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Laser driven FLASH radiobiology using a high dose and ultra high dose rate single pulse proton source

  • A. Flacco
  • , E. Bayart
  • , L. Romagnani
  • , M. Cavallone
  • , L. De Marzi
  • , C. Fouillade
  • , C. Giaccaglia
  • , S. Heinrich
  • , I. Lamarre-Jouenne
  • , J. Monzac
  • , K. Parodi
  • , A. Patriarca
  • , T. Rösch
  • , J. Schreiber
  • , L. Tischendorf
  • Laboratory d'Optique Appliquée, ENSTA, CNRS-École Polytechnique
  • Institut Curie
  • Université Paris-Saclay
  • Institut Polytechnique de Paris
  • Universität München

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

Résumé

Laser-driven proton sources have long been developed with an eye on their potential for medical application to radiation therapy. These sources are compact, versatile, and show peculiar characteristics such as extreme instantaneous dose rates, short duration and broad energy spectrum. Typical temporal modality of laser-driven irradiation, the so-called fast-fractionation, results from the composition of multiple, temporally separated, ultra-short dose fractions. In this paper we present the use of a high-energy laser system for delivering the target dose in a single nanosecond pulse, for ultra-fast irradiation of biological samples. A transport line composed by two permanent-magnet quadrupoles and a scattering system is used to improve the dose profile and to control the delivered dose-per-pulse. A single-shot dosimetry protocol for the broad-spectrum proton source using Monte Carlo simulations was developed. Doses as high as 20 Gy could be delivered in a single shot, lasting less than 10 ns over a 1 cm diameter biological sample, at a dose-rate exceeding. Exploratory application of extreme laser-driven irradiation conditions, falling within the FLASH irradiation protocol, are presented for irradiation in vitro and in vivo. A reduction of radiation-induced oxidative stress in vitro and radiation-induced developmental damage compatible with the onset of FLASH effect were observed in vivo, whereas anti-tumoral efficacy was confirmed by cell survival assay.

langue originaleAnglais
Numéro d'article16511
journalScientific Reports
Volume15
Numéro de publication1
Les DOIs
étatPublié - 1 déc. 2025

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