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pH-responsive mesoporous Fe2O3–Au nanomedicine delivery system with magnetic targeting for cancer therapy

  • Beihang University

Research output: Contribution to journalArticlepeer-review

Abstract

Chemotherapy is the prime tool for the clinical treatment of cancer. The efficiency of treatment has been greatly improved with the assistance of nanomedicine delivery systems. However, it still meets the challenge of inefficient drug delivery and damage to normal tissues caused by uncontrolled drug release. Considering the various processes of nanomedicine acting on cancer cells, a pH-responsive mesoporous Fe2O3–Au nanomedicine delivery system with magnetic targeting was designed to achieve controlled drug release and improve the safety and efficiency. Fe2O3 particles were constructed with external mesopores and internal hollow structures, while Au nanoparticles were connected on the surface of Fe2O3 particles through pH-responsive valence bonds to encapsulate the drug. The Fe2O3–Au nanomedicine delivery system was equipped with magnetic targeting function, which could be induced by an external magnetic field to increase the drug concentration to kill cancer cells as well as reduce damage to normal cells. Meanwhile, based on the pH-responsive feature, the drug embedded could only be released in the weakly acidic condition of the cancer environment, while the nanomedicine delivery system remained closed in normal tissues. The Fe2O3–Au nanomedicine delivery system possessed the functions of pH responsiveness and magnetic targeting, enhancing safety and efficiency and providing a promising method for cancer therapy.

Original languageEnglish
Article number100127
JournalMedicine in Novel Technology and Devices
Volume15
DOIs
StatePublished - Sep 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Au nanoparticle
  • Cancer therapy
  • FeO
  • Magnetic nanomedicine delivery system
  • pH-responsive

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