Binary and ternary complexes based on polycaprolactone-graft-poly (N, N-dimethylaminoethyl methacrylate) for targeted siRNA delivery

Yuanyu Huang, Daoshu Lin, Qian Jiang, Wendi Zhang, Shutao Guo, Ping Xiao, Shuquan Zheng, Xiaoxia Wang, Hongbo Chen, Hong Yan Zhang, Liandong Deng, Jinfeng Xing, Quan Du, Anjie Dong, Zicai Liang*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

50 Citations (Scopus)

Abstract

Small interfering RNA (siRNA) is a powerful gene silencing tool and has promising prospects in basic research and the development of therapeutic reagents However, the lack of an effective and safe tool for siRNA delivery hampers its application Here, we introduced binary and ternary complexes that effectively mediated siRNA-targeted gene silencing Both complexes showed excellent siRNA loading even at the low N/P/C ratio of 3:1:0 FACS and confocal microscopy demonstrated that nearly all cells robustly internalized siRNAs into the cytoplasm, where RNA interference (RNAi) occurred Luciferase assay and Western blot verified that silencing efficacy reached >80%, and introducing folate onto the ternary complexes further enhanced silencing efficacy by about 10% over those without folate at the same N/P/C ratio In addition, the coating of PGA- g-mPEG decreased the zeta potential almost to electroneutrality, and the MTT assay showed decreased cytotoxicity In vivo distribution measurement and histochemical analysis executed in C57BL/6 and Hela tumor-bearing BALB/c nude mice showed that complexes accumulated in the liver, lungs, pancreas and tumors and were released slowly for a long time after intravenous injection Furthermore, ternary complexes showed higher siRNA fluorescence intensity than binary complexes at the same N/P ratio in tumor tissues, those with folate delivered more siRNAs to tumors than those without folate, and more folate induced more siRNA transport to tumors In addition, in vivo functional study showed that both binary and ternary complexes mediated down-regulation of ApoB in liver efficiently and consequently blocked the secretion of fatty acids into the blood, resulted in lipid accumulation in liver, liver steatosis and hepatic dysfunction In conclusion, these complexes provided a powerful means of administration for siRNA-mediated treatment of liver-related diseases and various cancers, especial for pancreatic and cervical cancer.

Original languageEnglish
Pages (from-to)4653-4664
Number of pages12
JournalBiomaterials
Volume33
Issue number18
DOIs
Publication statusPublished - Jun 2012
Externally publishedYes

Keywords

  • Liver targeting
  • Non-viral carriers
  • PCL-g-PDMAEMA
  • SiRNA delivery
  • Ternary complex
  • Tumor targeting

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