Inorganic nanoparticle agents for enhanced chemodynamic therapy of tumours

Sagang Koo1,2, Young Geon Kim1,2, Nohyun Lee3

  • 1Center for Nanoparticle Research, Institute for Basic Science (IBS), Seoul 08826, Republic of Korea.

Nanoscale
|August 14, 2023
PubMed

Insights

Chemodynamic therapy (CDT) uses inorganic nanoparticles to selectively kill cancer cells by increasing oxidative stress. This review explores strategies to enhance CDT efficacy and discusses challenges for clinical application.

Area of Science:

  • Biomedical Engineering
  • Nanomedicine
  • Oncology

Background:

  • Oxidative species play a role in diseases, prompting interest in redox-active inorganic nanomaterials for nanomedicine.
  • While reducing oxidative stress has shown success, increasing it to kill malignant cells using nanomaterials has been inefficient.
  • Chemodynamic therapy (CDT) offers a selective approach by leveraging the tumor microenvironment.

Purpose of the Study:

  • To review strategies for improving chemodynamic therapy (CDT) performance using inorganic nanoparticles.
  • To explore underlying mechanisms and factors influencing CDT efficacy.
  • To discuss challenges and future directions for clinical translation.

Main Methods:

  • Literature review of recent strategies and mechanisms in inorganic nanoparticle-based CDT.
  • Analysis of the tumor microenvironment's role (acidity, hydrogen peroxide, antioxidants).
  • Discussion of modulating these factors and combination therapy approaches.

Main Results:

  • Various strategies have been developed to enhance CDT performance using inorganic nanoparticles.
  • Tumor microenvironment factors significantly impact CDT efficacy and selectivity.
  • Modulation of the tumor microenvironment and combination therapies show promise.

Conclusions:

  • Inorganic nanoparticles offer promising strategies for enhancing chemodynamic therapy.
  • Optimizing CDT requires understanding and manipulating the tumor microenvironment.
  • Further research is needed to address challenges for clinical translation of CDT.