Glutathione-Responsive Multilayer Coated Gold Nanoparticles for Targeted Gene Delivery

被引:28
作者
Yu, Feifei [1 ]
Huang, Jingbin [1 ]
Yu, Yuan [1 ]
Lu, Ying [1 ]
Chen, Yan [1 ]
Zhang, He [1 ]
Zhou, Guichen [3 ]
Sun, Zhiguo [1 ]
Liu, Junjie [1 ]
Sung, Duxin [2 ]
Zhang, Guoqing [3 ]
Zou, Hao [1 ]
Zhong, Yanqiang [1 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Dept Pharmaceut Sci, Shanghai 200433, Peoples R China
[2] Univ Michigan, Sch Pharm, Dept Pharmaceut Sci, Ann Arbor, MI 48109 USA
[3] Eastern Hepatobiliaty Surg Hosp, Dept Pharm, Shanghai 200438, Peoples R China
关键词
Gold Nanoparticles; pTAT; Hyaluronic Acid; Glutathione-Responsive; TAT-PEPTIDE; DRUG-DELIVERY; DNA; VECTORS; BIODISTRIBUTION; POLYETHYLENIMINE; AGENTS; LIVER; SIRNA;
D O I
10.1166/jbn.2016.2177
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Efficient gene release after intracellular uptake is very important for non-viral gene delivery systems. To construct a glutathione-responsive gene delivery system, we developed gold-cysteamine (AuCM)/plasmid DNA (pDNA)/poly TAT (pTAT)/hyaluronic acid (HA) nanocomplexes (AuCM/pDNA/pTAT/HA) in this study. The AuCM/pDNA/pTAT/HA nanocomplexes possessed a small size less than 200 nm and negative zeta potential of -17 +/- 4 mV. The multilayer structure was verified by UV-Vis spectra, surface charges, dynamic light scattering. Morphology was observed by transmission electron microscope. The AuCM/pDNA/pTAT/HA nanocomplexes could completely protect pDNA against enzymatic degradation. These nanocomplexes showed effective cellular uptake in CD44 receptors over-expressed HepG 2 cells in a HA/CD44 interaction dependent manner. Moreover, transfection efficacy was significantly enhanced in AuCM/pDNA/pTAT/HA treated HepG 2 cells compared with AuCM/pDNA/pTAT, and was further enhanced in the presence of GSH, indicating that AuCM/pDNA/pTAT/HA was glutathione-responsive. Biodistribution revealed that AuCM/pDNA/pTAT/HA nanocomplexes mainly accumulated in liver. In conclusion, AuCM/pDNA/pTAT/HA nanocomplexes may serve as glutathione-responsive gene carriers for actively targeting gene delivery to CD44 receptors over-expressed liver cancers.
引用
收藏
页码:503 / 515
页数:13
相关论文
共 37 条
[1]   Biodistribution of gold nanoparticles and gene expression changes in the liver and spleen after intravenous administration in rats [J].
Balasubramanian, Suresh K. ;
Jittiwat, Jinattal ;
Manikandan, Jayapal ;
Ong, Choon-Nam ;
Yu, Liya E. ;
Ong, Wei-Yi .
BIOMATERIALS, 2010, 31 (08) :2034-2042
[2]   Disassembly of layer-by-layer films of plasmid DNA and reducible TAT polypeptide [J].
Blacklock, Jenifer ;
Handa, Hitesh ;
Manickam, Devika Soundara ;
Mao, Guangzhao ;
Mukhopadhyay, Ashis ;
Oupicky, David .
BIOMATERIALS, 2007, 28 (01) :117-124
[3]   Addition of a C-terminal cysteine improves the anti-herpes simplex virus activity of a peptide containing the human immunodeficiency virus type 1 TAT protein transduction domain [J].
Bultmann, Hermann ;
Teuton, Jeremy ;
Brandt, Curtis R. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (05) :1596-1607
[4]   In situ preparation of gold nanoparticle-loaded lysozyme-dextran nanogels and applications for cell imaging and drug delivery [J].
Cai, Huanxin ;
Yao, Ping .
NANOSCALE, 2013, 5 (07) :2892-2900
[5]   A pH-responsive cyclodextrin-based hybrid nanosystem as a nonviral vector for gene delivery [J].
Chen, Huaping ;
Liu, Xueping ;
Dou, Yin ;
He, Binfeng ;
Liu, Li ;
Wei, Zhenghua ;
Li, Jin ;
Wang, Changzheng ;
Mao, Chengde ;
Zhang, Jianxiang ;
Wang, Guansong .
BIOMATERIALS, 2013, 34 (16) :4159-4172
[6]   Glutathione-responsive nano-vehicles as a promising platform for targeted intracellular drug and gene delivery [J].
Cheng, Ru ;
Feng, Fang ;
Meng, Fenghua ;
Deng, Chao ;
Feijen, Jan ;
Zhong, Zhiyuan .
JOURNAL OF CONTROLLED RELEASE, 2011, 152 (01) :2-12
[7]   Stabilization of Polymer-Hydrogel Capsules via Thiol-Disulfide Exchange [J].
Chong, Siow-Feng ;
Chandrawati, Rona ;
Staedler, Brigitte ;
Park, Jeongju ;
Cho, Jinhan ;
Wang, Yajun ;
Jia, Zhongfan ;
Bulmus, Volga ;
Davis, Thomas P. ;
Zelikin, Alexander N. ;
Caruso, Frank .
SMALL, 2009, 5 (22) :2601-2610
[8]   Particle size-dependent organ distribution of gold nanoparticles after intravenous administration [J].
De Jong, Wim H. ;
Hagens, Werner I. ;
Krystek, Petra ;
Burger, Marina C. ;
Sips, Adrienne J. A. M. ;
Geertsma, Robert E. .
BIOMATERIALS, 2008, 29 (12) :1912-1919
[9]   Gold nanoparticle platforms as drug and biomacromolecule delivery systems [J].
Duncan, Bradley ;
Kim, Chaekyu ;
Rotello, Vincent M. .
JOURNAL OF CONTROLLED RELEASE, 2010, 148 (01) :122-127
[10]   Layer-by-Layer Assembled Gold Nanoparticles for siRNA Delivery [J].
Elbakry, Asmaa ;
Zaky, Alaa ;
Liebkl, Renate ;
Rachel, Reinhard ;
Goepferich, Achim ;
Breunig, Miriam .
NANO LETTERS, 2009, 9 (05) :2059-2064