253
Views
11
CrossRef citations to date
0
Altmetric
Research Article

Development of novel nucleic acid-loaded Bubble liposomes using cholesterol-conjugated siRNA

, , , , , , & show all
Pages 830-836 | Received 20 Feb 2011, Accepted 17 Apr 2011, Published online: 13 Jun 2011
 

Abstract

Recently, we developed polyethyleneglycol (PEG)-modified liposomes (Bubble liposomes; BLs) entrapping ultrasound (US) gas and reported that the combination of BLs and US exposure was an effective tool for the delivery of siRNA directly into cells and US-exposed tissues within a short period; 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 and rapid removal from the circulation after intravenous administration. In this study, we attempted to prepare novel siRNA-loaded BLs (chol-si-BLs) using cholesterol-conjugated siRNA (chol-siRNA). We demonstrated that chol-siRNA could be loaded into BLs, leading to the stability of siRNA even in the presence of an RNase. The specific gene-silencing effect was also achieved by transfection with chol-si-BLs and US. Thus, the combination of chol-si-BLs with US exposure is expected to deliver siRNA into a specific tissue via systemic injection.

Acknowledgements

The authors are grateful to Prof. Katsuro Tachibana (Department of Anatomy, School of Medicine, Fukuoka University) for technical advice regarding the induction of cavitation with US, and to Mr. Yasuhiko Hayakawa and Mr. Kosho Suzuki (NEPA GENE Co., Ltd.) for technical advice regarding US exposure.

Declaration of interest

This study was supported by a Grant for Industrial Technology Research (04A05010) from the New Energy and Industrial Technology Development Organization (NEDO) of Japan, a Grant-in-aid for Scientific Research (B) (20300179) from the Japan Society for the Promotion of Science, a Grant-in-aid for Scientific Research (B) (19300185) from the Japan Society for the Promotion of Science, and a Grant-in-aid for Young Scientists (B) (21790164) from the Japan Society for the Promotion of Science. Kazuo Maruyama acknowledges the Program for Promotion of Fundamental Studies (Project ID: 10–23) in Health Sciences of the National Institute of Biomedical Innovation (NIBIO).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.