Department of Chemistry 'Ugo Schiff' & CSGI, University of Florence, Florence, Italy.
Int J Pharm. 2013 Dec 31;458(2):340-6. doi: 10.1016/j.ijpharm.2013.10.008. Epub 2013 Oct 16.
In this paper we propose a bottom-up approach to obtain new boron carriers built with ortho-carborane functionalized gold nanoparticles (GNPs) for applications in Boron Neutron Capture Therapy. The interaction between carboranes and the gold surface was assured by one or two SH-groups directly linked to the boron atoms of the B10C2 cage. This allowed obtaining stable, nontoxic systems, though optimal biological performance was hampered by low solubility in aqueous media. To improve cell uptake, the hydrophilic character of carborane functionalized GNPs was enhanced by further coverage with an appropriately tailored diblock copolymer (PEO-b-PCL). This polymer also contained pendant carboranes to provide anchoring to the pre-functionalized GNPs. In vitro tests, carried out on osteosarcoma cells, showed that the final vectors possessed excellent biocompatibility joint to the capacity of concentrating boron atoms in the target, which is encouraging evidenced to pursue applications in vivo.
在本文中,我们提出了一种自下而上的方法,以获得新的硼载体,这些载体由具有正-方硼烷官能化的金纳米粒子(GNPs)构建,用于硼中子俘获治疗。通过一个或两个直接与 B10C2笼的硼原子相连的 SH 基团,确保了方硼烷与金表面的相互作用。这允许获得稳定、无毒的系统,尽管由于在水介质中的低溶解度,最佳的生物性能受到阻碍。为了提高细胞摄取,通过进一步覆盖具有适当剪裁的两亲嵌段共聚物(PEO-b-PCL)来增强硼功能化 GNPs 的亲水性。该聚合物还含有侧挂的方硼烷,以提供对预官能化 GNPs 的锚固。在骨肉瘤细胞上进行的体外测试表明,最终载体具有优异的生物相容性,并且能够将硼原子集中在靶标中,这为进一步进行体内应用提供了有希望的证据。