Gold-Nanoparticles-Enhanced Production of Reactive Oxygen Species in Cells at Spread-Out Bragg Peak under Proton Beam Radiation

被引:11
作者
Lo, Chang-Yun [1 ]
Tsai, Shiao-Wen [2 ,3 ]
Niu, Huan [4 ]
Chen, Fang-Hsin [5 ,6 ,7 ,8 ]
Hwang, Hsiao-Chien [9 ]
Chao, Tsi-Chian [7 ]
Hsiao, Ing-Tsung [7 ]
Liaw, Jiunn-Woei [1 ,9 ,10 ]
机构
[1] Chang Gung Univ, Dept Mech Engn, Taoyuan 333, Taiwan
[2] Chang Gung Univ, Dept Biomed Engn, Taoyuan 333, Taiwan
[3] Chang Gung Mem Hosp, Dept Periodont, Taipei 105, Taiwan
[4] Natl Tsing Hua Univ, Nucl Sci & Technol Dev Ctr, Accelerator Lab, Hsinchu 300, Taiwan
[5] Natl Tsing Hua Univ, Inst Nucl Engn & Sci, Hsinchu 300, Taiwan
[6] Chang Gung Mem Hosp, Dept Radiat Oncol, Taoyuan 333, Taiwan
[7] Chang Gung Univ, Dept Med Imaging & Radiol Sci, Taoyuan 333, Taiwan
[8] Sci Natl Tsing Hua Univ, Inst Nucl Engn, Hsinchu, Taiwan
[9] Linkou Chang Gung Mem Hosp, Proton & Radiat Therapy Ctr, Taoyuan 333, Taiwan
[10] Ming Chi Univ Technol, Dept Mech Engn, New Taipei City 243, Taiwan
关键词
RELATIVE BIOLOGICAL EFFECTIVENESS; DOSE ENHANCEMENT; DNA-DAMAGE; THERAPY; RADIOSENSITIZATION; RADIOTHERAPY; CANCER; RBE; SIMULATION; ENERGY;
D O I
10.1021/acsomega.3c01025
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study investigates the radiobiological effects of gold nanoparticles (GNPs) as radiosensitizers for proton beam therapy (PBT). Specifically, we explore the enhanced production of reactive oxygen species (ROS) in GNP-loaded tumor cells irradiated by a 230 MeV proton beam in a spread-out Bragg peak (SOBP) zone obtained by a passive scattering system. Our findings indicate that the radiosensitization enhancement factor is 1.24 at 30% cell survival fraction, 8 days after 6 Gy proton beam irradiation. Since protons deposit the majority of their energy at the SOBP region and interact with GNPs to induce more ejected electrons from the high-Z GNPs, these ejected electrons then react with water molecules to produce excessive ROS that can damage cellular organelles. Laser scanning confocal microscopy reveals the excessive ROS induced inside the GNP-loaded cells immediately after proton irradiation. Furthermore, the damage to cytoskeletons and mitochondrial dysfunction in GNP-loaded cells caused by the induced ROS becomes significantly severe, 48 h after proton irradiation. Our biological evidence suggests that the cytotoxicity of GNP-enhanced ROS production has the potential to increase the tumoricidal efficacy of PBT.
引用
收藏
页码:17922 / 17931
页数:10
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