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Tuning the pH-Switch of Supramolecular Polymer Carriers for siRNA to Physiologically Relevant pH.

Patrick AhlersHendrik FrischRegina HolmDaniel SpitzerMatthias BarzPol Besenius
Published in: Macromolecular bioscience (2017)
The preparation of histidine enriched dendritic peptide amphiphiles and their self-assembly into multicomponent pH-switchable supramolecular polymers is reported. Alternating histidine and phenylalanine peptide synthons allow the assembly/disassembly to be adjusted in a physiologically relevant range of pH 5.3-6.0. Coassembly of monomers equipped with dendritic tetraethylene glycol chains with monomers bearing peripheral primary amine groups leads to nanorods with a tunable cationic surface charge density. These surface functional supramolecular polycations are able to reversibly bind short interfering RNA (siRNA). The nanorod-like supramolecular polymers, their complexation with siRNA, and the pH-triggered assembly/disassembly of the supramolecular carriers are characterized via circular dichroism spectroscopy, gel electrophoresis, as well as transmission electron microscopy. Multicomponent supramolecular polymers represent a modular and promising strategy for applications as responsive carrier vehicles, codelivery strategies, and gene therapy.
Keyphrases
  • energy transfer
  • water soluble
  • cancer therapy
  • gene therapy
  • hyaluronic acid
  • drug delivery
  • single molecule
  • simultaneous determination
  • tandem mass spectrometry