Zhao Dongju, Tang Yuqing, Suo Xinjun, Zhang Chaonan, Dou Yan, Chang Jin
School of Life Sciences, Tianjin University, Tianjin 300072, China.
Department of Radiology and Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital, Tianjin 300052, China.
Innovation (Camb). 2021 Sep 1;2(4):100160. doi: 10.1016/j.xinn.2021.100160. eCollection 2021 Nov 28.
Antioxidation and adjustable treatment strategies are critical for the effective treatment of Alzheimer's disease (AD). Here, we design a dual-targeted Prussian blue nanoformulation (PTCN) that can cross the blood-brain barrier and target amyloid beta aggregates further exert antioxidant effects. An adjustable gradient dosing strategy with PTCN is used for the first time to design the preventive and therapeutic trials based on the severity of oxidative stress at different AD stages. The results show that PTCN could effectively ameliorate AD-related pathological processes, improve the cognitive decline, and rescue hippocampal atrophy of APP/PS1 mice in both preventive and therapeutic trials. Altogether, PTCN provided here is a successful combination of three traditional biomaterials with good biosafety, which has broad prospects for the early prevention, mild remission, and late treatment of AD, and is expected to be developed into personalized therapeutic drugs and healthcare products for clinical AD in the future.
抗氧化和可调节的治疗策略对于阿尔茨海默病(AD)的有效治疗至关重要。在此,我们设计了一种双靶向普鲁士蓝纳米制剂(PTCN),其能够穿过血脑屏障并靶向淀粉样β聚集体,进而发挥抗氧化作用。首次采用PTCN的可调节梯度给药策略,根据不同AD阶段氧化应激的严重程度设计预防和治疗试验。结果表明,在预防和治疗试验中,PTCN均可有效改善AD相关病理过程,改善认知功能下降,并挽救APP/PS1小鼠的海马萎缩。总之,本文提供的PTCN是三种传统生物材料的成功组合,具有良好的生物安全性,在AD的早期预防、轻度缓解和晚期治疗方面具有广阔前景,有望在未来开发成为针对临床AD的个性化治疗药物和保健产品。