Aptamer-based self-assembled nanomicelle enables efficient and targeted drug delivery

被引:6
|
作者
Chen, Ganghui [1 ,2 ]
Mao, Dongsheng [1 ]
Wang, Xuan [1 ]
Chen, Jingqi [1 ]
Gu, Chao [1 ]
Huang, Shuqin [2 ]
Yang, Yu [1 ]
Zhang, Fang [2 ]
Tan, Weihong [1 ]
机构
[1] Shanghai Jiao Tong Univ, Inst Mol Med IMM, Sch Med, Renji Hosp,Coll Chem & Chem Engn, Shanghai 200240, Peoples R China
[2] Fuzhou Univ, Coll Biol Sci & Engn, Fuzhou 350108, Peoples R China
基金
中国国家自然科学基金;
关键词
Aptamer micelles; Self-assembly; Specific cell recognition; DNA; NANOMATERIALS; APOPTOSIS; MICELLES; CELLS;
D O I
10.1186/s12951-023-02164-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nucleic acid aptamer-based nanomicelles have great potential for nanomedicine and nanotechnology applications. However, amphiphilic aptamer micelles are known to be inherently unstable upon interaction with cell membranes in the physiological environment, thus potentially compromising their specific targeting against cancer cells. This flaw is addressed in the present work which reports a superstable micellar nanodelivery system as an amphiphilic copolymer self-assembled micelle composed of nucleic acid aptamer and polyvalent hydrophobic poly(maleic anhydride-alt-1-octadecene) (C18PMH). Using Ce6 as a drug model, these C18-aptamer micelles exhibit efficient tumor-targeting and -binding ability, facilitating the entry of Ce6 into targeted cells for photodynamic therapy. In addition, they can be loaded with other hydrophobic drugs and still demonstrate favorable therapeutic effects. As such, these C18-aptamer micelles can serve as a universal platform for loading multiple drugs, providing a safer and more effective solution for treating cancer.
引用
收藏
页数:12
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