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

机译:新型硼试剂和基于加速器中子源的硼中子捕获治疗(BNCT)的基本研究

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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:最近癌症案例的数量一直在增加。此外,由于人口老龄化,人们之间的数量多样化,因此需要对肿瘤的较少侵入性和高QOL(生活质量)治疗。 BNCT(硼中子捕获疗法)基于两个基本上无毒物种,<0b和热中子的核反应。 BNCT是有效和微创的治疗。然而,BNCT效率低下,因为原子反应器用于中子源。在这项研究中,我们向BNCT使用加速器和新的硼剂; HVJ(日本的He-Magglutination病毒)包络(HVJ-E)和硼润脂质体(B-脂质体)。 HVJ-E是使用灭活病毒颗粒的非血流量载体,它可以通过膜沉默活性衍生成细胞。 B-脂质体由硼酸化磷三磷酯类似物制成,可以将包封在用硼脂质体中的药物。我们尝试使用加速器和新药物在体内进行BNCT TRAIL。我们使用了A549细胞系和OKTavian,D-T反应是14 Mev中子源。结果,与常规硼化合物(硼丙酸钠:BSH)相比,这些新硼试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的BNCT的可能性。

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