连接器
结合
阿霉素
纳米颗粒
化学
药物输送
纳米医学
癌细胞
药理学
生物物理学
靶向给药
癌症
纳米技术
药品
细胞毒性
喜树碱
体内
癌症研究
生物化学
体外
材料科学
化疗
医学
生物
外科
生物技术
有机化学
内科学
数学分析
计算机科学
数学
操作系统
作者
Rong Xu,Guodong Zhang,Junhua Mai,Xiaoyong Deng,Víctor Segura-Ibarra,Suhong Wu,Jianliang Shen,Haoran Liu,Zhenhua Hu,Lingxiao Chen,Yi Huang,Eugene J. Koay,Yu Huang,Jun Liu,Joe Ensor,Elvin Blanco,Xuewu Liu,Mauro Ferrari,Haifa Shen
摘要
The efficacy of cancer drugs is often limited because only a small fraction of the administered dose accumulates in tumors. Here we report an injectable nanoparticle generator (iNPG) that overcomes multiple biological barriers to cancer drug delivery. The iNPG is a discoidal micrometer-sized particle that can be loaded with chemotherapeutics. We conjugate doxorubicin to poly(L-glutamic acid) by means of a pH-sensitive cleavable linker, and load the polymeric drug (pDox) into iNPG to assemble iNPG-pDox. Once released from iNPG, pDox spontaneously forms nanometer-sized particles in aqueous solution. Intravenously injected iNPG-pDox accumulates at tumors due to natural tropism and enhanced vascular dynamics and releases pDox nanoparticles that are internalized by tumor cells. Intracellularly, pDox nanoparticles are transported to the perinuclear region and cleaved into Dox, thereby avoiding excretion by drug efflux pumps. Compared to its individual components or current therapeutic formulations, iNPG-pDox shows enhanced efficacy in MDA-MB-231 and 4T1 mouse models of metastatic breast cancer, including functional cures in 40-50% of treated mice.
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