Reduction sensitive CC9-PEG-SSBPEI/miR-148b nanoparticles: Synthesis, characterization, targeting delivery and application for anti-metastasis

Colloids Surf B Biointerfaces. 2019 Nov 1:183:110412. doi: 10.1016/j.colsurfb.2019.110412. Epub 2019 Jul 31.

Abstract

miRNAs such as miR-148b play crucial regulatory role in tumor metastasis, but their applications are limited because they are easy to degrade in serum conditions and lack targeting ability. Herein, CC9-PEG-SSBPEI was synthesized and used as nano-carrier for miR-148b. DLS and gel retardation analyses indicated that CC9-PEG-SSBPEI could combine with miR-148b by charge interaction and formed into nanoparticles with the size changed from 811.6 nm to 146.4 nm. CC9-PEG-SSBPEI could protect miR-148b from RNase A degradation and showed a reduction sensitive release of miR-148b. FACS analysis and CLSM images displayed that the conjugated CC9 peptide improved the accumulation and penetration of the nanoparticles in HuH-7 liver cancer cells through binding with the target of miR-148b neuropilin-1(NRP-1) on the cell surface. The raised level of miR-148b in turn inhibited the expression of NRP-1 and suppressed the migration of HuH-7 liver cancer cells. Moreover, hemolysis and cytotoxicity assay demonstrated that the nanoparticles had good hemo- and cyto- compatibility. Hence, CC9-PEG-SSBPEI/miR-148b nanoparticles had the potential for targeting delivery of miR-148b and anti-metastasis of hepatocellular carcinoma (HCC) cells.

Keywords: CC9 peptide; Nanoparticles; Reduction sensitive; Targeting delivery; miR-148b.

MeSH terms

  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Erythrocytes / cytology
  • Gene Expression Regulation, Neoplastic*
  • Gene Targeting / methods*
  • Gene Transfer Techniques*
  • Hemolysis
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Humans
  • MicroRNAs / administration & dosage
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Nanoparticles / administration & dosage
  • Nanoparticles / chemistry*
  • Nanoparticles / metabolism
  • Neuropilin-1 / antagonists & inhibitors
  • Neuropilin-1 / genetics*
  • Neuropilin-1 / metabolism
  • Oligopeptides / chemistry
  • Oligopeptides / metabolism
  • Oxidation-Reduction
  • Particle Size
  • Polyethylene Glycols / chemistry
  • Polyethylene Glycols / metabolism
  • Polyethyleneimine / chemistry
  • Polyethyleneimine / metabolism
  • Ribonuclease, Pancreatic / chemistry

Substances

  • MIRN148 microRNA, human
  • MicroRNAs
  • NRP1 protein, human
  • Oligopeptides
  • Neuropilin-1
  • Polyethylene Glycols
  • Polyethyleneimine
  • Ribonuclease, Pancreatic