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Theranostic nanoparticles based on bioreducible polyethylenimine-coated iron oxide for reduction-responsive gene delivery and magnetic resonance imaging
被引:40
|作者:
Li, Dan
[1
]
Tang, Xin
[2
]
Pulli, Benjamin
[1
]
Lin, Chao
[2
]
Zhao, Peng
[2
]
Cheng, Jian
[2
]
Lv, Zhongwei
[1
]
Yuan, Xueyu
[1
]
Luo, Qiong
[1
]
Cai, Haidong
[1
]
Ye, Meng
[1
]
机构:
[1] Tongji Univ, Dept Nucl Med, Shanghai Peoples Hosp 10, Sch Med, Shanghai 200092, Peoples R China
[2] Tongji Univ, Shanghai East Hosp, Inst Biomed Engn & Nanosci, Sch Med, Shanghai 200092, Peoples R China
来源:
INTERNATIONAL JOURNAL OF NANOMEDICINE
|
2014年
/
9卷
基金:
国家高技术研究发展计划(863计划);
关键词:
nanoparticles;
SSPEI;
hTERT;
disulfide;
RNA interference;
tumor;
MR imaging;
TELOMERASE REVERSE-TRANSCRIPTASE;
GROWTH IN-VITRO;
POLY(AMIDO AMINE)S;
POTENTIAL BARRIER;
SIRNA;
CANCER;
VECTOR;
DOXORUBICIN;
DRUG;
VIVO;
D O I:
10.2147/IJN.S61463
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Theranostic nanoparticles based on superparamagnetic iron oxide (SPIO) have a great promise for tumor diagnosis and gene therapy. However, the availability of theranostic nanoparticles with efficient gene transfection and minimal toxicity remains a big challenge. In this study, we construct an intelligent SPIO-based nanoparticle comprising a SPIO inner core and a disulfide-containing polyethylenimine (SSPEI) outer layer, which is referred to as a SSPEI-SPIO nanoparticle, for redox-triggered gene release in response to an intracellular reducing environment. We reveal that SSPEI-SPIO nanoparticles are capable of binding genes to form nano-complexes and mediating a facilitated gene release in the presence of dithiothreitol (5-20 mM), thereby leading to high transfection efficiency against different cancer cells. The SSPEI-SPIO nanoparticles are also able to deliver small interfering RNA (siRNA) for the silencing of human telomerase reverse transcriptase genes in HepG2 cells, causing their apoptosis and growth inhibition. Further, the nanoparticles are applicable as T2-negative contrast agents for magnetic resonance (MR) imaging of a tumor xenografted in a nude mouse. Importantly, SSPEI-SPIO nanoparticles have relatively low cytotoxicity in vitro at a high concentration of 100 mu g/mL. The results of this study demonstrate the utility of a disulfide-containing cationic polymer-decorated SPIO nanoparticle as highly potent and low-toxic theranostic nano-system for specific nucleic acid delivery inside cancer cells.
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页码:3347 / 3361
页数:15
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