A novel method for conjugating the terminal amine of peptide ligands to cholesterol: synthesis iRGD-cholesterol

Ther Deliv. 2019 Jan;10(1):11-20. doi: 10.4155/tde-2018-0057.

Abstract

Aim: Conventional conjugation reactions often involve the use of activated PEG as a linker, but concerns about PEG-mediated reduction in intracellular delivery and enhanced immunogenicity have generated interest in developing methods that eliminate the need for a PEG linker.

Materials & methods: Reaction conditions were identified that specifically couples the terminal amine of a cyclic iRGD peptide (CRGDRGPDC) to the hydroxyl moiety of cholesterol through a short carbamate linker.

Results & conclusion: Using this method for synthesizing iRGD-cholesterol, peptide ligands can be incorporated into lipid-based delivery systems, thereby eliminating concerns about adverse reactions to PEG. Toxicity and stability data indicate low toxicity and adequate serum stability at low ligand levels.

Keywords: nanotechnology; oligonucleotides; targeting – cellular.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Chemistry Techniques, Synthetic / methods*
  • Cholesterol / chemistry*
  • Cholesterol / toxicity
  • Drug Carriers / chemical synthesis*
  • Drug Carriers / toxicity
  • Ligands
  • Mice
  • Oligopeptides / chemistry*
  • Oligopeptides / toxicity
  • Particle Size
  • Polyethylene Glycols / adverse effects
  • Polyethylene Glycols / chemistry
  • Toxicity Tests

Substances

  • Drug Carriers
  • Ligands
  • N-end cysteine peptide tumor-homing peptide
  • Oligopeptides
  • Polyethylene Glycols
  • Cholesterol