pH-Sensitive siRNA Nanovector for Targeted Gene Silencing and Cytotoxic Effect in Cancer Cells

被引:100
|
作者
Mok, Hyejung [1 ]
Veiseh, Omid [1 ]
Fang, Chen [1 ]
Kievit, Forrest M. [1 ]
Wang, Freddy Y. [1 ]
Park, James O. [2 ]
Zhang, Miqin [1 ,3 ,4 ]
机构
[1] Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA
[2] Univ Washington, Dept Surg, Seattle, WA 98195 USA
[3] Univ Washington, Dept Radiol, Seattle, WA 98195 USA
[4] Univ Washington, Dept Neurol Surg, Seattle, WA 98195 USA
关键词
siRNA; iron oxide nanoparticle; cytotoxicity; pH-sensitive; cancer; nanotechnology; IRON-OXIDE NANOPARTICLES; IN-VITRO; INTRACELLULAR DELIVERY; MAGNETIC NANOPARTICLES; GOLD NANOPARTICLES; QUANTUM-DOT; ACIDIC PH; TUMOR PH; TRANSFECTION; RNA;
D O I
10.1021/mp100221h
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A small interfering RNA (siRNA) nanovector with dual targeting specificity and dual therapeutic effect is developed for targeted cancer imaging and therapy. The nanovector is composed of an iron oxide magnetic nanoparticle core coated with three different functional molecules: polyethyleneimine (PEI), siRNA, and chlorotoxin (CTX). The primary amine group of PEI is blocked with citraconic anhydride that is removable at acidic conditions, not only to increase its biocompatibility at physiological conditions but also to elicit a pH-sensitive cytotoxic effect in the acidic tumor microenvironment. The PEI is covalently immobilized on the nanovector via a disulfide linkage that is cleavable after cellular internalization of the nanovector. CTX as a tumor-specific targeting ligand and siRNA as a therapeutic payload are conjugated on the nanovector via a flexible and hydrophilic PEG linker for targeted gene silencing in cancer cells. With a size of similar to 60 nm, the nanovector exhibits long-term stability and good magnetic property for magnetic resonance imaging. The multifunctional nanovector exhibits both significant cytotoxic and gene silencing effects at acidic pH conditions for C6 glioma cells, but not at physiological pH conditions. Our results suggest that this nanovector system could be safely used as a potential therapeutic agent for targeted treatment of glioma as well as other cancers.
引用
收藏
页码:1930 / 1939
页数:10
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