氧化应激
二甲双胍
谷胱甘肽
药理学
脊髓损伤
炎症
细胞凋亡
体内
药物输送
医学
化学
脊髓
生物化学
免疫学
内分泌学
生物
糖尿病
酶
生物技术
精神科
有机化学
作者
Yu Qi,Xue Jiang,Xiaoyao Liu,Wenwen Shen,Xifan Mei,He Tian,Chao Wu
出处
期刊:Biomaterials advances
日期:2022-01-18
卷期号:133: 112668-112668
被引量:23
标识
DOI:10.1016/j.msec.2022.112668
摘要
Spinal cord injury (SCI) causes a range of pathological responses, including oxidative stress, inflammation and apoptosis. In SCI treatment, whether an effective drug preparation can cross the blood-spinal cord barrier (BSCB) to the injury site is closely related to its therapeutic effect. Metformin (Met) is a glucose-lowering drug that shows a good effect for the treatment of SCI. However, it cannot cross the BSCB, which limits its application. In this study, we prepared glutathione-modified macrophage-derived cell membranes encapsulating metformin nanogels (Met-CNG-GSH) to solve this problem. Drug release and pharmacokinetics study results indicated that Met-CNG-GSH exhibits a slow release effect, and in vivo imaging demonstrated that Met-CNG-GSHs accumulated at the injury site, indicating that it has a good targeting effect. Animal experiments demonstrated that Met-CNG-GSH has a good therapeutic effect in alleviating oxidative stress, inflammation, and apoptosis. Therefore, Met-CNG-GSH represents a potential treatment for SCI.
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