Kim Junghyun, Jay Michael
Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC 27599, USA.
Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC 27599, USA.
Nucl Med Biol. 2017 Sep;52:42-48. doi: 10.1016/j.nucmedbio.2017.05.009. Epub 2017 Jun 1.
Neutron-activation is a promising method of generating radiotherapeutics with minimal handling of radioactive materials. Graphene oxide nanoplatelets (GONs) were examined as a carrier for neutron-activatable holmium with the purpose of exploiting inherent characteristics for theranostic application. GONs were hypothesized to be an ideal candidate for this application owing to their desirable characteristics such as a rigid structure, high metal loading capacity, low density, heat resistance, and the ability to withstand harsh environments associated with the neutron-activation process. Non-covalently PEGylated GONs (GONs-PEG) offered enhanced dispersibility and biocompatibility, and also exhibited increased holmium loading capacity nearly two-fold greater than GONs. Holmium leaching was investigated over a wide pH range, including conditions that mimic the tumor microenvironment, following neutron irradiation. The in vitro cell-based cytotoxicity analysis of GONs-based formulations with non-radioactive holmium confirmed their safety profile within cells. The results demonstrate the potential of GONs as a carrier of neutron-activatable radiotherapeutic agents.
中子活化是一种很有前景的方法,可在对放射性材料进行最少处理的情况下生成放射治疗药物。氧化石墨烯纳米片(GONs)被作为可中子活化钬的载体进行研究,目的是利用其固有特性用于诊疗应用。由于GONs具有诸如刚性结构、高金属负载能力、低密度、耐热性以及能够承受与中子活化过程相关的恶劣环境等理想特性,因此被假定为该应用的理想候选者。非共价聚乙二醇化的GONs(GONs-PEG)具有增强的分散性和生物相容性,并且钬负载能力也有所提高,几乎比GONs高出两倍。在中子辐照后,研究了在包括模拟肿瘤微环境条件在内的较宽pH范围内的钬浸出情况。对含有非放射性钬的基于GONs的制剂进行的体外细胞毒性分析证实了它们在细胞内的安全性。结果证明了GONs作为可中子活化放射治疗剂载体的潜力。