Xu Mingyu, Zhou Yifan, Xu Yufeng, Shao An, Han Haijie, Ye Juan
Eye Center, The Second Affiliated Hospital, School of Medicine, Zhejiang Provincial Key Laboratory of Ophthalmology, Zhejiang Provincial Clinical Research Center for Eye Diseases, Zhejiang Provincial Engineering Institute on Eye Diseases, Zhejiang University, 88 Jiefang Road, Hangzhou, 310009, China.
Adv Sci (Weinh). 2025 Mar;12(9):e2408436. doi: 10.1002/advs.202408436. Epub 2025 Jan 10.
Age-related macular degeneration (AMD), characterized by choroidal neovascularization (CNV), is the global leading cause of irreversible blindness. Current first-line therapeutics, vascular endothelial growth factor (VEGF) antagonists, often yield incomplete and suboptimal vision improvement, necessitating the exploration of novel and efficacious therapeutic approaches. Herein, a supramolecular engineering strategy to construct moringin (MOR) loaded α-cyclodextrin (α-CD) coated nanoceria (M@CCNP) is constructed, where the hydroxy and newly formed carbonyl groups of α-CD interact with the nanoceria surface via O─Ce conjunction and the isothiocyanate group of MOR inserts deeply into the α-CD cavity via host-guest interaction. By exploiting the recycling reactive oxygen species (ROS) scavenging capability of nanoceria and the anti-inflammation properties of MOR, the two-level strike during AMD pathogenesis can be precisely blocked by M@CCNP. Remarkably, excellent therapeutic efficacy to CNV is observed in vivo, achieving over 80% reduction in neovascularization and over 60% reduction in leakage area. In summary, the supramolecular engineered nanoceria provides an efficient approach for amelioration of AMD by blocking the two-level strike, and presents significant potential as an exceptional drug delivery platform, particularly for ROS-related diseases.
年龄相关性黄斑变性(AMD)以脉络膜新生血管形成(CNV)为特征,是全球不可逆失明的主要原因。目前的一线治疗药物,即血管内皮生长因子(VEGF)拮抗剂,往往只能带来不完全且不理想的视力改善,因此有必要探索新的有效治疗方法。在此,构建了一种超分子工程策略,以制备负载有辣木素(MOR)的α-环糊精(α-CD)包被的纳米氧化铈(M@CCNP),其中α-CD的羟基和新形成的羰基通过O─Ce键与纳米氧化铈表面相互作用,而MOR的异硫氰酸酯基团通过主客体相互作用深入插入α-CD腔中。通过利用纳米氧化铈的循环活性氧(ROS)清除能力和MOR的抗炎特性,M@CCNP可以精确阻断AMD发病机制中的两级攻击。值得注意的是,在体内观察到M@CCNP对CNV具有优异的治疗效果,新生血管形成减少超过80%,渗漏面积减少超过60%。总之,超分子工程化的纳米氧化铈通过阻断两级攻击为改善AMD提供了一种有效方法,并作为一种特殊的药物递送平台展现出巨大潜力,特别是对于与ROS相关的疾病。