Supramolecular pseudo-block gene carriers based on bioreducible star polycations

Biomaterials. 2013 Jul;34(21):5411-22. doi: 10.1016/j.biomaterials.2013.03.092. Epub 2013 Apr 20.

Abstract

A series of supramolecular pseudo-block polycations (CD-SS-pDM/Ad-pPEGs) were realized by assembling bioreducible β-cyclodextrin-cored star poly (2-dimethyl amino)ethyl methacrylate with different molecular weight and an adamantine-ended linear poly(poly(ethylene glycol)ethyl ether methacrylate) (pPEGEEMA) via the host-guest interaction. The pseudo-block CD-SS-pDM/Ad-pPEG carriers were investigated in terms of DNA binding capability, cytotoxicity, gene transfection in HepG2 and COS7 cell lines, and in vivo anti-tumor activity. The pseudo-block carriers exhibited undiminished pDNA-condensing abilities compared with the starting star carriers. Meanwhile, the pseudo-block carriers displayed lower cytotoxicity and higher gene transfection efficiencies at various N/P ratios. These results are consistent with the favorable properties of pPEGEEMA as expected. Furthermore, cellular internalization results and in vivo anti-tumor activity analysis demonstrated that assembled pPEGEEMA could enhance the stability of pseudo-block carriers, thus improving their cellular internalization and gene transfection efficiency. The present study demonstrated that supramolecular pseudo-block polycations via the host-guest interaction is an effective means to produce new gene carriers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Biocompatible Materials / chemistry*
  • COS Cells
  • Cell Survival / drug effects
  • Chlorocebus aethiops
  • DNA / metabolism
  • Dimethyl Sulfoxide / chemistry
  • Endocytosis / drug effects
  • Ethylamines / chemical synthesis
  • Ethylamines / chemistry*
  • Gene Transfer Techniques*
  • Green Fluorescent Proteins / metabolism
  • Hep G2 Cells
  • Humans
  • Immunohistochemistry
  • Magnetic Resonance Spectroscopy
  • Methacrylates / chemical synthesis
  • Methacrylates / chemistry*
  • Mice
  • Microscopy, Atomic Force
  • Particle Size
  • Plasmids / metabolism
  • Polyamines / chemistry*
  • Polyelectrolytes
  • Polyethylene Glycols / chemical synthesis
  • Polyethylene Glycols / chemistry*
  • Static Electricity
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism
  • beta-Cyclodextrins / chemical synthesis
  • beta-Cyclodextrins / chemistry

Substances

  • 2-dimethylaminoethyl methacrylate
  • Antineoplastic Agents
  • Biocompatible Materials
  • Ethylamines
  • Methacrylates
  • Polyamines
  • Polyelectrolytes
  • Tumor Suppressor Protein p53
  • beta-Cyclodextrins
  • enhanced green fluorescent protein
  • polycations
  • polyethylene glycol methacrylate
  • Green Fluorescent Proteins
  • Polyethylene Glycols
  • DNA
  • Dimethyl Sulfoxide