College of Science, Northwest A&F University, Yangling, Shaanxi 712100 (P.R. China).
Angew Chem Int Ed Engl. 2014 Nov 24;53(48):13126-30. doi: 10.1002/anie.201407272. Epub 2014 Sep 29.
A novel ferrocenium capped amphiphilic pillar[5]arene (FCAP) was synthesized and self-assembled to cationic vesicles in aqueous solution. The cationic vesicles, displaying low cytotoxicity and significant redox-responsive behavior due to the redox equilibrium between ferrocenium cations and ferrocenyl groups, allow building an ideal glutathione (GSH)-responsive drug/siRNA co-delivery system for rapid drug release and gene transfection in cancer cells in which higher GSH concentration exists. This is the first report of redox-responsive vesicles assembled from pillararenes for drug/siRNA co-delivery; besides enhancing the bioavailability of drugs for cancer cells and reducing the adverse side effects for normal cells, these systems can also overcome the drug resistance of cancer cells. This work presents a good example of rational design for an effective stimuli-responsive drug/siRNA co-delivery system.
一种新型的二茂铁鎓封端的两亲性柱[5]芳烃(FCAP)被合成,并在水溶液中自组装成阳离子囊泡。由于二茂铁阳离子和二茂铁基之间的氧化还原平衡,这些阳离子囊泡表现出低细胞毒性和显著的氧化还原响应行为,允许构建一个理想的谷胱甘肽(GSH)响应型药物/ siRNA 共递药系统,用于在存在更高 GSH 浓度的癌细胞中快速释放药物和基因转染。这是首次报道从柱芳烃组装的氧化还原响应性囊泡用于药物/ siRNA 共递药;除了提高药物对癌细胞的生物利用度并减少对正常细胞的不良副作用外,这些系统还可以克服癌细胞的耐药性。这项工作为有效刺激响应型药物/ siRNA 共递药系统的合理设计提供了一个很好的范例。