Glutathione-depleting polyprodrug nanoparticle for enhanced photodynamic therapy and cascaded locoregional chemotherapy

J Colloid Interface Sci. 2024 Sep 15:670:279-287. doi: 10.1016/j.jcis.2024.05.086. Epub 2024 May 15.

Abstract

Nanomedicines that combine reactive oxygen species (ROS)-responsive polyprodrug and photodynamic therapy have shown great potential for improving treatment efficacy. However, the consumption of ROS by overexpressed glutathione in tumor cells is a major obstacle for achieving effective ROS amplification and prodrug activation. Herein, we report a polyprodrug-based nanoparticle that can realize ROS amplification and cascaded drug release. The nanoparticle can respond to the high level of hydrogen peroxide in tumor microenvironment, achieving self-destruction and release of quinone methide. The quinone methide depletes intracellular glutathione and thus decreases the antioxidant capacity of cancer cells. Under laser irradiation, a large amount of ROS will be generated to induce cell damage and prodrug activation. Therefore, the glutathione-depleting polyprodrug nanoparticles can efficiently inhibit tumor growth by enhanced photodynamic therapy and cascaded locoregional chemotherapy.

Keywords: Cancer therapy; Nanomedicine; Polyprodrug; Reactive oxygen species; Triggered drug release.

MeSH terms

  • Animals
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Drug Liberation
  • Drug Screening Assays, Antitumor
  • Glutathione* / chemistry
  • Glutathione* / metabolism
  • Humans
  • Hydrogen Peroxide / metabolism
  • Indolequinones
  • Mice
  • Nanoparticles* / chemistry
  • Particle Size
  • Photochemotherapy*
  • Photosensitizing Agents / administration & dosage
  • Photosensitizing Agents / chemistry
  • Photosensitizing Agents / pharmacology
  • Prodrugs* / chemistry
  • Prodrugs* / pharmacology
  • Reactive Oxygen Species* / metabolism
  • Surface Properties
  • Tumor Microenvironment / drug effects

Substances

  • Glutathione
  • Prodrugs
  • Reactive Oxygen Species
  • Antineoplastic Agents
  • Photosensitizing Agents
  • Hydrogen Peroxide
  • quinone methide
  • Indolequinones