Superparamagnetic iron oxide nanoparticles-loaded chitosan-linoleic acid nanoparticles as an effective hepatocyte-targeted gene delivery system

被引:65
作者
Cheong, Sui-Jin [1 ,2 ,3 ]
Lee, Chang-Moon [1 ,2 ,3 ]
Kim, Se-Lim [1 ,2 ,3 ]
Jeong, Hwan-Jeong [1 ,2 ,3 ]
Kim, Eun-Mi [1 ,2 ,3 ]
Park, Eun-Hye [1 ,2 ,3 ]
Kim, Dong Wook [1 ,2 ,3 ]
Lim, Seok Tae [1 ,2 ,3 ]
Sohn, Myung-Hee [1 ,2 ,3 ]
机构
[1] Chonbuk Natl Univ, Dept Nucl Med, Med Sch & Hosp, Jeonju 561756, South Korea
[2] Chonbuk Natl Univ, Res Inst Clin Med, Med Sch & Hosp, Jeonju 561756, South Korea
[3] Chonbuk Natl Univ, Inst Med Sci, Med Sch & Hosp, Jeonju 561756, South Korea
关键词
Gene delivery; Superparamagnetic iron oxide; nanoparticles; Chitosan; Linoleic acid; Hepatocyte; Molecular imaging; PLASMID DNA; COMPLEXES; VECTORS;
D O I
10.1016/j.ijpharm.2009.01.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The goal of this study was to develop a gene delivery imaging system that targets hepatocytes to help diagnose and treat various liver diseases. To this end, we prepared superparamagnetic iron oxide nanoparticles (SPIO)-loaded with water-soluble chitosan (WSC)-linoleic acid (LA) nanoparticles (SCLNs) that formed gene complexes capable of localizing specifically to hepatocytes. We confirmed that Tc-99m-labeled SCLNs delivered into mice via intravenous injection accumulated mainly in the liver using nuclear and magnetic resonance imaging. SCLN/enhanced green fluorescence protein (pEGFP) complexes were also successfully formed and were characterized with a gel retardation assay. SCLN/pEGFP complexes were transfected into primary hepatocytes, where GFP expression was observed in the cytoplasm. In addition, the injection of the gene complexes into mice resulted in significantly increased expression of GFP in hepatocytes in vivo. Furthermore, gene silencing was effectively achieved by administration of gene complexes loaded with specific siRNAs. In conclusion, our results indicate that the SCLNs have the potential to be useful for hepatocyte-targeted imaging and effective gene delivery into hepatocytes. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 176
页数:8
相关论文
共 26 条
[1]   Effects of a new bioactive lipid-based drug carrier on cultured hepatic stellate cells and liver fibrosis in bile duct-ligated rats [J].
Adrian, Joanna E. ;
Poelstra, Klaas ;
Scherphof, Gerrit L. ;
Meijer, Dirk K. F. ;
van Loenen-Weemaes, Anne-miek ;
Reker-Smit, Catharina ;
Morselt, Henriette W. M. ;
Zwiers, Peter ;
Kamps, Jan A. A. M. .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 321 (02) :536-543
[2]   Chitosans for gene delivery [J].
Borchard, G .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 52 (02) :145-150
[3]   Iron oxide MR contrast agents for molecular and cellular imaging [J].
Bulte, JWM ;
Kraitchman, DL .
NMR IN BIOMEDICINE, 2004, 17 (07) :484-499
[4]   Non-viral gene delivery systems [J].
Davis, ME .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (02) :128-131
[5]   Chitosan-based vector/DNA complexes for gene delivery: Biophysical characteristics and transfection ability [J].
Erbacher, P ;
Zou, SM ;
Bettinger, T ;
Steffan, AM ;
Remy, JS .
PHARMACEUTICAL RESEARCH, 1998, 15 (09) :1332-1339
[6]   Targeting delivery of oligonucleotide and plasmid DNA to hepatocyte via galactosylated chitosan vector [J].
Gao, SY ;
Chen, JN ;
Dong, L ;
Ding, Z ;
Yang, YH ;
Zhang, JF .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 60 (03) :327-334
[7]   Nanoscale size effect of magnetic nanocrystals and their utilization for cancer diagnosis via magnetic resonance imaging [J].
Jun, YW ;
Huh, YM ;
Choi, JS ;
Lee, JH ;
Song, HT ;
Kim, S ;
Yoon, S ;
Kim, KS ;
Shin, JS ;
Suh, JS ;
Cheon, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (16) :5732-5733
[8]   Asialoglycoprotein-receptor-targeted hepatocyte imaging using 99mTc galactosylated chitosan [J].
Kim, Eun-Mi ;
Jeong, Hwan-Jeong ;
Kim, Se-Lim ;
Sohn, Myung-Hee ;
Nah, Jae-Woon ;
Bom, Hee-Seung ;
Park, In-Kyu ;
Cho, Chong-Su .
NUCLEAR MEDICINE AND BIOLOGY, 2006, 33 (04) :529-534
[9]   Linolenic acid-modified chitosan for formation of self-assembled nanoparticles [J].
Liu, CG ;
Desai, KGH ;
Chen, XG ;
Park, HJ .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (02) :437-441
[10]   Chitosan-DNA nanoparticles as non-viral vectors in gene therapy: strategies to improve transfection efficacy [J].
Mansouri, S ;
Lavigne, P ;
Corsi, K ;
Benderdour, M ;
Beaumont, E ;
Fernandes, JC .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 57 (01) :1-8