Systematic Development and Optimization of Inhalable Pirfenidone Liposomes for Non-Small Cell Lung Cancer Treatment

Vineela Parvathaneni1, Nishant S Kulkarni1, Snehal K Shukla1

  • 1Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA.

Pharmaceutics
|March 4, 2020
PubMed

Insights

Repurposing pirfenidone (PFD) in liposomes offers a promising new treatment for non-small cell lung cancer (NSCLC). This drug delivery method enhanced anti-cancer effects in laboratory and ex-vivo models.

Area of Science:

  • Oncology
  • Drug Delivery
  • Nanotechnology

Background:

  • Non-small cell lung cancer (NSCLC) presents limited treatment options due to drug resistance and off-target effects.
  • Drug discovery is costly and time-consuming; drug repurposing offers a faster alternative.
  • Pirfenidone (PFD), an anti-fibrotic drug, is explored for novel therapeutic applications.

Purpose of the Study:

  • To repurpose pirfenidone (PFD) for non-small cell lung cancer (NSCLC) treatment.
  • To develop and evaluate PFD-loaded cationic liposomes for enhanced NSCLC therapy.
  • To assess the in-vitro and ex-vivo efficacy and mechanism of action of liposomal PFD.

Main Methods:

  • Optimized liposomal formulations of PFD for physicochemical properties and aerosol deposition.
  • Evaluated cellular uptake, anti-cancer activity (colony formation, migration, apoptosis, angiogenesis) in NSCLC cell lines.
  • Assessed therapeutic potential using 3D tumor spheroid models (ex-vivo).

Main Results:

  • PFD-loaded liposomes demonstrated significant reduction in NSCLC cell growth (1.5- to 2-fold).
  • Liposomal PFD exhibited enhanced anti-cancer effects on migration, apoptosis, and angiogenesis.
  • Ex-vivo studies showed superior efficacy of liposomal PFD compared to free PFD in tumor spheroids.

Conclusions:

  • Inhalable liposome-encapsulated pirfenidone shows significant potential for NSCLC treatment.
  • The developed formulation enhances PFD's anti-cancer activity through improved delivery.
  • Further in vivo preclinical and clinical studies are warranted to validate efficacy.