Self-assembly of amphiphilic tripeptides into nanoparticles for drug delivery

Protein Pept Lett. 2014;21(2):194-9. doi: 10.2174/09298665113206660117.

Abstract

Peptide-based nanomaterials are widely used as nanocarriers for catalysis, drug delivery, and gene delivery. In this paper, we designed and synthesized the amphiphilic tripeptides through solution phase synthesis. The tripeptides were purified by column chromatography and the molecular structures were confirmed by (1)H NMR and TOF-MS. The tripeptides could self-assemble into spherical nanoparticles in aqueous media with a low critical aggregation concentration. The size and morphology of the nanoparticles were performed by dynamic light scattering, scanning electron microscopy and transmission electron microscope. The peptide-based nanoparticles were used as biocompatible nanocarriers for encapsulating hydrophobic doxorubicin (DOX) to achieve controlled release. The CCK-8 assay indicated that the peptide-based nanocarriers could enhance cellular uptake and drug efficacy of DOX to A549 tumor cell line. These results showed that the self-assembly of amphiphilic tripeptides provided a facile strategy to fabricate nanoparticles for anti-tumor drug delivery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / metabolism
  • Biological Transport
  • Cell Line, Tumor
  • Doxorubicin / chemistry
  • Doxorubicin / metabolism
  • Drug Carriers / chemistry*
  • Humans
  • Hydrophobic and Hydrophilic Interactions*
  • Lysine / chemistry
  • Models, Molecular
  • Molecular Conformation
  • Molecular Weight
  • Nanoparticles / chemistry*
  • Oligopeptides / chemistry*
  • Phenylalanine / chemistry

Substances

  • Antineoplastic Agents
  • Drug Carriers
  • Oligopeptides
  • Phenylalanine
  • Doxorubicin
  • Lysine