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neutron capture therapy中文是什么意思

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用"neutron capture therapy"造句"neutron capture therapy"怎么读"neutron capture therapy" in a sentence

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  • 中子俘获治疗法

例句与用法

  • Neutron capture therapy ; liposome ; gadolinium complex ; tumor cell
    中子俘获治疗脂质体钆配合物癌细胞
  • Transport of liposome as a carrier for gadolinium neutron capture therapy
    脂质体作为钆中子俘获治疗肿瘤药物载体的
  • Kinetics and mechanism study of across - membrane transport of liposome as a carrier for gadolinium neutron capture therapy
    脂质体作为钆中子俘获治疗肿瘤药物载体的跨膜动力学及机理研究
  • In recent years , study of boron neutron capture therapy has been aimed at the establishment of epithermal neutron beams in order to avoid the open - skull surgury and for the treatment of deep - seated tumors
    摘要近年来，硼中子捕捉治疗之研究倾向于采用超热中子束以避免切开头盖骨之手术及进行较深层之肿瘤治疗。
  • From 1950s to 1980s , the ( superscript 10 ) b - neutron capture therapy ( bnct ) has been considered as an effective and useful treatment modality for some kinds of cancer through a series of testing work
    摘要自1950年代到1980年代，硼捉中子治疗模式经过种种的试验阶段，其临床实用性终于在某些癌病的治疗上获得初步证实。
  • Liposome is an effective nuclide delivery agent for neutron capture therapy . in this paper liposomes containing encapsulated gadolinium complex were prepared and characterized . the influence of formulation factors such as ph , ionic strength , buffer , and storage time upon the stability of liposomes was investigated . the uptake rate constant and its concentration dependence of lgd in tumor cells were compared in vitro with that of gd complex itself . the results indicate that the uptake rate of lgd in tumor cells increases to eight times as much as that of gd - edta , but the release rate of gd from tumor cells containing lgd is remarkably lower than that from the tumor cells containing gd - edta . the results reveal that lgd would be a potential drug for neutron capture therapy of cancer
    制备和表征了包埋gd - edta的脂质体，测定了ph ，离子强度，缓冲液组成及温度对gd - edta脂质体的影响，比较了gd - edta脂质体和gd - edta被肿瘤细胞摄入的动力学曲线。结果表明， gd - edta脂质体在37和生理条件下最稳定，肿瘤细胞摄入gd - edta脂质体速率是gd - edta的8倍，而释放gd的速率， gd - edta脂质体远远低于gd - edta ,这些结果提供了脂质体包埋gd - edta作为钆中子俘获治疗药物的可能性。
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