ID | 65299 |
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Author |
Shigehira, Takafumi
Department of Cellular Physiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Hanafusa, Tadashi
Neutron Therapy Research Center, Okayama University
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Kasai, Tomonari
Neutron Therapy Research Center, Okayama University
Furuya, Shuichi
Research Laboratory of Accelerator-Based BNCT system, Graduate School of Engineering Nagoya University
Nishimori, Hisakazu
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama 700–8558 Japan
Maeda, Yoshinobu
Department of Hematology and Oncology, Okayama University Hospital
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Michiue, Hiroyuki
Neutron Therapy Research Center, Okayama University
Fujimura, Atsushi
Department of Cellular Physiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
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Abstract | Boron neutron capture therapy (BNCT) is a radiation therapy that selectively kills cancer cells at the cellular level using the boron neutron capture reaction (BNCR) (10B(n.α)7Li). The amount of boron 10B delivers in boronophenylalanine (BPA)-BNCT to achieve anti-tumor effects is ≈15–40 ppm. The same is true for all boron drugs; however, whether the same amount of 10B is required for other boron drugs with different accumulation characteristics has not been intensively investigated. Therefore, herein, a virtual cell model with intracellular organelles is prepared, and the BPA equivalent dose concentration to the cell nucleus is analyzed using particle and heavy ion transport code system-based microdosimetry. Additionally, the intranuclear minimal region (IMR) is set as a reference for the concept of the intranuclear domain in the microdosimetric kinetic model, and the BPA equivalent dose concentration to the IMR is estimated. The required boron delivery dose greatly varies depending on the dose assessment based on the accumulation characteristics of boron agents in intracellular organelles. Evaluation of the BNCR effect according to the accumulation characteristics without being influenced by the specified value of 15–40 ppm is recommended.
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Keywords | boron agents
boron neutron capture therapy
simulation study
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Note | This is the peer reviewed version of the following article: T. Shigehira, T. Hanafusa, K. Igawa, T. Kasai, S. Furuya, H. Nishimori, Y. Maeda, H. Michiue, A. Fujimura, Particle and Heavy Ion Transport Code System-Based Microdosimetry for the Development of Boron Agents for Boron Neutron Capture Therapy. Adv. Theory Simul. 2023, 6, 2300163. https://doi.org/10.1002/adts.202300163, which has been published in final form at https://doi.org/10.1002/adts.202300163. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.
This fulltext file will be available in Apr. 2024.
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Published Date | 2023-04-28
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Publication Title |
Advanced Theory and Simulations
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Volume | volume6
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Issue | issue7
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Publisher | Wiley
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Start Page | 2300163
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ISSN | 2513-0390
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Content Type |
Journal Article
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language |
English
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OAI-PMH Set |
岡山大学
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Copyright Holders | © 2023 Wiley-VCH GmbH
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File Version | author
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DOI | |
Web of Science KeyUT | |
Related Url | isVersionOf https://doi.org/10.1002/adts.202300163
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Citation | T. Shigehira, T. Hanafusa, K. Igawa, T. Kasai, S. Furuya, H. Nishimori, Y. Maeda, H. Michiue, A. Fujimura, Particle and Heavy Ion Transport Code System-Based Microdosimetry for the Development of Boron Agents for Boron Neutron Capture Therapy. Adv. Theory Simul. 2023, 6, 2300163. https://doi.org/10.1002/adts.202300163
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Funder Name |
Japan Society for the Promotion of Science
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助成番号 | JP21K07730
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