纳米载体
癌细胞
介孔有机硅
纳米颗粒
谷胱甘肽
细胞内
化学
细胞毒性
生物物理学
药物输送
介孔二氧化硅
介孔材料
材料科学
纳米技术
癌症
生物化学
酶
催化作用
体外
内科学
生物
医学
作者
Yannan Yang,Jingjing Wan,Yuting Niu,Zhengying Gu,Jun Zhang,Meihua Yu,Chengzhong Yu
标识
DOI:10.1021/acs.chemmater.6b03896
摘要
The design of smart nanocarriers that could recognize and differentiate cancer cells and normal cells is of great importance in drug delivery. Here we report the first example of cancer cell-specific degradable dendritic mesoporous organosilica nanoparticles (DDMONs). A unique pore structure-dependent glutathione (GSH)-responsive degradation behavior is revealed: the degradation rates of two nanoparticles with different pore sizes are similar in normal cells ("leveling effect"), while large-pore DDMONs show a faster degradation rate than small-pore nanoparticles in cancer cells with relatively high intracellular GSH levels ("differentiating effect"). The cancer cell-specific degradability and concomitant cargo release lead to efficient protein delivery toward cancer cells but reduced cytotoxicity toward normal cells.
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