Modelling Potential Candidates for Targeted Auger Therapy

Targeted Auger emitters are being considered as a cancer treatment owing to the high linear energy transfer of Auger electrons. When targeted to cancers, this allows for a highly efficient treatment with a low risk of damage to surrounding healthy tissue. The purpose of this study was to determine t...

Full description

Saved in:
Bibliographic Details
Main Authors: Conor M. J. Buchanan, Eric O. Aboagye, Lee J. Evitts, Michael J. D. Rushton, Tim A. D. Smith
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Biophysica
Subjects:
Online Access:https://www.mdpi.com/2673-4125/4/4/46
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850240288321175552
author Conor M. J. Buchanan
Eric O. Aboagye
Lee J. Evitts
Michael J. D. Rushton
Tim A. D. Smith
author_facet Conor M. J. Buchanan
Eric O. Aboagye
Lee J. Evitts
Michael J. D. Rushton
Tim A. D. Smith
author_sort Conor M. J. Buchanan
collection DOAJ
description Targeted Auger emitters are being considered as a cancer treatment owing to the high linear energy transfer of Auger electrons. When targeted to cancers, this allows for a highly efficient treatment with a low risk of damage to surrounding healthy tissue. The purpose of this study was to determine the most DNA-damaging Auger emitters from a range of radionuclides, some of which are clinically utilised. A Monte Carlo method-based software (Geant4-DNA version 10.7) was used to determine the energy deposition and number of DNA double-strand breaks from Auger (and internal conversion) electrons imposed on a tetranucleosome. The Auger emitters, <sup>119</sup>Sb and <sup>103</sup>Pd, have similar or slightly greater damaging properties compared to <sup>123</sup>I, <sup>111</sup>In, and <sup>89</sup>Zr. <sup>193m</sup>Pt demonstrated the greatest therapeutic potency. Whilst <sup>125</sup>I was highly damaging, its relatively long half-life (60 days) makes it less desirable for clinical use. Geant4-DNA modelling identified the radionuclide <sup>193m</sup>Pt as being highly favourable for use in radiotherapy.
format Article
id doaj-art-37043c23340646d4bc2b57ad08bfcd4e
institution OA Journals
issn 2673-4125
language English
publishDate 2024-12-01
publisher MDPI AG
record_format Article
series Biophysica
spelling doaj-art-37043c23340646d4bc2b57ad08bfcd4e2025-08-20T02:00:54ZengMDPI AGBiophysica2673-41252024-12-014471172310.3390/biophysica4040046Modelling Potential Candidates for Targeted Auger TherapyConor M. J. Buchanan0Eric O. Aboagye1Lee J. Evitts2Michael J. D. Rushton3Tim A. D. Smith4Nuclear Futures Institute, Bangor University, Gwynedd LL57 2DG, UKDepartment of Surgery and Cancer, Faculty of Medicine, Commonwealth Building, Hammersmith Campus, Imperial College London, London W12 0NN, UKNuclear Futures Institute, Bangor University, Gwynedd LL57 2DG, UKNuclear Futures Institute, Bangor University, Gwynedd LL57 2DG, UKNuclear Futures Institute, Bangor University, Gwynedd LL57 2DG, UKTargeted Auger emitters are being considered as a cancer treatment owing to the high linear energy transfer of Auger electrons. When targeted to cancers, this allows for a highly efficient treatment with a low risk of damage to surrounding healthy tissue. The purpose of this study was to determine the most DNA-damaging Auger emitters from a range of radionuclides, some of which are clinically utilised. A Monte Carlo method-based software (Geant4-DNA version 10.7) was used to determine the energy deposition and number of DNA double-strand breaks from Auger (and internal conversion) electrons imposed on a tetranucleosome. The Auger emitters, <sup>119</sup>Sb and <sup>103</sup>Pd, have similar or slightly greater damaging properties compared to <sup>123</sup>I, <sup>111</sup>In, and <sup>89</sup>Zr. <sup>193m</sup>Pt demonstrated the greatest therapeutic potency. Whilst <sup>125</sup>I was highly damaging, its relatively long half-life (60 days) makes it less desirable for clinical use. Geant4-DNA modelling identified the radionuclide <sup>193m</sup>Pt as being highly favourable for use in radiotherapy.https://www.mdpi.com/2673-4125/4/4/46radionuclidetargetedaugercancer
spellingShingle Conor M. J. Buchanan
Eric O. Aboagye
Lee J. Evitts
Michael J. D. Rushton
Tim A. D. Smith
Modelling Potential Candidates for Targeted Auger Therapy
Biophysica
radionuclide
targeted
auger
cancer
title Modelling Potential Candidates for Targeted Auger Therapy
title_full Modelling Potential Candidates for Targeted Auger Therapy
title_fullStr Modelling Potential Candidates for Targeted Auger Therapy
title_full_unstemmed Modelling Potential Candidates for Targeted Auger Therapy
title_short Modelling Potential Candidates for Targeted Auger Therapy
title_sort modelling potential candidates for targeted auger therapy
topic radionuclide
targeted
auger
cancer
url https://www.mdpi.com/2673-4125/4/4/46
work_keys_str_mv AT conormjbuchanan modellingpotentialcandidatesfortargetedaugertherapy
AT ericoaboagye modellingpotentialcandidatesfortargetedaugertherapy
AT leejevitts modellingpotentialcandidatesfortargetedaugertherapy
AT michaeljdrushton modellingpotentialcandidatesfortargetedaugertherapy
AT timadsmith modellingpotentialcandidatesfortargetedaugertherapy