relatively stable, meanwhile, an efficient release of pDNA was detected in the presence of 25 mM DTT, mimicking the intracellular reductive environment. These results show that the bioreducible CHI-g-PEI copolymer, thus obtained, can be used as a promising nonviral gene carrier due to its excellent properties. Published by Elsevier Ltd.
引用
收藏
页码:254 / 259
页数:6
相关论文
共 31 条
[1]   pH-sensitive cationic polymer gene delivery vehicle:: N-Ac-poly(L-histidine)-graft-poly(L-lysine) comb shaped polymer [J].
Benns, JM ;
Choi, JS ;
Mahato, RI ;
Park, JS ;
Kim, SW .
BIOCONJUGATE CHEMISTRY, 2000, 11 (05) :637-645
[2]   Optimization of factors influencing the transfection efficiency of folate-PEG-folate-graft-polyethylenimine [J].
Benns, JM ;
Mahato, RI ;
Kim, SW .
JOURNAL OF CONTROLLED RELEASE, 2002, 79 (1-3) :255-269
[3]  
GILBERT HF, 1995, METHOD ENZYMOL, V251, P8, DOI 10.1016/0076-6879(95)51107-5
[4]   Tracking the intracellular path of poly(ethylenimine)/DNA complexes for gene delivery [J].
Godbey, WT ;
Wu, KK ;
Mikos, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :5177-5181
[5]   Toxicity Evaluation for Safe Use of Nanomaterials: Recent Achievements and Technical Challenges [J].
Hussain, Saber M. ;
Braydich-Stolle, Laura K. ;
Schrand, Amanda M. ;
Murdock, Richard C. ;
Yu, Kyung O. ;
Mattie, David M. ;
Schlager, John J. ;
Terrones, Mouricio .
ADVANCED MATERIALS, 2009, 21 (16) :1549-1559
[6]   Molecular design of functional polymers for gene therapy [J].
Jeong, Ji Hoon ;
Kim, Sung Wan ;
Park, Tae Gwan .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (11) :1239-1274
[7]   Chitosan-graft-polyethylenimine as a gene carrier [J].
Jiang, Hu-Lin ;
Kim, You-Kyoung ;
Arote, Rohidas ;
Nah, Jae-Woon ;
Cho, Myung-Haing ;
Choi, Yun-Jaie ;
Akaike, Toshihiro ;
Cho, Chong-Su .
JOURNAL OF CONTROLLED RELEASE, 2007, 117 (02) :273-280
[8]   The effect of the degree of chitosan deacetylation on the efficiency of gene transfection [J].
Kiang, T ;
Wen, H ;
Lim, HW ;
Leong, KW .
BIOMATERIALS, 2004, 25 (22) :5293-5301
[9]   Structural characteristics of size-controlled self-aggregates of deoxycholic acid-modified chitosan and their application as a DNA delivery carrier [J].
Kim, YH ;
Gihm, SH ;
Park, CR ;
Lee, KY ;
Kim, TW ;
Kwon, IC ;
Chung, H ;
Jeong, SY .
BIOCONJUGATE CHEMISTRY, 2001, 12 (06) :932-938
[10]   Design and gene delivery activity of modified polyethylenimines [J].
Kircheis, R ;
Wightman, L ;
Wagner, E .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 53 (03) :341-358