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Terbium-Rose Bengal Coordination Nanocrystals-Induced ROS Production under Low-Dose X-rays in Cultured Cancer Cells
Debabrata Maiti1, Hao Yu2, Yuki Mochida3
1Department of Materials Engineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
ACS Applied Bio Materials
|June 8, 2023
Summary
Terbium (Tb)-rose bengal (RB) coordination nanocrystals (T-RBNs) enhance X-ray-induced photodynamic therapy (X-PDT) by increasing reactive oxygen species (ROS) production. These T-RBNs effectively destroy cancer cells with low X-ray doses, offering a promising new cancer treatment.
Area of Science:
- Nanotechnology
- Biomedical Engineering
- Radiotherapy
Background:
- X-ray-induced photodynamic therapy (X-PDT) offers targeted cancer treatment.
- Developing efficient scintillators (Sc) and photosensitizers (Ps) is crucial for low-dose X-PDT.
- Reducing energy loss between components enhances reactive oxygen species (ROS) generation.
Purpose of the Study:
- To design and synthesize novel terbium (Tb)-rose bengal (RB) coordination nanocrystals (T-RBNs).
- To investigate the efficiency of T-RBNs in generating ROS under X-ray irradiation.
- To evaluate the therapeutic potential of T-RBNs for X-PDT in cancer treatment.
Main Methods:
- Solvothermal synthesis of T-RBNs with a specific [RB]/[Tb] molar ratio.
- Characterization of T-RBNs size, crystallinity, and chemical coordination using techniques like Fourier transform infrared spectroscopy.
- Assessment of ROS production (singlet oxygen and hydroxyl radicals) under low-dose X-ray irradiation (0.5 Gy).
- In vitro cytotoxicity and cellular uptake studies using 4T1-luc cancer cells.
- Evaluation of DNA damage via phosphorylated γ-H2AX staining and cell death pathways (apoptosis/necrosis).
Main Results:
- T-RBNs were successfully synthesized with controlled size (6.8 ± 1.2 nm) and crystalline properties.
- T-RBNs demonstrated significantly enhanced ROS production (∼8-fold higher than bare RB).
- T-RBNs showed low cytotoxicity and efficient internalization into 4T1-luc cells.
- X-ray irradiation of T-RBNs induced significant DNA double-strand damage and >70% cancer cell death.
- T-RBNs exhibited superior ROS generation compared to inorganic nanoparticle controls.
Conclusions:
- T-RBNs serve as an effective Sc/Ps platform for X-PDT.
- The developed T-RBNs enhance ROS production efficiency, crucial for low-dose X-PDT.
- T-RBNs show significant potential for advanced cancer therapy by inducing targeted cancer cell death.

