体内
药品
活性氧
量子点
发病机制
炎症
血脑屏障
药理学
材料科学
癌症研究
化学
纳米技术
医学
免疫学
生物化学
生物
中枢神经系统
内科学
生物技术
作者
Xiating Qi,Lianxin Li,Pengkun Ye,Meng Xie
标识
DOI:10.1002/adhm.202303211
摘要
Abstract The complex pathological mechanism of Alzheimer's disease (AD) limits the efficacy of simple drug therapy, and drugs are difficult to penetrate the blood‐brain barrier (BBB). Therefore, it is a breakthrough to enhance the therapeutic effect of AD by rationally using multiple therapeutic strategies to inhibit multiple pathological targets. In this study, macrophage membrane (MM) with active targeting inflammation function is used to functionalize molybdenum disulfide quantum dots (MoS 2 QDs) with the properties of elimination of reactive oxygen species (ROS) and anti‐A β 1‐42 deposition to form the nano drug (MoS 2 QDs/MM), and play the role of multi‐target combined therapy with NIR. The results show that MoS 2 QDs/MM has a targeted therapeutic effect on ROS elimination and anti‐deposition of A β 1‐42 . In addition, the combined therapy group effectively reduced A β 1‐42 mediated cytotoxicity. The modification of MM could effectively target the brain, and NIR irradiation could actively increase the cross of BBB of materials. In vivo behavioral study also show that APP/PS1 mice in the combined treatment group showed the similar exploration desire and learning ability to mice in the group of WT. MoS 2 QDs/MM is an excellent nano drug with multiple effects, which has advantages in the field of neurological diseases with crisscross pathogenesis.
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