Proton Irradiations at Ultra-High Dose Rate vs. Conventional Dose Rate: Strong Impact on Hydrogen Peroxide Yield.


Journal

Radiation research
ISSN: 1938-5404
Titre abrégé: Radiat Res
Pays: United States
ID NLM: 0401245

Informations de publication

Date de publication:
01 09 2022
Historique:
received: 11 01 2022
accepted: 25 05 2022
pubmed: 9 6 2022
medline: 11 9 2022
entrez: 8 6 2022
Statut: ppublish

Résumé

During ultra-high dose rate (UHDR) external radiation therapy, healthy tissues appear to be spared while tumor control remains the same compared to conventional dose rate. However, the understanding of radiochemical and biological mechanisms involved are still to be discussed. This study shows how the hydrogen peroxide (H2O2) production, one of the reactive oxygen species (ROS), could be controlled by early heterogenous radiolysis processes in water during UHDR proton-beam irradiations. Pure water was irradiated in the plateau region (track-segment) with 68 MeV protons under conventional (0.2 Gy/s) and several UHDR conditions (40 Gy/s to 60 kGy/s) at the ARRONAX cyclotron. Production of H2O2 was then monitored using the Ghormley triiodide method. New values of GTS(H2O2) were added in conventional dose rate. A substantial decrease in H2O2 production was observed from 0.2 to 1.5 kGy/s with a more dramatic decrease below 100 Gy/ s. At higher dose rate, up to 60 kGy/s, the H2O2 production stayed stable with a mean decrease of 38% ± 4%. This finding, associated to the decrease in the production of hydroxyl radical (•OH) already observed in other studies in similar conditions can be explained by the well-known spur theory in radiation chemistry. Thus, a two-step FLASH-RT mechanism can be envisioned: an early step at the microsecond scale mainly controlled by heterogenous radiolysis, and a second, slower, dominated by O2 depletion and biochemical processes. To validate this hypothesis, more measurements of radiolytic species will soon be performed, including radicals and associated lifetimes.

Identifiants

pubmed: 35675499
pii: 482778
doi: 10.1667/RADE-22-00021.1
doi:

Substances chimiques

Protons 0
Water 059QF0KO0R
Hydroxyl Radical 3352-57-6
Hydrogen Peroxide BBX060AN9V

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

318-324

Informations de copyright

©2022 by Radiation Research Society. All rights of reproduction in any form reserved.

Auteurs

Guillaume Blain (G)

Laboratoire SUBATECH, UMR 6457, CNRS IN2P3, IMT Atlantique, Université de Nantes, France.

Johan Vandenborre (J)

Laboratoire SUBATECH, UMR 6457, CNRS IN2P3, IMT Atlantique, Université de Nantes, France.

Daphnée Villoing (D)

Institut de Cancérologie de l'Ouest, Saint-Herblain, France.

Vincent Fiegel (V)

Institut de Cancérologie de l'Ouest, Saint-Herblain, France.

Giovanna Rosa Fois (GR)

Université Clermont Auvergne, CNRS/IN2P3, LPC, 63000 Clermont-Ferrand, France.

Ferid Haddad (F)

Laboratoire SUBATECH, UMR 6457, CNRS IN2P3, IMT Atlantique, Université de Nantes, France.
GIP ARRONAX, Saint-Herblain, France.

Charbel Koumeir (C)

GIP ARRONAX, Saint-Herblain, France.

Lydia Maigne (L)

Université Clermont Auvergne, CNRS/IN2P3, LPC, 63000 Clermont-Ferrand, France.

Vincent Métivier (V)

Laboratoire SUBATECH, UMR 6457, CNRS IN2P3, IMT Atlantique, Université de Nantes, France.

Freddy Poirier (F)

GIP ARRONAX, Saint-Herblain, France.

Vincent Potiron (V)

Institut de Cancérologie de l'Ouest, Saint-Herblain, France.

Stéphane Supiot (S)

Institut de Cancérologie de l'Ouest, Saint-Herblain, France.

Noël Servagent (N)

Laboratoire SUBATECH, UMR 6457, CNRS IN2P3, IMT Atlantique, Université de Nantes, France.

Grégory Delpon (G)

Institut de Cancérologie de l'Ouest, Saint-Herblain, France.

Sophie Chiavassa (S)

Institut de Cancérologie de l'Ouest, Saint-Herblain, France.

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Classifications MeSH