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用于硼中子俘获治疗的表皮生长因子-葡聚糖缀合物的研发及体外研究

Development and in vitro studies of epidermal growth factor-dextran conjugates for boron neutron capture therapy.

作者信息

Gedda L, Olsson P, Pontén J, Carlsson J

机构信息

Department of Diagnostic Radiology, Uppsala University, Sweden.

出版信息

Bioconjug Chem. 1996 Sep-Oct;7(5):584-91. doi: 10.1021/bc9600473.

Abstract

A delivery molecule for directed boron neutron capture therapy against epidermal growth factor (EGF) receptor-rich tumors, such as gliomas, squamous carcinomas, and breast cancers, is presented. EGF and sulfhydryl boron hydride (BSH) were covalently coupled to an allylated 70 kDa dextran chain to form a conjugate. Conjugates with low and high substitution rates of BSH, as well as without BSH, were investigated. The conjugate with a low amount of boron had approximately 6 BSH (72 boron atoms) per dextran, while the conjugates with higher amounts had an average substitution of 55 BSH (660 boron atoms) per dextran. The maximum substitution of boron to dextran in a single experiment was over 800 boron atoms. Binding, retention, and internalization of 125I-labeled conjugates were investigated on cultured human glioma cells. Binding of the conjugates was EGF receptor specific, but the amount of BSH coupled to dextran affected specificity, more than the presence of dextran. The nonspecific binding of the conjugates increased with the amount of attached boron. This was partly due to nonspecific adhesion to the plastic in the culture dishes. [125I]EGF-allyldextran with 6 BSH had a binding maximum after 4 h of continuous incubation and thereafter decreased in binding, while [125I]EGF-allyldextran with the higher substitution rate had a slow increase of binding during 24 h. Over 93% of the radioactivity bound to the cells was internalized, but the retention was quite poor. Only one-third of the cell-bound activity was still associated to the cells 4 h after incubation had ended. In conclusion, it is possible to load the conjugates produced with high amounts of boron, and they retained specificity for the EGF receptor and internalized into cultured cells. Theoretical calculations show that about 10(3) boron atoms per EGF-based conjugate are needed to give a satisfactory therapeutic response. These conjugates are within reach of that level.

摘要

本文介绍了一种用于针对富含表皮生长因子(EGF)受体的肿瘤(如神经胶质瘤、鳞状细胞癌和乳腺癌)进行定向硼中子俘获治疗的递送分子。将EGF与巯基硼氢化物(BSH)共价偶联到烯丙基化的70 kDa葡聚糖链上,形成一种共轭物。对具有低、高BSH取代率以及不含BSH的共轭物进行了研究。硼含量低的共轭物每个葡聚糖约有6个BSH(72个硼原子),而硼含量较高的共轭物平均每个葡聚糖有55个BSH(660个硼原子)。单次实验中硼对葡聚糖的最大取代量超过800个硼原子。在培养的人神经胶质瘤细胞上研究了125I标记的共轭物的结合、保留和内化情况。共轭物的结合具有EGF受体特异性,但与葡聚糖偶联的BSH量对特异性的影响大于葡聚糖的存在。共轭物的非特异性结合随附着硼的量增加而增加。这部分是由于与培养皿中的塑料发生非特异性粘附。含6个BSH的[125I]EGF - 烯丙基葡聚糖在连续孵育4小时后达到最大结合,此后结合量下降,而取代率较高的[125I]EGF - 烯丙基葡聚糖在24小时内结合量缓慢增加。与细胞结合的放射性物质中超过93%被内化,但保留情况相当差。孵育结束4小时后,只有三分之一与细胞结合的活性仍与细胞相关。总之,有可能负载大量硼产生的共轭物,它们对EGF受体保持特异性并内化到培养细胞中。理论计算表明,每个基于EGF的共轭物需要约10(3)个硼原子才能产生令人满意的治疗反应。这些共轭物已达到该水平。

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