Nanomedicine Strategies Utilizing Lipid-Based Nanoparticles for Liver Cancer Therapy: Exploring Signaling Pathways

Fereshteh Asgharzadeh1, Maryam Moradi Binabaj2, Sahar Fanoudi3

  • 1Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

PubMed

Insights

Lipid-based nanoparticles (LNPs) show promise for improving drug delivery in liver cancer (hepatocellular carcinoma, HCC) treatment. This review explores LNPs

Area of Science:

  • Oncology and Nanomedicine: Focus on hepatocellular carcinoma (HCC) and therapeutic drug delivery systems.

Background:

  • Hepatocellular carcinoma (HCC) is a leading cause of cancer mortality with limited survival rates.
  • Current HCC treatments face challenges due to impaired drug delivery in the diseased liver.
  • Lipid-based nanoparticles (LNPs) offer a potential solution for enhanced drug targeting and efficacy.

Purpose of the Study:

  • To review the current applications of lipid-based nanoparticles (LNPs) in developing anti-HCC therapies.
  • To highlight the potential of LNPs in overcoming drug delivery barriers in liver cancer.
  • To identify future directions and advancements in LNP-based HCC treatment.

Main Methods:

  • Comprehensive literature review of existing research on LNPs for HCC therapy.
  • Analysis of LNP structural properties and their impact on drug delivery.
  • Examination of diverse therapeutic cargos and their compatibility with LNPs.

Main Results:

  • LNPs demonstrate versatile structural configurations for improved physical stability.
  • LNPs can accommodate various therapeutic agents with different properties.
  • Existing research indicates significant potential for LNPs in anti-HCC drug development.

Conclusions:

  • Lipid-based nanoparticles represent a promising platform for advancing hepatocellular carcinoma treatment.
  • Further research into LNP applications could overcome critical drug delivery challenges in HCC.
  • LNPs offer a pathway to improved therapeutic outcomes for liver cancer patients.