Autocatalytic Morphology Transformation Platform for Targeted Drug Accumulation

被引:147
作者
Cheng, Dong-Bing [1 ]
Wang, Dong [1 ]
Gao, Yu-Juan [1 ]
Wang, Lei [1 ]
Qiao, Zeng-Ying [1 ]
Wang, Hao [1 ]
机构
[1] Univ Chinese Acad Sci, Natl Ctr Nanosci & Technol NCNST, CAS Key Lab Biomed Effects Nanomat & Nanosafety, CAS Ctr Excellence Nanosci,Ctr Mat Sci & Optoelec, Beijing 100190, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
MONODISPERSE CYLINDRICAL MICELLES; BLOOD-VESSELS; DELIVERY; NANOPARTICLES; MECHANISM;
D O I
10.1021/jacs.8b13512
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The precise and highly efficient drug delivery of nanomedicines into lesions remains a critical challenge in clinical translational research. Here, an autocatalytic morphology transformation platform is presented for improving the tumor-specific accumulation of drugs by kinetic control. The in situ reorganization of prodrug from nanoparticle to beta-sheet fibrous structures for targeted accumulation is based on nucleation-based growth kinetics. During multiple administrations, the autocatalytic morphology transformation can be realized for skipping slow nucleating process and constructing the bulky nanoassembly instantaneously, which has been demonstrated to induce the cumulative effect of prodrug. Furthermore, the sustained drug release from fibrous prodrug depot in the tumor site inhibits the tumor growth efficiently. The autocatalytic morphology transformation strategy in vivo offers a novel perspective for targeted delivery strategy by introducing chemical kinetics and shows great potential in disease theranostics.
引用
收藏
页码:4406 / 4411
页数:6
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