前药
乙二醇
化学
紫杉醇
组合化学
细胞毒性
娴熟的
药品
药理学
有机化学
生物化学
体外
癌症
医学
内科学
作者
Yaqi Li,Yixin Sun,Qing Wang,Shuo Wang,Cui-Yun Liu,Yuetong Huang,Wenxin Zhong,Xiyan Wang,Wenjing Wang,Shiyi Zuo,Xianbao Shi,Xiaohui Pu,Jin Sun,Zhonggui He,Bingjun Sun
出处
期刊:ACS central science
[American Chemical Society]
日期:2024-11-20
卷期号:10 (12): 2253-2265
被引量:7
标识
DOI:10.1021/acscentsci.4c01004
摘要
Prodrug-based nanoassemblies are promising platforms for cancer therapy. Prodrugs typically consist of three main components: drug modules, intelligent response modules, and modification modules. However, the available modification modules are usually hydrophobic aliphatic side chains, which affect the activation efficiency of the prodrugs. Herein, hydrophilic ethylene glycol fragments were inserted between the modification modules and the response modules, and the important effects of hydrophilic fragments on the assembly, drug release, and therapeutic index of the prodrugs were investigated. Notably, the introduction of hydrophilic fragments affected the intermolecular forces of the prodrugs and increased the interaction of hydrogen bonding. In addition, hydrophilic fragments significantly improved the redox drug release profiles, which affected the therapeutic index of the prodrug nanoassemblies. PTX-SS-OA NPs with hydrophilic fragments exhibited increased redox sensitivity, enhanced cytotoxicity, and superior antitumor efficacy. In comparison, PTX-SS-OAL NPs without hydrophilic fragments showed limited redox sensitivity and cytotoxicity but displayed better safety. Overall, the hydrophilic fragment is a critical determinant in modulating the therapeutic index of the prodrug nanoassemblies, which contributes to the development of advanced prodrug nanodelivery systems.
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