Functionalization of carboxylated lignin nanoparticles for targeted and pH-responsive delivery of anticancer drugs

Nanomedicine (Lond). 2017 Nov;12(21):2581-2596. doi: 10.2217/nnm-2017-0219. Epub 2017 Sep 29.

Abstract

Aim: To carboxylate kraft lignin toward the functionalization of carboxylated lignin nanoparticles (CLNPs) with a block copolymer made of PEG, poly(histidine) and a cell-penetrating peptide and then evaluate the chemotherapeutic potential of the innovative nanoparticles.

Materials & methods: The produced nanoparticles were characterized and evaluated in vitro for stability and biocompatibility and the drug release profiles and antiproliferative effect were also assessed.

Results: The prepared CLNPs showed spherical shape and good size distribution, good stability in physiological media and low cytotoxicity in all the tested cell lines. A poorly water-soluble cytotoxic agent was successfully loaded into the CLNPs, improving its release profiles in a pH-sensitive manner and showing an enhanced antiproliferative effect in the different cancer cells compared with a normal endothelial cell line.

Conclusion: The resulting CLNPs are promising candidates for anticancer therapy.

Keywords: antiproliferative effect; benzazulene; carboxylated lignin nanoparticles; drug loading; pH-responsive release; targeting functionalization.

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cell-Penetrating Peptides / chemistry
  • Drug Carriers / chemistry*
  • Drug Liberation
  • Histidine / chemistry
  • Humans
  • Hydrogen-Ion Concentration
  • Lignin / chemistry*
  • Materials Testing
  • Nanoparticles / chemistry*
  • Particle Size
  • Polyethylene Glycols / chemistry
  • Surface Properties

Substances

  • Antineoplastic Agents
  • Cell-Penetrating Peptides
  • Drug Carriers
  • polyhistidine
  • Polyethylene Glycols
  • Histidine
  • Lignin