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PreprintCC BY 4.0arXiv

Using a radiopharmaceutical production cyclotron for radiobiological research

Abstract

The Laboratory for High Energy Physics and the Institute of Anatomy at the University of Bern are establishing a pre-clinical proton therapy research facility at the Bern University Hospital (Inselspital). The facility centers on the Bern Medical Cyclotron, an 18 MeV compact cyclotron designed for microampere-range beam currents for radioisotope production. The Bern Medical Cyclotron can be adapted as a highly accessible and customizable platform for pre-clinical proton therapy research, enabling advanced modalities such as ultra-high dose rate (FLASH) radiotherapy and spatially fractionated radiation therapy. Human keratinocytes (HaCaT) and mouse melanoma (B16-F10) cell lines were irradiated with 8.14(29) MeV protons at conventional dose rates and with 225 kV X-rays at doses from 0 to 8 Gy. Clonogenic survival assays were analyzed using the linear-quadratic model, and relative biological effectiveness values were derived by comparing the proton and X-ray doses required for 0.1 survival. Proton irradiation yielded steeper survival curves than X-rays, indicating higher cytotoxicity. B16-F10 cells were most sensitive, with a relative biological effectiveness of 1.34 at 0.1 survival, while HaCaT cells showed a relative biological effectiveness of 1.21. These results confirm enhanced proton effectiveness in cell killing and demonstrate that the Bern Medical Cyclotron provides a reliable platform for radiobiological studies. Establishing in vitro proton irradiation capability marks a key milestone toward developing a comprehensive pre-clinical radiobiology research facility in Bern. Ongoing upgrades will further refine dosimetry and proton delivery, paving the way for future FLASH and proton spatially fractionated radiation therapy studies.

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BibTeX
@misc{kasanda2026using,
  title = {{Using a radiopharmaceutical production cyclotron for radiobiological research}},
  author = {Eva Kasanda and Jan Gruber and Pierluigi Casolaro and Lars Eggimann and Alexander Gottstein and Isidre Mateu and Paolo Pellicioli and Maria Vittoria Rossi and Paola Scampoli and Cristian Fernandez-Palomo and Saverio Braccini},
  howpublished = {arXiv},
  year = {2026},
  month = sep,
  doi = {10.48550/arxiv.2609.37623},
  eprint = {2609.37623},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2609.37623},
  note = {CC BY 4.0},
}
RIS
TY  - UNPB
TI  - Using a radiopharmaceutical production cyclotron for radiobiological research
AU  - Eva Kasanda
AU  - Jan Gruber
AU  - Pierluigi Casolaro
AU  - Lars Eggimann
AU  - Alexander Gottstein
AU  - Isidre Mateu
AU  - Paolo Pellicioli
AU  - Maria Vittoria Rossi
AU  - Paola Scampoli
AU  - Cristian Fernandez-Palomo
AU  - Saverio Braccini
PY  - 2026
DA  - 2026/09/29
PB  - arXiv
DO  - 10.48550/arxiv.2609.37623
UR  - https://arxiv.org/abs/2609.37623
AB  - The Laboratory for High Energy Physics and the Institute of Anatomy at the University of Bern are establishing a pre-clinical proton therapy research facility at the Bern University Hospital (Inselspital). The facility centers on the Bern Medical Cyclotron, an 18 MeV compact cyclotron designed for microampere-range beam currents for radioisotope production. The Bern Medical Cyclotron can be adapted as a highly accessible and customizable platform for pre-clinical proton therapy research, enabling advanced modalities such as ultra-high dose rate (FLASH) radiotherapy and spatially fractionated radiation therapy. Human keratinocytes (HaCaT) and mouse melanoma (B16-F10) cell lines were irradiated with 8.14(29) MeV protons at conventional dose rates and with 225 kV X-rays at doses from 0 to 8 Gy. Clonogenic survival assays were analyzed using the linear-quadratic model, and relative biological effectiveness values were derived by comparing the proton and X-ray doses required for 0.1 survival. Proton irradiation yielded steeper survival curves than X-rays, indicating higher cytotoxicity. B16-F10 cells were most sensitive, with a relative biological effectiveness of 1.34 at 0.1 survival, while HaCaT cells showed a relative biological effectiveness of 1.21. These results confirm enhanced proton effectiveness in cell killing and demonstrate that the Bern Medical Cyclotron provides a reliable platform for radiobiological studies. Establishing in vitro proton irradiation capability marks a key milestone toward developing a comprehensive pre-clinical radiobiology research facility in Bern. Ongoing upgrades will further refine dosimetry and proton delivery, paving the way for future FLASH and proton spatially fractionated radiation therapy studies.
ER  -