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一种用于硼化抗体且不丧失免疫反应性的新方法,用于中子俘获治疗。

A novel method for boronating antibodies without loss of immunoreactivity, for use in neutron capture therapy.

作者信息

Ferro V A, Morris J H, Stimson W H

机构信息

Department of Immunology, University of Strathclyde, Todd Centre, Glasgow, UK.

出版信息

Drug Des Discov. 1995 Aug;13(1):13-25.

PMID:8882898
Abstract

The search for suitable boron containing compounds for 10B neutron capture therapy (BNCT) is based on the principle that boron atoms must be delivered specifically to tumour cells at a concentration high enough to be effective without being toxic to normal cells. Specificity may be achieved through monoclonal antibodies. However, it has been difficult to conjugate large numbers of boron atoms to the antibody molecules without inactivating them. We have devised a strategy to do this indirectly through the use of a boronated glutamate-lysine polymer in conjunction with biotin and streptavidin.

摘要

寻找适用于硼中子俘获疗法(BNCT)的含硼化合物是基于这样的原则:硼原子必须以足够高的浓度特异性地输送到肿瘤细胞中,以达到有效治疗的目的,同时又不会对正常细胞产生毒性。特异性可以通过单克隆抗体来实现。然而,在不使抗体分子失活的情况下,将大量硼原子与抗体分子结合一直很困难。我们设计了一种策略,通过使用硼化谷氨酸 - 赖氨酸聚合物结合生物素和链霉亲和素来间接实现这一目标。

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