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Boron agents for neutron capture therapy

https://repo.qst.go.jp/records/78130
https://repo.qst.go.jp/records/78130
5f9cae50-4d80-4ca0-b575-65ccc3c3dc8e
Item type 学術雑誌論文 / Journal Article(1)
公開日 2019-12-20
タイトル
タイトル Boron agents for neutron capture therapy
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Kuan, Hu

× Kuan, Hu

WEKO 997502

Kuan, Hu

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Yang, Zhimin

× Yang, Zhimin

WEKO 997503

Yang, Zhimin

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Zhang, Lingling

× Zhang, Lingling

WEKO 997504

Zhang, Lingling

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Xie, Lin

× Xie, Lin

WEKO 997505

Xie, Lin

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Lu, Wang

× Lu, Wang

WEKO 997506

Lu, Wang

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Xu, Hao

× Xu, Hao

WEKO 997507

Xu, Hao

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Josephson, Lee

× Josephson, Lee

WEKO 997508

Josephson, Lee

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Liang, Huan

× Liang, Huan

WEKO 997509

Liang, Huan

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Ming-Rong, Zhang

× Ming-Rong, Zhang

WEKO 997510

Ming-Rong, Zhang

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Kuan, Hu

× Kuan, Hu

WEKO 997511

en Kuan, Hu

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Yang, Zhimin

× Yang, Zhimin

WEKO 997512

en Yang, Zhimin

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Lin, Xie

× Lin, Xie

WEKO 997513

en Lin, Xie

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Lu, Wang

× Lu, Wang

WEKO 997514

en Lu, Wang

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Liang, Huan

× Liang, Huan

WEKO 997515

en Liang, Huan

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Zhang, Ming-Rong

× Zhang, Ming-Rong

WEKO 997516

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抄録
内容記述タイプ Abstract
内容記述 Boron neutron capture therapy (BNCT) is a potential cancer radiotherapeutic modality, which takes advantage of the neutron capture response that occurs when boron (10B) is struck by low-energy thermal neutrons, triggering a nuclear fission reaction that ultimately causes cell death. Because the fatal radiation is restricted to approximately a single cell diameter, only cells with significant boron accumulation that are in the neutron field will be destroyed. Tumor-targeted 10B delivery agents are an essential component of BNCT. Currently, two low molecular weight boron-containing compounds, sodium mercaptoundecahydro-closo-dodecaborate (BSH) and borylphenylalanine (BPA), are mainly used in BNCT. Although both have suboptimal tumor selectivity, they have shown some therapeutic effect in patients with high-grade gliomas and several other kinds of tumors. In order to improve the efficacy of BNCT, significant effort has been devoted to developing new boron delivery agents that possess better uptake and favorable pharmacokinetic characteristics for clinical use. This review focuses on various boron delivery agents that have been developed over the past 40 years, including boron-containing amino acids, boron-containing compound conjugated-nucleosides, porphyrin derivatives, peptides, monoclonal antibodies, and different types of nanomaterials for 10B delivery. The principles underlying BNCT and the clinical trials with BNCT are briefly introduced in the first part of this review. In the second part, we provide a detailed overview of various boron delivery agents and discuss their merits and limitations. Additionally, the preclinical outcomes of these agents are included in this review and the most promising delivery agents are highlighted and compared. In summary, this article provides an overview of boron delivery agents, and critically analyzes their clinical prospects, from the view of medicinal chemists and nuclear medicine physicians.
書誌情報 Coordination Chemistry Reviews

巻 405, p. 213139, 発行日 2019-12
出版者
出版者 Elsevier
ISSN
収録物識別子タイプ ISSN
収録物識別子 0010-8545
DOI
識別子タイプ DOI
関連識別子 10.1016/j.ccr.2019.213139
関連サイト
識別子タイプ URI
関連識別子 https://www.sciencedirect.com/science/article/abs/pii/S0010854519304916
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