Stimuli-responsive siRNA carriers for efficient gene silencing in tumors via systemic delivery

被引:11
|
作者
Shim, Min Suk [1 ]
Chang, Seong-Sil [2 ]
Kwon, Young Jik [3 ,4 ,5 ,6 ]
机构
[1] Incheon Natl Univ, Div Bioengn, Inchon 406772, South Korea
[2] Eulji Univ Hosp, Dept Occupat & Environm Med, Taejon, South Korea
[3] Univ Calif Irvine, Dept Pharmaceut Sci, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Chem Engn & Mat Sci, Irvine, CA 92697 USA
[5] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[6] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
关键词
RNA INTERFERENCE; BREAST-CANCER; MESSENGER-RNA; BLOOD; CELLS; POLYETHYLENIMINE; COMPLEXES; DNA;
D O I
10.1039/c3bm60187k
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Development of efficient carriers for small interfering RNA (siRNA) delivery and validation tools for assessing in vivo RNA interference (RNAi) efficiency is crucial to advance RNAi-based therapeutics to the clinic. Here, acid-degradable ketalized linear polyethylenimine (KL-PEI) designed for efficient, stimuli-responsive, and biocompatible siRNA delivery was used to complex with GFP-silencing siRNA (GFP siRNA) for in vivo RNAi. The in vivo gene silencing efficiency of GFP siRNA/KL-PEI polyplexes was evaluated at mRNA, protein, and histological levels using a mouse bearing a GFP-expressing tumor. Intravenously injected GFP siRNA/KL-PEI polyplexes significantly reduced GFP expression in tumors and whole blood of mice, depending on the dosage of GFP siRNA and the time course. Average GFP mRNA levels in the tumors of siRNA/KL-PEI polyplex-injected mice were also reduced. The described siRNA carriers and RNAi validation methodologies in this study may provide insightful clues for the development of RNAi-based therapeutics and preclinical trials.
引用
收藏
页码:35 / 40
页数:6
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