Oxygen depletion in FLASH ultra-high-dose-rate radiotherapy: A molecular dynamics simulation

TL;DR

This study uses molecular dynamics simulations to investigate how ultra-high-dose-rate radiotherapy reduces tissue damage by promoting the formation of less reactive oxygen species, explaining the FLASH effect.

Contribution

It introduces a first-principles simulation approach to elucidate oxygen depletion mechanisms and ROS dynamics in UHDR FLASH radiotherapy, providing molecular-level insights.

Findings

Formation of metastable ROS complexes at UHDR

NROS chains reduce bio-molecular damage

Higher dose rates increase NROS, decreasing toxic ROS

Abstract

We present a first-principles molecular dynamics (MD) simulation and expound upon a mechanism of oxygen depletion hypothesis to explain the mitigation of normal tissue injury observed in ultra-high-dose-rate (UHDR) FLASH radiotherapy. We simulated damage to a segment of DNA (also representing other bio-molecules such as RNA and proteins) in a simulation box filled with H$_2$O and O$_2$ molecules. Attoseconds physical interactions (ionizations, electronic and vibrational excitations) were simulated by using the Monte Carlo track structure code Geant4-DNA. Immediately after ionization, {\it ab initio} Car-Parrinello molecular dynamics (CPMD) simulation was used to identify which H$_2$O and O$_2$ molecules surrounding the DNA-molecule were converted into reactive oxygen species (ROS). Subsequently, the femto- to nano-second reactions of ROS were simulated by using MD with Reactive Force Field (ReaxFF), to illustrate ROS merging into new types of non-reactive oxygen species (NROS) due to strong coupling among ROS. Time-dependent molecular simulations revealed the formation of metastable and transient spaghetti-like complexes among ROS generated at UHDR. At the higher ROS densities produced under UHDR, stranded chains (i.e., NROS) are produced, mediated through attractive electric polarity forces, hydrogen bonds, and magnetic dipole-dipole interactions among hydroxyl (\ce{^{.}OH}) radicals. NROS tend to be less mobile than cellular biomolecules as opposed to the isolated and sparsely dense ROS generated at conventional dose rates (CDR). We attribute this effect to the suppression of bio-molecular damage induced per particle track. At a given oxygen level, as the dose rate increases, the size and number of NROS chains increase, and correspondingly the population of toxic ROS components decreases.