CAS Key Laboratory of Design and Assembly of Functional Nanostructures, and Fujian Provincial Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter , Chinese Academy of Sciences , Fuzhou 350002 , China.
Department of Translational Medicine, Xiamen Institute of Rare Earth Materials , Chinese Academy of Sciences , Xiamen 361024 , P. R. China.
Mol Pharm. 2019 May 6;16(5):1982-1998. doi: 10.1021/acs.molpharmaceut.8b01335. Epub 2019 Apr 3.
Locating nanomedicines at the active sites plays a pivotal role in the nanoparticle-based cancer therapy field. Herein, a multifunctional nanotherapeutic is designed by using graphene oxide (GO) nanosheets with rich carboxyl groups as the supporter for hyaluronic acid (HA)-methotrexate (MTX) prodrug modification via an adipicdihydrazide cross-linker, achieving synergistic multistage tumor-targeting and combined chemo-photothermal therapy. As a tumor-targeting biomaterial, HA can increase affinity of the nanocarrier toward CD44 receptor for enhanced cellular uptake. MTX, a chemotherapeutic agent, can also serve as a tumor-targeting enhancer toward folate receptor based on its similar structure with folic acid. The prepared nanosystems possess a sheet shape with a dynamic size of approximately 200 nm and pH-responsive drug release. Unexpectedly, the physiological stability of HA-MTX prodrug-decorated GO nanosystems in PBS, serum, and even plasma is more excellent than that of HA-decorated GO nanosystems, while both of them exhibit an enhanced photothermal effect than GO nanosheets. More importantly, because of good blood compatibility as well as reduced undesired interactions with blood components, HA-MTX prodrug-decorated GO nanosystems exhibited remarkably superior accumulation at the tumor sites by passive and active targeting mechanisms, achieving highly effective synergistic chemo-photothermal therapeutic effect upon near-infrared laser irradiation, efficient ablation of tumors, and negligible systemic toxicity. Hence, the HA-MTX prodrug-decorated hybrid nanosystems have a promising potential for synergistic multistage tumor-targeting therapy.
将纳米药物定位在活性部位在基于纳米粒子的癌症治疗领域中起着至关重要的作用。在此,通过使用具有丰富羧基的氧化石墨烯 (GO) 纳米片作为载体,通过己二酰二肼交联剂对透明质酸 (HA)-甲氨蝶呤 (MTX) 前药进行修饰,设计了一种多功能纳米治疗剂,实现了协同的多阶段肿瘤靶向和联合化疗-光热治疗。作为一种肿瘤靶向生物材料,HA 可以增加纳米载体对 CD44 受体的亲和力,从而增强细胞摄取。MTX 作为一种化疗药物,也可以作为叶酸受体的肿瘤靶向增强剂,因为它的结构与叶酸相似。所制备的纳米系统具有约 200nm 的动态尺寸的片状形状和 pH 响应性药物释放。出乎意料的是,HA-MTX 前药修饰的 GO 纳米系统在 PBS、血清甚至血浆中的生理稳定性比 HA 修饰的 GO 纳米系统更优异,而它们在光热效应方面均优于 GO 纳米片。更重要的是,由于良好的血液相容性以及与血液成分的减少的非预期相互作用,HA-MTX 前药修饰的 GO 纳米系统通过被动和主动靶向机制在肿瘤部位具有显著的蓄积作用,在近红外激光照射下实现了高效的协同化疗-光热治疗效果,高效消融肿瘤,并且系统毒性可以忽略不计。因此,HA-MTX 前药修饰的杂化纳米系统具有协同多阶段肿瘤靶向治疗的巨大潜力。