Red/NIR-emissive AIE nanoprobe to track subcellular dynamics in a photodynamic therapy process

Yu Zhou1, Yalei Jiang1, Lanqiong Zhang2

  • 1School of Chemistry, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, Xi'an Jiaotong University, Xi'an, 710049, P. R. China. xuyanzi@xjtu.edu.cn.

Chemical Communications (Cambridge, England)
|December 5, 2025
PubMed

Insights

This study introduces a novel lysosome-specific nanoprobe for advanced cancer treatment monitoring. The probe allows high-resolution imaging of cellular processes and guides therapy by visualizing reactive oxygen species.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Cancer Research

Background:

  • Monitoring cancer treatment at the subcellular level is challenging.
  • Lysosomes play a crucial role in cellular processes and drug response.
  • Need for advanced imaging techniques for real-time treatment assessment.

Purpose of the Study:

  • To develop a lysosome-specific AIE nanoprobe for cancer treatment monitoring.
  • To integrate stimulated emission depletion (STED) imaging with photodynamic therapy.
  • To enable real-time visualization of lysosomal dynamics and apoptosis.

Main Methods:

  • Design and synthesis of a lysosome-specific Aggregation-Induced Emission (AIE) nanoprobe.
  • Utilizing Stimulated Emission Depletion (STED) microscopy for high-resolution imaging.
  • Employing photodynamic therapy to induce and monitor reactive oxygen species (ROS).

Main Results:

  • The nanoprobe specifically targets lysosomes.
  • Achieved real-time visualization of lysosomal dynamics.
  • Demonstrated ROS-mediated apoptosis visualization for treatment guidance.
  • High-resolution imaging capabilities were confirmed.

Conclusions:

  • The developed nanoprobe is a powerful tool for subcellular cancer treatment monitoring.
  • Offers a platform for high-resolution imaging-guided cancer diagnosis and therapy.
  • Facilitates real-time assessment of treatment efficacy through ROS detection.