Cancer remains one of the most pressing global health challenges, driving the need for innovative treatment strategies. Boron neutron capture therapy (BNCT) offers a highly selective approach to destroying cancer cells while sparing healthy tissues. To improve boron delivery, Fe(3)O(4)@Au nanoparticles were developed and functionalized with a boron-containing carborane compound. Fe(3)O(4) nanoparticles were synthesized and covered by gold, followed by (3-Aminopropyl)triethoxysilane (APTES) modification to introduce amino groups for carborane immobilization. Comprehensive characterization using SEM, DLS, FTIR, EDX, Brunauer-Emmett-Teller (BET), and XRD confirmed successful functionalization at each stage. TEM confirmed the final structure and elemental composition of the nanoparticles. BET analysis revealed a surface area of 94.69 m(2)/g and a pore volume of 0.51 cm(3)/g after carborane loading. Initial release studies in PBS demonstrated the removal of only loosely bound carborane within 48 h, with FTIR confirming stable retention of the compound on the nanoparticle surface. The modified nanoparticles achieved a stable zeta potential of -20 mV. The particles showed low toxicity within a range of concentrations (0-300 μg Fe/mL) and were efficiently accumulated by U251MG cells. These results demonstrate the potential of the obtained nanoparticles to carry boron and gold for their possible application as a theranostic agent.
Carborane-Containing Iron Oxide@Gold Nanoparticles for Potential Application in Neutron Capture Therapy.
含碳硼烷的氧化铁@金纳米粒子在中子俘获疗法中的潜在应用
阅读:13
作者:Bekbol Zhangali A, Izbasar Kairat A, Zaboronok Alexander, Lissovskaya Lana I, Yang Haolan, Pihosh Yuriy, Ishikawa Eiichi, Shakirzyanov Rafael I, Korolkov Ilya V
| 期刊: | Nanomaterials | 影响因子: | 4.300 |
| 时间: | 2025 | 起止号: | 2025 Aug 13; 15(16):1243 |
| doi: | 10.3390/nano15161243 | ||
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。
