Gene Transfer into the Lung by Nanoparticle Dextran-Spermine/Plasmid DNA Complexes

被引:32
作者
Abdullah, Syahril [1 ,2 ]
Wendy-Yeo, Wai Yeng [1 ,2 ]
Hosseinkhani, Hossein [3 ,4 ]
Hosseinkhani, Mohsen [5 ]
Masrawa, Ehab [6 ]
Ramasamy, Rajesh [1 ,7 ]
Rosli, Rozita [1 ,2 ]
Rahman, Sabariah A. [1 ,7 ]
Domb, Abraham J. [6 ]
机构
[1] Univ Putra Malaysia, MAKNA Canc Res Lab, Inst Biosci, Upm Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Med Genet Lab, Fac Med & Hlth Sci, Upm Serdang 43400, Selangor, Malaysia
[3] MIT, Ctr Biomed Engn, Cambridge, MA 02139 USA
[4] Tokyo Womens Med Univ, Int Res Inst Integrated Med Sci IREIIMS, Tokyo 1628666, Japan
[5] Tufts Univ, Sch Med, Ctr Canc Syst Biol, Caritas St Elizabeths Med Ctr, Medford, MA 02135 USA
[6] Hebrew Univ Jerusalem, Sch Pharm, Hadassah Med Sch, Dept Med Chem & Nat Prod, IL-91120 Jerusalem, Israel
[7] Univ Putra Malaysia, Dept Pathol, Fac Med & Hlth Sci, Upm Serdang 43400, Selangor, Malaysia
来源
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY | 2010年
关键词
MESENCHYMAL STEM-CELLS; IN-VITRO; PLASMID DNA; TRANSGENE EXPRESSION; CATIONIZED DEXTRAN; NONVIRAL VECTORS; CYSTIC-FIBROSIS; DELIVERY; VIVO; EFFICIENT;
D O I
10.1155/2010/284840
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
A novel cationic polymer, dextran-spermine (D-SPM), has been found to mediate gene expression in a wide variety of cell lines and in vivo through systemic delivery. Here, we extended the observations by determining the optimal conditions for gene expression of D-SPM/plasmid DNA (D-SPM/pDNA) in cell lines and in the lungs of BALB/c mice via instillation delivery. In vitro studies showed that D-SPM could partially protect pDNA from degradation by nuclease and exhibited optimal gene transfer efficiency at D-SPM to pDNA weight-mixing ratio of 12. In the lungs of mice, the levels of gene expression generated by D-SPM/pDNA are highly dependent on the weight-mixing ratio of D-SPM to pDNA, amount of pDNA in the complex, and the assay time postdelivery. Readministration of the complex at day 1 following the first dosing showed no significant effect on the retention and duration of gene expression. The study also showed that there was a clear trend of increasing size of the complexes as the amount of pDNA was increased, where the sizes of the D-SPM/pDNA complexes were within the nanometer range.
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页数:10
相关论文
共 57 条
[21]   Enhanced ectopic bone formation using a combination of plasmid DNA impregnation into 3-D scaffold and bioreactor perfusion culture [J].
Hosseinkhani, H ;
Yamamoto, M ;
Inatsugu, Y ;
Hiraoka, Y ;
Inoue, S ;
Shimokawa, H ;
Tabata, Y .
BIOMATERIALS, 2006, 27 (08) :1387-1398
[22]   RETRACTED: Ultrasound enhances in vivo tumor expression of plasmid DNA by PEG-introduced cationized dextran (Retracted article. See vol. 232, pg. 269, 2016) [J].
Hosseinkhani, H ;
Tabata, Y .
JOURNAL OF CONTROLLED RELEASE, 2005, 108 (2-3) :540-556
[23]   Impregnation of plasmid DNA into three-dimensional scaffolds and medium perfusion enhance in vitro DNA expression of mesenchymal stem cells [J].
Hosseinkhani, H ;
Inatsugu, Y ;
Hiraoka, Y ;
Inoue, S ;
Shimokawa, H ;
Tabata, Y .
TISSUE ENGINEERING, 2005, 11 (9-10) :1459-1475
[24]   RETRACTED: Tumor targeting of gene expression through metal-coordinated conjugation with dextran (Retracted article. See vol. 232, pg. 266, 2016) [J].
Hosseinkhani, H ;
Aoyama, T ;
Ogawa, O ;
Tabata, Y .
JOURNAL OF CONTROLLED RELEASE, 2003, 88 (02) :297-312
[25]   DNA nanoparticles encapsulated in 3D tissue-engineered scaffolds enhance osteogenic differentiation of mesenchymal stem cells [J].
Hosseinkhani, Hossein ;
Hosseinkhani, Mohsen ;
Gabrielson, Nathan P. ;
Pack, Daniel W. ;
Khademhosseini, Ali ;
Kobayashi, Hisatoshi .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2008, 85A (01) :47-60
[26]   Combination of 3D tissue engineered scaffold and non-viral gene carrier enhance in vitro DNA expression of mesenchymal stem cells [J].
Hosseinkhani, Hossein ;
Azzam, Tony ;
Kobayashi, Hisatoshi ;
Hiraoka, Yosuke ;
Shimokawa, Hitoyata ;
Domb, Abraham J. ;
Tabata, Yasuhiko .
BIOMATERIALS, 2006, 27 (23) :4269-4278
[27]   Biodegradable Polymer-Metal Complexes for Gene and Drug Delivery [J].
Hosseinkhani, Hossein ;
Hosseinkhani, Mohsen .
CURRENT DRUG SAFETY, 2009, 4 (01) :79-83
[28]   Non-viral gene transfection technologies for genetic engineering of stem cells [J].
Jo, Jun-Ichiro ;
Tabata, Yasuhiko .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 68 (01) :90-104
[29]   Tumor-targeted gene delivery using poly(ethylene glycol)-modified gelatin nanoparticles:: In vitro and in vivo studies [J].
Kaul, G ;
Amiji, M .
PHARMACEUTICAL RESEARCH, 2005, 22 (06) :951-961
[30]   Design and gene delivery activity of modified polyethylenimines [J].
Kircheis, R ;
Wightman, L ;
Wagner, E .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 53 (03) :341-358