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电穿孔对使用硼卡醇钠(10B-BSH)的硼中子俘获疗法细胞杀伤的影响。

Effect of electroporation on cell killing by boron neutron capture therapy using borocaptate sodium (10B-BSH).

作者信息

Ono K, Kinashi Y, Masunaga S, Suzuki M, Takagaki M

机构信息

Radiation Oncology Research Laboratory, Kyoto University, Osaka.

出版信息

Jpn J Cancer Res. 1998 Dec;89(12):1352-7. doi: 10.1111/j.1349-7006.1998.tb00533.x.

Abstract

The cell membrane permeability of 10B-enriched borocaptate sodium (BSH) and the extent to which BSH is accumulated in cells are controversial. To elucidate these points and to enhance the accumulation of BSH in cells, the effect of electroporation on boron neutron capture therapy (BNCT) using BSH was investigated. The first group of SCCVII tumor cells was incubated in culture medium with 10B-BSH or 10B-enriched boric acid, and exposed to neutrons from the heavy water facility of the Kyoto University Reactor. More than 99% of neutrons were thermal neutrons at flux base. The second group was pretreated with electroporation in combination with 10B-BSH, and thereafter the cells were irradiated with neutrons. The cell-killing effect of BNCT was measured by colony formation assay. The surviving cell fraction decreased exponentially with neutron fluence, and addition of BSH significantly enhanced the cell-killing effect of NCT depending on 10B concentration and the preincubation time of cells in the BSH-containing culture medium. The electroporation of cells with BSH markedly enhanced the BNCT effect in comparison with that obtained with preincubation alone. The effect of BSH-BNCT with electroporation was almost equal to that of BNCT using 10B-boric acid at the same 10B concentration. The effect of BNCT on cells pretreated with BSH and electroporation was not reduced by repeated washing of the cells before neutron irradiation. Decrease of the effect of BSH-BNCT plus electroporation with increase in the waiting time between the electroporation and the neutron irradiation could be explained in terms of the extent of cell growth during that time. These data suggest that BSH penetrates the cells slowly and remains after washing. Electroporation can introduce BSH into the cells very efficiently, and BSH thus introduced stays in the cells and is not lost in spite of the intensive washing of the cells. Therefore, if electroporation is applied to tumors after BSH injection, 10B would remain in the tumors but be cleared from normal tissues, and selective accumulation of 10B in tumors will be achieved after an appropriate waiting time.

摘要

富集硼的硼卡醇钠(BSH)的细胞膜通透性以及BSH在细胞中的积累程度存在争议。为了阐明这些问题并增强BSH在细胞中的积累,研究了电穿孔对使用BSH的硼中子俘获疗法(BNCT)的影响。第一组SCCVII肿瘤细胞在含有10B-BSH或富集10B的硼酸的培养基中孵育,并暴露于京都大学反应堆重水设施产生的中子。在通量基准下,超过99%的中子是热中子。第二组先用10B-BSH结合电穿孔进行预处理,然后对细胞进行中子照射。通过集落形成试验测量BNCT的细胞杀伤效果。存活细胞分数随中子注量呈指数下降,添加BSH显著增强了NCT的细胞杀伤效果,这取决于10B浓度和细胞在含BSH培养基中的预孵育时间。与单独预孵育相比,用BSH对细胞进行电穿孔显著增强了BNCT效果。在相同的10B浓度下,电穿孔的BSH-BNCT效果几乎与使用10B-硼酸的BNCT效果相同。在中子照射前对细胞进行反复洗涤,不会降低BSH和电穿孔预处理对细胞的BNCT效果。随着电穿孔和中子照射之间等待时间的增加,BSH-BNCT加电穿孔效果的降低可以用这段时间内细胞生长的程度来解释。这些数据表明,BSH缓慢穿透细胞并在洗涤后留存。电穿孔可以非常有效地将BSH引入细胞,并且如此引入的BSH留在细胞中,即使对细胞进行大量洗涤也不会丢失。因此,如果在注射BSH后对肿瘤施加电穿孔,10B将保留在肿瘤中,但从正常组织中清除,并且在适当的等待时间后将实现10B在肿瘤中的选择性积累。

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