Stability and cellular uptake of polymerized siRNA (poly-siRNA)/polyethylenimine (PEI) complexes for efficient gene silencing

Seung Young Lee, Myung Sook Huh, Seulki Lee, So Jin Lee, Hyunjin Chung, Jae Hyung Park, Yu Kyoung Oh, Kuiwon Choi, Kwangmeyung Kim, Ick Chan Kwon

Research output: Contribution to journalArticlepeer-review

166 Citations (Scopus)


Small interfering RNA (siRNA) is a promising biological strategy for treatment of diverse diseases, but the therapeutic application of siRNA has been limited by its instability and poor cellular uptake efficiency. Although the development of various gene delivery systems has increased the siRNA delivery efficiency, many problems still remain to be resolved before the clinical application of siRNA. In this study, we suggest reducible polymerized siRNA a possible solution for low delivery efficiency of siRNA. Dithiol-modified red fluorescent protein (RFP) siRNAs at the 5'-ends of both sense and anti-sense strands were disulfide-polymerized. Polymerized siRNA (poly-siRNA) was composed of 30% oligomeric siRNA (50~300. bps) and 66% polymeric siRNA (above ~ 300. bps) as fractions, and was reducible in reducing solution through disulfide bond cleavage. Poly-siRNA formed more condensed and nano-sized complexes with low molecular weight polyethylenimine (PEI) by strong electrostatic interaction based on the higher charge density of poly-siRNA, compared with siRNA (mono-siRNA). The compact poly-siRNA/PEI complexes prevented the loss and degradation of siRNA from a polyanion competitor and RNases in serum. Furthermore, poly-siRNA/PEI complexes exhibited superior intracellular uptake by murine melanoma cells (B16F10), and was accompanied with RFP gene silencing efficiency of about 80%, compared to untreated cells. These results sufficiently support that strong polyanionic and reducible poly-siRNA can be utilized as a novel powerful therapeutic strategy for human diseases.

Original languageEnglish
Pages (from-to)339-346
Number of pages8
JournalJournal of Controlled Release
Issue number3
Publication statusPublished - 2010 Feb

Bibliographical note

Funding Information:
This work was financially supported by the Real-Time Molecular Imaging Project, Pioneer Research Program (2009-0081523), Fusion Technology Project (2009-0081876), and Global Research Laboratory Project of MEST and by a grant to the Intramural Research Program of the KIST , and by a grant ( A062254 ) of the Korea Health 21 R&D Project .


  • Electrostatic complexes
  • Gene silencing
  • Polyethylenimine
  • Polymerized siRNA
  • SiRNA

ASJC Scopus subject areas

  • Pharmaceutical Science


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