EphA2 targeting pegylated nanocarrier drug delivery system for treatment of lung cancer

Pharm Res. 2014 Oct;31(10):2796-809. doi: 10.1007/s11095-014-1377-4. Epub 2014 May 29.

Abstract

Purpose: Evaluation of tumor targeting pegylated EphA2 peptide coated nanoparticles (ENDDs) of a novel anticancer agent DIM-C-pPhC6H5 (DIM-P) and Docetaxel (DOC) and investigate its antitumor activity and potential for treatment of lung cancer.

Methods: Nanoparticles were prepared with DIM-P and DOC (NDDs) using Nano-DeBEE. ENDDs were prepared by conjugating NDDs with 6His-PEG2K-EphA2 peptide and characterized for physicochemical properties, binding assay, cytotoxicity, cellular uptake studies, drug release and pharmacokinetic parameters. Anti-tumor activity of ENDDs was evaluated using a metastatic H1650 and orthotopic A549 tumor models in nude mice and tumor tissue were analyzed by RT-PCR and immunohistochemistry.

Results: Particle size and entrapment efficiency of ENDDs were 197 ± 21 nm and 95 ± 2%. ENDDs showed 32.5 ± 3.5% more cellular uptake than NDDs in tumor cells. ENDDs showed 23 ± 3% and 26 ± 4% more tumor reduction compared to NDDs in metastatic and orthotopic tumor models, respectively. In-vivo imaging studies using the Care stream MX FX Pro system showed (p < 0.001) 40-60 fold higher flux for ENDDs compared to NDDs at tumor site.

Conclusions: The results emanating from these studies demonstrate anti-cancer potential of DIM-P and the role of ENDDs as effective tumor targeting drug delivery systems for lung cancer treatment.

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / therapeutic use
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Drug Carriers / chemistry*
  • Endocytosis
  • Humans
  • Indoles / administration & dosage
  • Indoles / pharmacokinetics
  • Indoles / therapeutic use
  • Ligands
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology
  • Mice, Inbred BALB C
  • Mice, Nude
  • Molecular Targeted Therapy
  • Nanoparticles / chemistry*
  • PPAR gamma / agonists
  • Polyethylene Glycols / chemistry*
  • Protein Binding
  • Receptor, EphA2 / metabolism*
  • Xenograft Model Antitumor Assays

Substances

  • 1,1-bis(3'-indolyl)-1-(4-biphenyl)methane
  • Antineoplastic Agents
  • Drug Carriers
  • Indoles
  • Ligands
  • PPAR gamma
  • Polyethylene Glycols
  • Receptor, EphA2