2007年6月
Octaarginine-modified multifunctional envelope-type nano device for siRNA
JOURNAL OF CONTROLLED RELEASE
- ,
- ,
- ,
- 巻
- 119
- 号
- 3
- 開始ページ
- 360
- 終了ページ
- 367
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1016/j.jconrel.2007.03.010
- 出版者・発行元
- ELSEVIER SCIENCE BV
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.
- リンク情報
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- DOI
- https://doi.org/10.1016/j.jconrel.2007.03.010
- J-GLOBAL
- https://jglobal.jst.go.jp/detail?JGLOBAL_ID=201102262048511117
- PubMed
- https://www.ncbi.nlm.nih.gov/pubmed/17478000
- Web of Science
- https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000247519900012&DestApp=WOS_CPL
- ID情報
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- DOI : 10.1016/j.jconrel.2007.03.010
- ISSN : 0168-3659
- J-Global ID : 201102262048511117
- PubMed ID : 17478000
- Web of Science ID : WOS:000247519900012