Functionalized large pore mesoporous silica nanoparticles for gene delivery featuring controlled release and co-delivery

  • Sandy Budi Hartono
  • , Nghia Truong Phuoc
  • , Meihua Yu
  • , Zhongfan Jia
  • , Michael J. Monteiro*
  • , Shizhang Qiao
  • , Chengzhong Yu
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

109 Scopus citations

Abstract

Novel mesoporous silica nanoparticles (LPMSNs) functionalised with degradable poly(2-dimethylaminoethyl acrylate) (PDMAEA) have been developed (PDMAEA-LPMSNs) as nano-carriers for gene delivery. The unique design of PDMAEA-LPMSNs has endowed this system with multiple functions derived from both the organic and inorganic moieties. The cationic polymer unit binds to genetic molecules and undergoes a self-catalyzed hydrolysis in water to form a non-toxic anionic polymer poly(acrylic acid), allowing controlled release of siRNA in the cells. The nanopores of the LPMSNs provide a reservoir for storage and release of chloroquine to facilitate endosomal escape. The PDMAEA-LPMSN composites were characterized by elemental analysis (EA), X-ray photoelectron spectroscopy (XPS), solid-state 13C magic-angle spinning nuclear magnetic resonance (MAS-NMR), thermogravimetric analysis (TGA), and nitrogen sorption techniques. Their siRNA delivery performance was tested in a KHOS cell line, showing promising potential for co-delivery of genes and drugs.

Original languageEnglish
Pages (from-to)718-726
Number of pages9
JournalJournal of Materials Chemistry B
Volume2
Issue number6
DOIs
StatePublished - 14 Feb 2014
Externally publishedYes

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