纳米医学
PEG比率
药品
药物输送
药理学
材料科学
靶向给药
纳米技术
癌细胞
癌症
癌症研究
纳米颗粒
医学
内科学
财务
经济
作者
Yang Li,Jinyan Lin,Yu Huang,Yanxiu Li,Xiangrui Yang,Hongjie Wu,Shichao Wu,Liya Xie,Lizong Dai,Zhenqing Hou
标识
DOI:10.1021/acsami.5b07348
摘要
We constructed 10-hydroxycamptothecin (CPT) "nanodrugs" with functionalization of lipid-PEG-methotrexate (MTX) to prepare high-drug-loaded, and sustained/controlled-release MTX-PEG-CPT nanorods (NRs), in which MTX drug itself can serve as a specific "targeting ligand". The self-targeted nanodrug can codeliver both CPT and MTX drugs with distinct anticancer mechanisms. Furthermore, MTX-PEG-CPT NRs significantly reduced burst release, improved blood circulation and tumor accumulation, enhanced cellular uptake, and synergistically increased anticancer effect against tumor cells compared with MTX-PEG-CPT nanospheres (NSs) and either both free drugs or individual free drug. Therefore, the synergistic targeting/therapeuticy nano-multi-drug codelivery assisted by shape design may advantageously offer a promising new strategy for nanomedicine.
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