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硼脂质体脂质体硼递药系统用于中子俘获治疗:最新进展与未来展望。

Boron lipid-based liposomal boron delivery system for neutron capture therapy: recent development and future perspective.

机构信息

Department of Chemistry, Faculty of Science, Gakushuin University, Mejiro, Toshima-ku, Tokyo.

出版信息

Future Med Chem. 2013 Apr;5(6):715-30. doi: 10.4155/fmc.13.48.

Abstract

Recent development of boron cluster lipids and their liposomal boron delivery system (BDS) are summarized in this article. Boron compounds used in boron neutron capture therapy (BNCT) are, in general, nontoxic unless neutron capture reaction of boron takes place. Therefore, the boron compounds accumulated into other organs would not cause such side effects for patient. Selective and sufficient delivery of boron-10 to tumor results in the successful BNCT. There are two approaches for BDS: encapsulation of boron compounds into liposomes and incorporation of boron-conjugated lipids into the liposomal bilayer, both of which have been significantly investigated. The combination of both approaches displayed potency and, hence, the ability to reduce the total dose of liposomes without reducing the efficacy of BNCT. Boron compounds that have no affinity to tumor can potentially be delivered to tumor tissues by liposomes, therefore, liposomal BDS would be one of the most attractive approaches for efficient BNCT of various cancers.

摘要

本文总结了硼簇脂质及其脂质体硼递药系统(BDS)的最新进展。硼中子俘获治疗(BNCT)中使用的硼化合物一般是无毒的,除非发生硼的中子俘获反应。因此,硼化合物在其他器官中的积累不会对患者造成这样的副作用。选择性和充分地将硼-10递送到肿瘤中会导致 BNCT 的成功。BDS 有两种方法:将硼化合物包封到脂质体中,以及将硼缀合脂质整合到脂质双层中,这两种方法都得到了广泛的研究。这两种方法的结合显示出了效力,因此能够在不降低 BNCT 疗效的情况下减少脂质体的总剂量。没有肿瘤亲和力的硼化合物可以通过脂质体潜在地递送到肿瘤组织中,因此,脂质体 BDS 将是各种癌症高效 BNCT 的最有吸引力的方法之一。

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