4.6 Article

Investigation of gold nanoparticle radiosensitization mechanisms using a free radical scavenger and protons of different energies

Journal

PHYSICS IN MEDICINE AND BIOLOGY
Volume 59, Issue 21, Pages 6431-6443

Publisher

IOP Publishing Ltd
DOI: 10.1088/0031-9155/59/21/6431

Keywords

protons; x-rays; clonogenic assays; gold nanoparticles; radiosensitization; Geant4

Funding

  1. Marie Curie Actions - Initial Training Networks (ITN) as an Integrating Activity Supporting Postgraduate Research with Internships in Industry and Training Excellence (SPRITE) under EC [317169]
  2. European Community as an Integrating Activity 'Support of Public and Industrial Research Using Ion Beam Technology (SPIRIT)' under EC [227012]
  3. SPRITE
  4. UK EPSRC [EP/C009592/1]
  5. Engineering and Physical Sciences Research Council [EP/D032210/1, EP/C009592/1] Funding Source: researchfish
  6. EPSRC [EP/C009592/1, EP/D032210/1] Funding Source: UKRI

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Gold nanoparticles (GNPs) have been shown to sensitize cancer cells to x-ray radiation, particularly at kV energies where photoelectric interactions dominate and the high atomic number of gold makes a large difference to x-ray absorption. Protons have a high cross-section for gold at a large range of relevant clinical energies, and so potentially could be used with GNPs for increased therapeutic effect. Here, we investigate the contribution of secondary electron emission to cancer cell radiosensitization and investigate how this parameter is affected by proton energy and a free radical scavenger. We simulate the emission from a realistic cell phantom containing GNPs after traversal by protons and x-rays with different energies. We find that with a range of proton energies (1-250 MeV) there is a small increase in secondaries compared to a much larger increase with x-rays. Secondary electrons are known to produce toxic free radicals. Using a cancer cell line in vitro we find that a free radical scavenger has no protective effect on cells containing GNPs irradiated with 3 MeV protons, while it does protect against cells irradiated with x-rays. We conclude that GNP generated free radicals are a major cause of radiosensitization and that there is likely to be much less dose enhancement effect with clinical proton beams compared to x-rays.

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