Octaarginine-modified multifunctional envelope-type nano device for siRNA

被引:172
作者
Nakamura, Yoshio
Kogure, Kentaro
Futaki, Shiroh
Harashima, Hideyoshi
机构
[1] Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[2] Kyoto Univ, Inst Chem Res, Kyoto 6110011, Japan
关键词
siRNA; non-viral delivery system; liposomes; octaarginine; multifunctional envelope-type nano device;
D O I
10.1016/j.jconrel.2007.03.010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The multifunctional envelope-type nano device (MEND) is a novel non-viral gene delivery system for plasmid DNA (pDNA) and oligodeoxynucleotides (ODN). We showed previously that octaarginine-modified MEND (R8-MEND) produces a high transfection activity without cytotoxicity via macropinocytosis and efficient release of a condensed DNA core to the cytosol. In the present study, we succeeded in developing an efficient method for packaging siRNA into the R8-MEND, and its silencing effect was compared with that of transfection reagent TransIT-TKO. A polycation able to condense siRNA was screened for by measuring the size and zeta-potential of complexes formed between siRNA and the polycations poly-l-lysine (PLL), stearyl octaarginine (STR-R8) and protamine. Only STR-R8 was able to condense siRNA to form nano particles (<100 nm), whereas all three polycations were able to condense pDNA or ODN. The siRNA packaged in R8-MEND inhibited luciferase activity by more than 80% in HeLa cells stably expressing luciferase. Much amount of siRNA was internalized into the cells as R8-MEND, and siRNA was effectively released from lipid envelope of MEND to cytoplasm near the nucleus. Consequently, R8-MEND can deliver condensed siRNA into cells to produce an efficient and persistent silencing effect with minimum cytotoxicity. (c) 2007 Published by Elsevier B.V.
引用
收藏
页码:360 / 367
页数:8
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