Terbium-Rose Bengal Coordination Nanocrystals-Induced ROS Production under Low-Dose X-rays in Cultured Cancer Cells for Photodynamic Therapy.
Debabrata MaitiHao YuYuki MochidaSeongyeon WonShinichi YamashitaMitsuru NaitoKanjiro MiyataHyun Jin KimPublished in: ACS applied bio materials (2023)
X-ray-triggered scintillators (Sc) and photosensitizers (Ps) have been developed for X-ray-induced photodynamic therapy (X-PDT) to selectively destruct deep tissue tumors with a low X-ray dose. This study designed terbium (Tb)-rose bengal (RB) coordination nanocrystals (T-RBNs) by a solvothermal treatment, aiming to reduce photon energy dissipation between Tb 3+ and RB and thus increase the reactive oxygen species (ROS) production efficiency. T-RBNs synthesized at a molar ratio of [RB]/[Tb] = 3 exhibited a size of 6.8 ± 1.2 nm with a crystalline property. Fourier transform infrared analyses of T-RBNs indicated successful coordination between RB and Tb 3+ . T-RBNs generated singlet oxygen ( 1 O 2 ) and hydroxyl radicals ( • OH) under low-dose X-ray irradiation (0.5 Gy) via scintillating and radiosensitizing pathways. T-RBNs produced ∼8-fold higher ROS amounts than bare RB and ∼3.6-fold higher ROS amounts than inorganic nanoparticle-based controls. T-RBNs did not exhibit severe cytotoxicity up to 2 mg/mL concentration in cultured luciferase-expressing murine epithelial breast cancer (4T1-luc) cells. Furthermore, T-RBNs were efficiently internalized into cultured 4T1-luc cells and induced DNA double strand damage, as evidenced by an immunofluorescence staining assay with phosphorylated γ-H 2 AX. Ultimately, under 0.5 Gy X-ray irradiation, T-RBNs induced >70% 4T1-luc cell death via simultaneous apoptosis/necrosis pathways. Overall, T-RBNs provided a promising Sc/Ps platform under low-dose X-PDT for advanced cancer therapy.
Keyphrases
- photodynamic therapy
- cell death
- low dose
- cell cycle arrest
- reactive oxygen species
- high glucose
- high resolution
- diabetic rats
- oxidative stress
- mycobacterium tuberculosis
- dna damage
- endothelial cells
- high dose
- drug induced
- induced apoptosis
- fluorescence imaging
- cancer therapy
- drug delivery
- endoplasmic reticulum stress
- computed tomography
- pi k akt
- room temperature
- combination therapy