纳米载体
生物降解
介孔二氧化硅
药物输送
分散性
盐酸阿霉素
体内
材料科学
靶向给药
纳米颗粒
纳米技术
聚乙二醇
PEG比率
核化学
阿霉素
化学工程
化学
介孔材料
医学
有机化学
高分子化学
化疗
生物
外科
经济
催化作用
财务
工程类
生物技术
作者
Mo Cheng,Yan Yu,Wending Huang,Meng Fang,Yong Chen,Chunmeng Wang,Weiluo Cai,Shuyu Zhang,Wenxing Wang,Wangjun Yan
标识
DOI:10.1021/acsbiomaterials.0c00507
摘要
The development of new nanocarriers with desired degradability and targeted ability is of great significance for efficient drug delivery. In this work, a monodisperse hollow structured MnO2 (H-MnO2) with a mesoporous shell is prepared and functionalized for efficient targeted drug delivery. The highly monodisperse H-MnO2 with a uniform morphology was obtained by in situ growing MnO2 on solid silica nanoparticles and subsequently removing the silica core. Then, the H-MnO2 is successively modified with polyethylene glycol and targeted molecule folate (FA). The resultant H-MnO2-FA shows excellent colloidal stability and high drug-loading content (∼58.2%) of the antitumor drug doxorubicin hydrochloride (DOX). The H-MnO2-FA possesses acid-responsive T1-weighted magnetic resonance imaging ability. The pH-dependent biodegradation behavior of H-MnO2-FA is directly observed in vitro and confirmed by in vivo imaging, which is expected to favor the potential clearance of this hollow structured nanocarrier and eliminate its long-term toxicity. In addition, the DOX-loaded H-MnO2-FA also demonstrates excellent cancer cell-killing effect and tumor inhibition efficacy.
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