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.