4.7 Article

Efficient siRNA delivery using novel siRNA-loaded Bubble liposomes and ultrasound

期刊

INTERNATIONAL JOURNAL OF PHARMACEUTICS
卷 422, 期 1-2, 页码 504-509

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijpharm.2011.11.023

关键词

siRNA delivery; Ultrasound; Bubble liposomes

资金

  1. New Energy and Industrial Technology Development Organization (NEDO) of Japan [04A05010]
  2. Japan Society for the Promotion of Science [18650146, 20300179, 21790164]
  3. Grants-in-Aid for Scientific Research [21790164, 18650146] Funding Source: KAKEN

向作者/读者索取更多资源

Recently, we developed novel polyethyleneglycol (PEG)-modified liposomes (Bubble liposomes; BLs) entrapping an ultrasound (US) imaging gas and reported that the combination of BLs and US was useful for the delivery of siRNA directly into the cytoplasm. However, the results were obtained using a mixture of BLs and naked siRNA. With systemic injections, it is important to control the biodistribution of both BLs and siRNA. In addition, the delivery of siRNA is affected by nuclease degradation after intravenous administration. In this study, we prepared novel siRNA-loaded BLs (si-BLs) using a cationic lipid, 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP). We demonstrated that siRNA could be loaded onto BLs containing DOTAP and that siRNA-loaded BLs were stable in serum. A specific gene-silencing effect was also achieved by transfection with si-BLs. Thus, the combination of si-BLs with US exposure can be used for delivery of siRNA to a specific tissue via systemic injection. (C) 2011 Elsevier B. V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据