超分子化学
胶束
聚乙二醇
环糊精
喜树碱
材料科学
氧化还原
体内
生物相容性
组合化学
药物输送
生物物理学
化学
纳米技术
有机化学
水溶液
晶体结构
生物技术
生物
作者
Yang Kang,Xin Jü,Li‐Sheng Ding,Sheng Zhang,Bang‐Jing Li
标识
DOI:10.1021/acsami.6b14640
摘要
A dual redox and biorelevant triggered supramolecular system is developed through noncovalent supramolecular inclusion interactions between the ferrocene (Fc) modified on camptothecin (CPT) and β-cyclodextrin (β-CD) at the end of methoxy polyethylene glycol (mPEG). With these two segments, a stable noncovalent supramolecular structure, i.e., mPEG-β-CD/Fc-CPT, can be formed, and then self-assembled into micellar structures in water. Interestingly, these supramolecular micelles showed uniform sphere structure, high and constant drug loading content, hyper-fast redox-responsive drug release, and exhibited equal cellular proliferation inhibition toward A549 cancer cells. The cytotoxicity evaluation of mPEG-β-CD also indicated good biocompatibility. In vivo results revealed the mPEG-β-CD/Fc-CPT nanoparticles had higher in vivo efficacy without side effects. It is anticipated this supramolecular complex may serve as a new kind of promising alternative for drug delivery systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI