Mhanna Karim, Qian Wei, Zhong Ziyun, Brooks Allen F, Ouchi Erika, Stauff Jenelle, Arteaga Janna, Papachristou Maria, Datseris Ioannis E, Liu Bing, Shao Xia, Scott Peter J H
Department of Radiology, University of Michigan, Ann Arbor, MI 48109, USA.
IMRA America Inc., Ann Arbor, MI 48105, USA.
Pharmaceuticals (Basel). 2023 Jan 2;16(1):71. doi: 10.3390/ph16010071.
Gold nanoparticles (AuNPs) are cutting-edge platforms for combined diagnostic and therapeutic approaches due to their exquisite physicochemical and optical properties. Using the AuNPs physically produced by femtosecond pulsed laser ablation of bulk Au in deionized water, with a capping agent-free surface, the conjugation of functional ligands onto the AuNPs can be tunable between 0% and 100% coverage. By taking advantage of this property, AuNPs functionalized by two different types of active targeting ligands with predetermined ratios were fabricated. The quantitatively controllable conjugation to construct a mixed monolayer of multiple biological molecules at a certain ratio onto the surface of AuNPs was achieved and a chelator-free Cu-labeling method was developed. We report here the manufacture, radiosynthesis and bioevaluation of three different types of dual-ligand AuNPs functionalized with two distinct ligands selected from glucose, arginine-glycine-aspartate (RGD) peptide, and methotrexate (MTX) for tumor theragnosis. The preclinical evaluation demonstrated that tumor uptakes and retention of two components AuNP conjugates were higher than that of single-component AuNP conjugates. Notably, the glucose/MT- modified dual-ligand AuNP conjugates showed significant improvement in tumor uptake and retention. The novel nanoconjugates prepared in this study make it possible to integrate several modalities with a single AuNP for multimodality imaging and therapy, combining the power of chemo-, thermal- and radiation therapies together.
由于其优异的物理化学和光学性质,金纳米颗粒(AuNPs)是用于联合诊断和治疗方法的前沿平台。使用飞秒脉冲激光烧蚀去离子水中的块状金物理产生的、表面无封端剂的AuNPs,功能配体在AuNPs上的共轭覆盖率可在0%至100%之间调节。利用这一特性,制备了由两种不同类型的具有预定比例的活性靶向配体功能化的AuNPs。实现了以一定比例在AuNPs表面定量可控地共轭构建多种生物分子的混合单层,并开发了一种无螯合剂的铜标记方法。我们在此报告了三种不同类型的双配体AuNPs的制造、放射性合成和生物评估,这些AuNPs用从葡萄糖、精氨酸 - 甘氨酸 - 天冬氨酸(RGD)肽和甲氨蝶呤(MTX)中选出的两种不同配体进行功能化,用于肿瘤诊疗。临床前评估表明,双组分AuNP共轭物的肿瘤摄取和滞留高于单组分AuNP共轭物。值得注意的是,葡萄糖/MT修饰的双配体AuNP共轭物在肿瘤摄取和滞留方面有显著改善。本研究中制备的新型纳米共轭物使得将多种模式整合到单个AuNP上以进行多模态成像和治疗成为可能,将化学、热和放射治疗的力量结合在一起。