前药
紫杉醇
纳米纤维
两亲性
化学
二硫键
细胞毒性
药品
组合化学
纳米技术
材料科学
化疗
体外
药理学
共聚物
有机化学
生物化学
医学
外科
聚合物
作者
Shaojin Lu,Dengyuan Hao,Xiujuan Xiang,Qing Pei,Zhigang Xie
标识
DOI:10.1016/j.jconrel.2023.02.013
摘要
The facile availability of nanoformulations with enhanced antitumor performance remains a big challenge. Herein, we synthesize paclitaxel prodrugs with amphiphilic structures and robust assembling ability. Carboxylated paclitaxel prodrugs (PSCB) containing disulfide bonds prefer to form exquisite nanofibers, while phenylcarbinol end capped paclitaxel prodrugs (PSP) assemble into spherical nanoparticles. The transformation of morphology from nanofibers to nanorods can be realized via tuning the content of paclitaxel. Hydrophilic domains of PSCB nanofibers accelerate the cleavage of disulfide bond for rapid drug release in tumor cells, thus exhibiting the enhanced cytotoxicity and antitumor activity. This study provides a crucial insight into the functional design of hydrophobic drugs to improve chemotherapy.
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