Gene delivery in vitro and in vivo from bioreducible multilayered polyelectrolyte films of plasmid DNA

被引:113
作者
Blacklock, Jenifer [1 ,2 ]
You, Ye-Zi [1 ]
Zhou, Qing-Hui [1 ]
Mao, Guangzhao [3 ]
Oupicky, David [1 ]
机构
[1] Wayne State Univ, Dept Pharmaceut Sci, Detroit, MI 48202 USA
[2] Wayne State Univ, Dept Biomed Engn, Detroit, MI 48202 USA
[3] Wayne State Univ, Dept Chem Engn & Mat Sci, Detroit, MI 48202 USA
基金
美国国家卫生研究院;
关键词
Layer-by-layer; LBL; DNA; Polyelectrolyte films; In vivo transfection; PROTEIN DISULFIDE-ISOMERASE; CELL-SURFACE; THIN-FILMS; RELEASE; TRANSFECTION; COMPLEXES; BIOMATERIALS; SCAFFOLDS; LINKAGES; POLYMERS;
D O I
10.1016/j.biomaterials.2008.10.012
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Layer-by-layer (LbL) films were assembled on flexible stainless steel substrate using plasmid DNA and reducible hyperbranched poly(amido amine) (RHB) polycation. The films were characterized by XPS and their disassembly in reducing conditions confirmed by ellipsometry. Fibroblast and smooth muscle cell attachment and proliferation on DNA/RHB films were indistinguishable from those on control DNA/poly(ethylenimine) (PEI) films. In vitro transfection activity was evaluated using reporter plasmids encoding for secreted alkaline phosphatase (SEAP) and green fluorescent protein (GFP). DNA/RHB films showed higher and longer lasting transfection activity than control DNA/PEI films using SEAP plasmid. It was revealed through the use of GFP plasmid that DNA/RHB films transfected almost the entire cell population growing on the films. In vivo transfection activity was evaluated by subcutaneously implanting a stainless steel substrate coated with the DNA/RHB films containing SEAP plasmid DNA and measuring the levels of SEAP secreted into the blood circulation of rats. It was found that the plasma levels of SEAP peaked at similar to 160 ng SEAP/mL five days post-implantation. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:939 / 950
页数:12
相关论文
共 52 条
[1]
Biological responses to materials [J].
Anderson, JM .
ANNUAL REVIEW OF MATERIALS RESEARCH, 2001, 31 :81-110
[2]
Gene delivery through cell culture substrate adsorbed DNA complexes [J].
Bengali, Z ;
Pannier, AK ;
Segura, T ;
Anderson, BC ;
Jang, JH ;
Mustoe, TA ;
Shea, LD .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 90 (03) :290-302
[3]
Blackhurst DM, 2007, S AFR J ENOL VITIC, V28, P11
[4]
ZETA-POTENTIAL MEASUREMENTS ON PASSIVE METALS [J].
BOULANGEPETERMANN, L ;
DOREN, A ;
BAROUX, B ;
BELLONFONTAINE, MN .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1995, 171 (01) :179-186
[5]
Chastain M, 2001, J PHARM SCI, V90, P474, DOI 10.1002/1520-6017(200104)90:4<474::AID-JPS1005>3.0.CO
[6]
2-6
[7]
Reducible poly(amido ethylenimine)s designed for triggered intracellular gene delivery [J].
Christensen, Lane V. ;
Chang, Chien-Wen ;
Kim, Won Jong ;
Kim, Sung Wan ;
Zhong, Zhiyuan ;
Lin, Chao ;
Engbersen, Johan F. J. ;
Feijen, Jan .
BIOCONJUGATE CHEMISTRY, 2006, 17 (05) :1233-1240
[8]
Surface engineered and drug releasing pre-fabricated scaffolds for tissue engineering [J].
Chung, Hyun Jung ;
Park, Tae Gwan .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (4-5) :249-262
[9]
De Geest BG, 2007, CHEM SOC REV, V36, P636, DOI 10.1039/b600460c
[10]
Matrices and scaffolds for DNA delivery in tissue engineering [J].
De Laporte, Laura ;
Shea, Lonnie D. .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (4-5) :292-307