介孔二氧化硅
螯合作用
生物相容性
纳米颗粒
纳米技术
化学
材料科学
神经毒性
生物物理学
介孔材料
生物化学
毒性
有机化学
生物
催化作用
作者
Jie Geng,Meng Li,Li Wu,Cuie Chen,Xiaogang Qu
标识
DOI:10.1002/adhm.201200067
摘要
Abstract Metal ions play important roles in amyloid aggregation and neurotoxicity. Metal‐ion chelation therapy has been used in clinical trials for Alzheimer's disease (AD) treatment. However, clinical trial studies have shown that long‐term use of metal chelator can cause adverse side effect, subacute myelo‐optic neuropathy. Nanoparticle engineering processes have become promising approaches for efficiently drugs delivery. A series of modified mesoporous silica nanoparticles (MSNs) using redox, pH, competitive binding, light, and enzyme as actuators have been demonstrated. Recently, significant advances in sensing oxidative stress have been made by taking advantage of specific chemistry between cellular oxidants such as H 2 O 2 . Here we report a biocompatible delivery platform by using H 2 O 2 responsive controlled‐release system to realize target delivery of AD therapeutic metal chelator. The advantage of this novel strategy is that metal chelator can only be released by the increased levels of H 2 O 2 , thus, it would not interfere with the healthy metal homeostasis and can overcome strong side effect of metal chelator after long‐term use. By taking advantage of the good biocompatibility, cellular uptake properties, and efficient intracellular release of metal chelators, the delivery system is promising for future in vivo controlled‐release biomedical applications.
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