Skip to main content
Presentation
Lipoplexes with pH-sensitive conformational switch for siRNA delivery
246th National Meeting and Exposition of American Chemical Society (ACS)
  • Shen Zhao, University of the Pacific
  • Yu Zheng, University of the Pacific
  • Xin Liu, University of the Pacific
  • Xin Guo, University of the Pacific
  • Vyacheslav V. Samoshin, University of the Pacific
  • Andreas H. Franz, University of the Pacific
Document Type
Poster
Organization
American Chemical Society (ACS)
Location
Indianapolis, IN
Conference Dates
September 8-12, 2013
Date of Presentation
9-8-2013
Abstract
siRNA represents a promising category of therapeutic agents for the treatment of viral and genetic diseases. However, successful gene knockdown by siRNA depends on its efficient delivery into target cells. Previously, we have reported pH-sensitive liposomes with conformational switch (Fliposomes) as a potential delivery system for small-molecule drugs and biomacromolecules. In this study, we prepared complexes of cationic Fliposomes and siRNA to transfect T47D-KBluc cells (human breast cancer), which stably express firefly luciferase. The cationic Fliposomes and their complexes with siRNA were prepared either with or without poly-L-glutamic acid (PG) as a stabilizer. Electrophoresis studies indicated that PG improved the stability of the Fliposome-siRNA complexes. Significantly more efficient knockdown of the luciferase activity was achieved by the Fliposome/siRNA complexes compared to liposome/siRNA complexes containing the common cationic lipid DOTAP. PG also enhanced the transfection efficiency of the complexes in T47D-KBluc cells. Two other mammalian cell lines expressing GFP (green fluorescent protein) were also investigated as potential cell lines to evaluate the efficiency of siRNA delivery by Fliposomes.
Citation Information
Shen Zhao, Yu Zheng, Xin Liu, Xin Guo, et al.. "Lipoplexes with pH-sensitive conformational switch for siRNA delivery" 246th National Meeting and Exposition of American Chemical Society (ACS) (2013)
Available at: http://works.bepress.com/xin-guo/43/