Penetration and efficacy of VEGF siRNA using polyelectrolyte complex micelles in a human solid tumor model in-vitro

Ahmed M. Al-Abd, Soo Hyeon Lee, Sun Hwa Kim, Jung Ho Cha, Tae Gwan Park, Seung Jin Lee, Hyo Jeong Kuh

Research output: Contribution to journalArticlepeer-review

42 Scopus citations


A polyelectrolyte complex(PEC) micelle-based siRNA delivery system has been developed for vascular endothelial growth factor (VEGF), and its antitumor efficacy has been demonstrated using in-vivo animal models. Penetration and distribution through the avascular regions of human solid tumors after extravasation are important issues for antitumor efficacy, especially for macromolecules such as VEGF siRNA PEC micelles. Using an in-vitro solid tumor model, multicellular layers(MCL) culture of human colorectal cancer cells, we evaluated the penetration kinetics and efficacy of VEGF siRNA PEC micelles(PEC-siRNA) in comparison to unmodified siRNA(N-siRNA). The PEC-siRNA showed full penetration (15-17 layers of cells) with a unique punctuated distribution pattern at 48 h following initial accumulation in the top layers and a significant suppression of mRNA and protein expression in a dose-dependent manner after 72 h exposure. Although the initial penetration of N-siRNA was faster than that of PEC-siRNA, N-siRNA showed complete loss of activity due to its instability within 24 h. Our data support the idea that PEC micelle formulation may provide stable penetration tool through the multilayers of cancer cells and ensure the gene silencing effect of VEGF. This study also demonstrated that MCL could serve as a useful in-vitro model to evaluate the dose- and time-dependent profiles of penetration and efficacy of macromolecular delivery systems in human solid tumor avascular regions.

Original languageEnglish
Pages (from-to)130-135
Number of pages6
JournalJournal of Controlled Release
Issue number2
StatePublished - 20 Jul 2009

Bibliographical note

Funding Information:
This work was supported by the Ministry of Education, Science and Technology (KBRDG of Next-Generation Growth Engine Project, F104AA010001-08A0101-00111; Nano Bio Regenomics Project, 2008-03767) and by the Ministry of Knowledge Economy (MKE) and the Korea Industrial Technology Foundation (KOTEF) through the Human Resource Training Project for Strategic Technology. A. M. Al-Abd was supported in part by a fellowship from the Korean Government Scholarship Program. We would like to express our sincere thanks to Joo-Ho Lee, M.S. for his kind assistance in preparing this manuscript.


  • Multicellular layers
  • Polyelectrolyte complex micelle
  • Solid tumors
  • Vascular endothelial growth factor
  • siRNA


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