Luderer Micah John, de la Puente Pilar, Azab Abdel Kareem
Department of Radiation Oncology, Cancer Biology Division, Washington University in Saint Louis School of Medicine, 4511 Forest Park Ave., Room 3103, St. Louis, Missouri, 63108, USA.
Pharm Res. 2015 Sep;32(9):2824-36. doi: 10.1007/s11095-015-1718-y. Epub 2015 Jun 2.
Boron neutron capture therapy (BNCT) is a promising cancer therapy modality that utilizes the nuclear capture reaction of epithermal neutrons by boron-10 resulting in a localized nuclear fission reaction and subsequent cell death. Since cellular destruction is limited to approximately the diameter of a single cell, primarily only cells in the neutron field with significant boron accumulation will be damaged. However, the emergence of BNCT as a prominent therapy has in large part been hindered by a paucity of tumor selective boron containing agents. While L-boronophenylalanine and sodium borocaptate are the most commonly investigated clinical agents, new agents are desperately needed due to their suboptimal tumor selectivity. This review will highlight the various strategies to improve tumor boron delivery including: nucleoside and carbohydrate analogs, unnatural amino acids, porphyrins, antibody-dendrimer conjugates, cationic polymers, cell-membrane penetrating peptides, liposomes and nanoparticles.
硼中子俘获疗法(BNCT)是一种很有前景的癌症治疗方式,它利用硼 - 10对超热中子的核俘获反应,产生局部核裂变反应并随后导致细胞死亡。由于细胞破坏仅限于单个细胞的直径大小,主要只有中子场中硼大量蓄积的细胞会受到损伤。然而,肿瘤选择性含硼剂的匮乏在很大程度上阻碍了BNCT成为一种卓越的治疗方法。虽然L - 硼苯丙氨酸和硼卡钠是最常研究的临床药物,但由于它们的肿瘤选择性欠佳,迫切需要新型药物。本综述将重点介绍改善肿瘤硼递送的各种策略,包括:核苷和碳水化合物类似物、非天然氨基酸、卟啉、抗体 - 树枝状聚合物缀合物、阳离子聚合物、细胞膜穿透肽、脂质体和纳米颗粒。