Zavestovskaya Irina N, Popov Anton L, Kolmanovich Danil D, Tikhonowski Gleb V, Pastukhov Andrei I, Savinov Maxim S, Shakhov Pavel V, Babkova Julia S, Popov Anton A, Zelepukin Ivan V, Grigoryeva Maria S, Shemyakov Alexander E, Klimentov Sergey M, Ryabov Vladimir A, Prasad Paras N, Deyev Sergey M, Kabashin Andrei V
P. N. Lebedev Physical Institute of the Russian Academy of Sciences, Leninsky Prospect 53, 119991 Moscow, Russia.
Bionanophotonics Laboratory, Institute of Engineering Physics for Biomedicine (PhysBio), National Research Nuclear University MEPhI (Moscow Engineering Physics Institute), Kashirskoe Shosse 31, 115409 Moscow, Russia.
Nanomaterials (Basel). 2023 Jul 26;13(15):2167. doi: 10.3390/nano13152167.
Proton therapy is one of the promising radiotherapy modalities for the treatment of deep-seated and unresectable tumors, and its efficiency can further be enhanced by using boron-containing substances. Here, we explore the use of elemental boron (B) nanoparticles (NPs) as sensitizers for proton therapy enhancement. Prepared by methods of pulsed laser ablation in water, the used B NPs had a mean size of 50 nm, while a subsequent functionalization of the NPs by polyethylene glycol improved their colloidal stability in buffers. Laser-synthesized B NPs were efficiently absorbed by MNNG/Hos human osteosarcoma cells and did not demonstrate any remarkable toxicity effects up to concentrations of 100 ppm, as followed from the results of the MTT and clonogenic assay tests. Then, we assessed the efficiency of B NPs as sensitizers of cancer cell death under irradiation by a 160.5 MeV proton beam. The irradiation of MNNG/Hos cells at a dose of 3 Gy in the presence of 80 and 100 ppm of B NPs led to a 2- and 2.7-fold decrease in the number of formed cell colonies compared to control samples irradiated in the absence of NPs. The obtained data unambiguously evidenced the effect of a strong proton therapy enhancement mediated by B NPs. We also found that the proton beam irradiation of B NPs leads to the generation of reactive oxygen species (ROS), which evidences a possible involvement of the non-nuclear mechanism of cancer cell death related to oxidative stress. Offering a series of advantages, including a passive targeting option and the possibility of additional theranostic functionalities based on the intrinsic properties of B NPs (e.g., photothermal therapy or neutron boron capture therapy), the proposed concept promises a major advancement in proton beam-based cancer treatment.
质子治疗是治疗深部和不可切除肿瘤的一种有前景的放射治疗方式,通过使用含硼物质可进一步提高其疗效。在此,我们探索使用元素硼(B)纳米颗粒(NPs)作为质子治疗增强的敏化剂。通过水中脉冲激光烧蚀法制备的所用B NPs平均尺寸为50 nm,而随后用聚乙二醇对NPs进行功能化改善了它们在缓冲液中的胶体稳定性。激光合成的B NPs能被MNNG/Hos人骨肉瘤细胞有效吸收,并且根据MTT和克隆形成试验测试结果,在浓度高达100 ppm时未显示出任何显著的毒性作用。然后,我们评估了B NPs作为160.5 MeV质子束照射下癌细胞死亡敏化剂的效率。与在无NPs情况下照射的对照样品相比,在存在80和100 ppm B NPs的情况下以3 Gy剂量照射MNNG/Hos细胞导致形成的细胞集落数量分别减少了2倍和2.7倍。所获得的数据明确证明了B NPs介导的强烈质子治疗增强效果。我们还发现质子束照射B NPs会导致活性氧(ROS)的产生,这证明了与氧化应激相关的癌细胞死亡非核机制可能参与其中。所提出的概念具有一系列优势,包括被动靶向选项以及基于B NPs固有特性(例如光热疗法或中子硼俘获疗法)实现额外治疗诊断功能的可能性,有望在基于质子束的癌症治疗方面取得重大进展。