Boosting Hydroxyl Radical Generation with Nitrogen Vacancy-Modified Carbon Nitride for Triggering Dual Damage of Cancer Nucleus DNA-Mitochondria against Hypoxic Tumors

Int J Nanomedicine. 2025 Jul 5:20:8765-8781. doi: 10.2147/IJN.S515726. eCollection 2025.

Abstract

Introduction: Oral squamous cell carcinoma (OSCC) is a prevalent and deadly cancer, with over 350,000 new cases yearly. A hypoxic tumor microenvironment is the bottleneck of photodynamic therapy (PDT) and significantly weakens overall therapeutic efficacy.

Methods: In this study, we introduce nitrogen vacancy-modified PCN (NV-PCN), a novel metal-free and O2-independent photosensitizer designed for PDT. NV-PCN targets Cal-27-induced OSCC by reducing highly expressed H2O2 in tumors to highly reactive •OH. This innovative approach aims to overcome the limitations posed by the hypoxic environment and enhance the effectiveness of PDT in treating OSCC.

Results: The introduction of NV not only further improves the cell accessibility of PCN by increasing the content of -NH2 but also provides more reactive sites for H2O2 reduction and facilitates carrier separation. Under illumination, NV-PCN generates a burst of •OH around the nuclei and mitochondria of Cal-27 cells, which effectively kills the cells via synchronously leading to DNA damage and mitochondrial dysfunction. Compared to the conventional photosensitizer chlorin e6, NV-PCN-based PDT exhibits excellent anticancer performance in vitro and in vivo, highlighting its potential as a next-generation therapeutic agent.

Conclusion: Collectively, the high •OH-generation efficiency, strong anticancer activity, and overall safety of the O2-independent nanoparticle opens up new avenues for in-depth study on carbon nitride-based cancer PDT strategies. This work offers new hope for the effective treatment of OSCC and other challenging cancers.

Keywords: DNA-damage repair; hydroxyl radical; nitrogen vacancy; photodynamic therapy; polymeric carbon nitride.

MeSH terms

  • Animals
  • Carcinoma, Squamous Cell* / drug therapy
  • Carcinoma, Squamous Cell* / pathology
  • Cell Line, Tumor
  • Cell Nucleus / drug effects
  • Chlorophyllides
  • DNA Damage / drug effects
  • Humans
  • Hydrogen Peroxide / metabolism
  • Hydroxyl Radical* / chemistry
  • Hydroxyl Radical* / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mouth Neoplasms* / drug therapy
  • Mouth Neoplasms* / pathology
  • Nitriles* / chemistry
  • Nitriles* / pharmacology
  • Nitrogen / chemistry
  • Photochemotherapy / methods
  • Photosensitizing Agents* / chemistry
  • Photosensitizing Agents* / pharmacology
  • Porphyrins / pharmacology
  • Tumor Hypoxia / drug effects
  • Tumor Microenvironment / drug effects

Substances

  • Photosensitizing Agents
  • Nitrogen
  • Hydroxyl Radical
  • Nitriles
  • cyanogen
  • Hydrogen Peroxide
  • Chlorophyllides
  • Porphyrins