Hierarchical targeted hepatocyte mitochondrial multifunctional chitosan nanoparticles for anticancer drug delivery

Biomaterials. 2015 Jun:52:240-50. doi: 10.1016/j.biomaterials.2015.02.001. Epub 2015 Feb 27.

Abstract

The overwhelming majority of drugs exert their pharmacological effects after reaching their target sites of action, however, these target sites are mainly located in the cytosol or intracellular organelles. Consequently, delivering drugs to the specific organelle is the key to achieve maximum therapeutic effects and minimum side-effects. In the work reported here, we designed, synthesized, and evaluated a novel mitochondrial-targeted multifunctional nanoparticles (MNPs) based on chitosan derivatives according to the physiological environment of the tumor and the requirement of mitochondrial targeting drug delivery. The intelligent chitosan nanoparticles possess various functions such as stealth, hepatocyte targeting, multistage pH-response, lysosomal escape and mitochondrial targeting, which lead to targeted drug release after the progressively shedding of functional groups, thus realize the efficient intracellular delivery and mitochondrial localization, inhibit the growth of tumor, elevate the antitumor efficacy, and reduce the toxicity of anticancer drugs. It provides a safe and efficient nanocarrier platform for mitochondria targeting anticancer drug delivery.

Keywords: Cancer therapy; Drug delivery; Hierarchical; Mitochondrial-targeted; Multifunctional nanoparticles; pH-response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Apoptosis
  • Chitosan / chemistry*
  • Chromatography, High Pressure Liquid
  • Cytoplasm / metabolism
  • Cytosol / metabolism
  • Drug Carriers / chemistry
  • Drug Delivery Systems
  • Drug Liberation
  • Hep G2 Cells
  • Hepatocytes / cytology*
  • Humans
  • Hydrogen-Ion Concentration
  • Lysosomes / metabolism
  • Male
  • Mice
  • Mice, Inbred ICR
  • Microscopy, Confocal
  • Mitochondria / metabolism*
  • Nanoparticles / chemistry*
  • Nanotechnology
  • Neoplasm Transplantation
  • Neoplasms / drug therapy
  • Rats
  • Rats, Wistar
  • Schiff Bases
  • Strychnine / analogs & derivatives
  • Strychnine / chemistry

Substances

  • Antineoplastic Agents
  • Drug Carriers
  • Schiff Bases
  • brucine
  • Chitosan
  • Strychnine