多重耐药
级联
药品
纳米颗粒
材料科学
抗药性
纳米技术
癌症研究
药理学
化学
生物
微生物学
色谱法
作者
Mingzhou Ye,Yuxin Han,Jianbin Tang,Ying Piao,Xiangrui Liu,Zhuxian Zhou,Jianqing Gao,Jianghong Rao,Youqing Shen
标识
DOI:10.1002/adma.201702342
摘要
A cascade amplification release nanoparticle (CARN) is constructed by the coencapsulation of β-lapachone and a reactive-oxygen-species (ROS)-responsive doxorubicin (DOX) prodrug, BDOX, in polymeric nanoparticles. Releasing β-lapachone first from the CARNs selectively increases the ROS level in cancer cells via NAD(P)H:quinone oxidoreductase-1 (NQO1) catalysis, which induces the cascade amplification release of DOX and overcomes multidrug resistance (MDR) in cancer cells, producing a remarkably improved therapeutic efficacy against MDR tumors with minimal side effects.
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