Comparison of Radionuclide Drug Conjugates With Boron Neutron Capture Therapy: An Overview of Targeted Charged Particle Radiation Therapy.

IF 10.9 1区 医学 Q1 CHEMISTRY, MEDICINAL
Yingjun Zhang, Paolo Coghi, Zimo Ren, Narayan S Hosmane, Yinghuai Zhu
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引用次数: 0

Abstract

Targeted charged alpha- and beta-particle therapies are currently being used in clinical radiation treatments as newly developed methods for either killing or controlling tumor cell growth. The alpha particles can be generated either through a nuclear decay reaction or in situ by a nuclear fission reaction such as the boron neutron capture reaction. Different strategies have been employed to improve the selectivity and delivery of radiation dose to tumor cells based on the source of the clinically used alpha particles. As a result, the side effects of the treatment can be minimized. The increasing attention and research efforts on targeted alpha-particle therapy have been fueled by exciting results of both academic research and clinical trials. It is highly anticipated that alpha-particle therapy will improve the efficacy of treating malignant tumors. In this overview, we compare radionuclide drug conjugates (RDC) with boron neutron capture therapy (BNCT) to present recent developments in targeted alpha-particle therapy.

放射性核素药物偶联物与硼中子俘获治疗的比较:靶向带电粒子放射治疗综述。
靶向带电α粒子和β粒子疗法作为一种新开发的杀死或控制肿瘤细胞生长的方法,目前被用于临床放射治疗。α粒子既可以通过核衰变反应产生,也可以通过核裂变反应(如硼中子捕获反应)就地产生。根据临床使用的α粒子的来源,采用了不同的策略来提高肿瘤细胞辐射剂量的选择性和递送。因此,治疗的副作用可以降到最低。学术研究和临床试验的令人兴奋的结果推动了对靶向α粒子治疗的日益关注和研究努力。粒子疗法有望提高恶性肿瘤的治疗效果。在这篇综述中,我们比较了放射性核素药物偶联物(RDC)和硼中子俘获治疗(BNCT),以介绍靶向α粒子治疗的最新进展。
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来源期刊
CiteScore
29.30
自引率
0.00%
发文量
52
审稿时长
2 months
期刊介绍: Medicinal Research Reviews is dedicated to publishing timely and critical reviews, as well as opinion-based articles, covering a broad spectrum of topics related to medicinal research. These contributions are authored by individuals who have made significant advancements in the field. Encompassing a wide range of subjects, suitable topics include, but are not limited to, the underlying pathophysiology of crucial diseases and disease vectors, therapeutic approaches for diverse medical conditions, properties of molecular targets for therapeutic agents, innovative methodologies facilitating therapy discovery, genomics and proteomics, structure-activity correlations of drug series, development of new imaging and diagnostic tools, drug metabolism, drug delivery, and comprehensive examinations of the chemical, pharmacological, pharmacokinetic, pharmacodynamic, and clinical characteristics of significant drugs.
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