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Basic investigation of boron neutron capture therapy (BNCT) using novel boron agents and accelerator based neutron source

机译:使用新型硼剂和基于加速器的中子源进行硼中子俘获疗法(BNCT)的基础研究

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Recently the number of cancer case has been increasing. In addition, because of aging of the population and diversification of values among the people, less-invasive and high-QOL (quality of life) treatment for tumors has been needed. BNCT (Boron Neutron Capture Therapy) is based on the nuclear reaction of two essentially nontoxic species, <0B and thermal neutron. BNCT is effective and minimally invasive treatment. However BNCT is inefficient because atomic reactor is used for neutron source. In this study, we proposed to BNCT using an accelerator and new boron agents; HVJ (He-magglutinating Virus of Japan) envelope (HVJ-E) and Boro-nated liposome (B-Liposome). HVJ-E is a nonviral vector using inactivated virus particle and it can deriver inclusions into cells via membrane-fusing activity. B-Liposome made of boronated phosphatide analogue can deliver the drug which is encapsulated into liposome with boron. We tried BNCT trail in vivo using an accelerator and new drugs. We used A549 cell line and OKTAVIAN which is 14 MeV neutron source by D-T reaction. In the result, these new boron agents realized the sufficient intracellular boron concentration and higher cyto-toxicity reaction compared with a conventional boron compound (Sodium borocaptate: BSH). Therefore, we confirmed the possibility of BNCT using new drugs.
机译:最近,癌症病例的数量一直在增加。另外,由于人口的老龄化和人们价值观念的多样化,需要对肿瘤进行低侵入性和高QOL(生活质量)的治疗。 BNCT(硼中子捕获疗法)基于两种基本无毒的物质(<0B和热中子)的核反应。 BNCT是有效的微创治疗。但是,BNCT效率低下,因为原子反应堆用于中子源。在这项研究中,我们向BNCT提出了使用促进剂和新型硼剂的建议。 HVJ(日本的血凝病毒)包膜(HVJ-E)和硼化脂质体(B-脂质体)。 HVJ-E是使用灭活病毒颗粒的非病毒载体,它可以通过膜融合活性将包涵体衍生到细胞中。由硼化的磷脂类似物制成的B-脂质体可以递送与硼一起包裹在脂质体中的药物。我们使用促进剂和新药在体内尝试了BNCT踪迹。通过D-T反应,我们使用了A549细胞系和14 MeV中子源的OKTAVIAN。结果,与常规的硼化合物(硼cap酸钠:BSH)相比,这些新的硼剂实现了足够的细胞内硼浓度和更高的细胞毒性反应。因此,我们确认了使用新药进行BNCT的可能性。

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