Receptor-Mediated Targeted Delivery of Surface-ModifiedNanomedicine in Breast Cancer: Recent Update and Challenges

Md Rizwanullah1, Mohammad Zaki Ahmad2, Mohammed M Ghoneim3

  • 1Department of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi 110062, India.

Pharmaceutics
|December 28, 2021
PubMed

Insights

Targeted nanomedicines offer improved breast cancer treatment by enhancing drug delivery. Exploiting specific receptors on cancer cells with novel nanoparticulate systems shows promise in preclinical models.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Oncology

Background:

  • Breast cancer treatment faces challenges due to poor drug targeting, tumor microenvironment, and multidrug resistance.
  • Conventional chemotherapy has limitations in efficacy and specificity for breast cancer.
  • Developing targeted drug delivery systems is crucial for overcoming these obstacles.

Purpose of the Study:

  • To review targeted delivery approaches for breast cancer using nanoparticulate systems.
  • To explore the use of multiple targeting ligands for receptor-mediated drug uptake.
  • To discuss the therapeutic efficacy of these novel approaches in preclinical models.

Main Methods:

  • Review of literature on surface-modified nanomedicines for breast cancer.
  • Analysis of nanoparticulate systems with multiple targeting ligands.
  • Evaluation of receptor-mediated cellular uptake mechanisms.

Main Results:

  • Surface-modified nanomedicines can enhance drug-loaded nanoparticulate construct delivery.
  • Targeting overexpressed receptors on breast cancer cells improves cellular uptake.
  • Preclinical studies demonstrate the therapeutic efficacy of these targeted approaches.

Conclusions:

  • Receptor-targeted nanomedicines show significant potential for breast cancer treatment.
  • Addressing the translational gap between laboratory research and clinical application is key.
  • Future directions should focus on refining nanomedicine development for clinical success.