Recent Progress in Fluorescent Vesicles with Aggregation-induced Emission

被引:24
作者
Chen, Hui [1 ]
Li, Min-Hui [1 ,2 ]
机构
[1] PSL Univ Paris, CNRS, Inst Rech Chim Paris, Chim ParisTech, F-75005 Paris, France
[2] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Vesicles; Polymersomes; Aggregation-induced emission; Small-molecule amphiphiles; Amphiphilic polymers; Amphiphilic supramolecules; Amphiphilic supramacromolecules; DRUG-DELIVERY; NANOPARTICLES; POLYMERSOMES; FABRICATION; COPOLYMER; SENSOR; CONSTRUCTION; LUMINESCENCE; LIPOSOMES;
D O I
10.1007/s10118-019-2204-5
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Fluorescent vesicles have recently attracted increasing attention because of their potential applications in bioimaging, diagnostics, and theranostics, for example, in vivo study of the delivery and the distribution of active substances. However, fluorescent vesicles containing conventional organic dyes often suffer from the problem of aggregation-caused quenching (ACQ) of fluorescence. Fluorescent vesicles working with aggregation-induced emission (AIE) offer an extraordinary tool to tackle the ACQ issue, showing advantages such as high emission efficiency, superior photophysical stability, low background interference, and high sensitivity. AIE fluorescent vesicles represent a new type of fluorescent and functional nanomaterials. In this review, we summarize the recent advances in the development of AIE fluorescent vesicles. The review is organized according to the chemical structures and architectures of the amphiphilic molecules that constitute the AIE vesicles, i.e., small-molecule amphiphiles, amphiphilic polymers, and amphiphilic supramolecules and supramacromolecules. The studies on the applications of these AIE vesicles as stimuli-responsive vesicles, fluorescence-guided drug release carriers, cell imaging tools, and fluorescent materials based on fluorescence resonance energy transfer (FRET) are also discussed.
引用
收藏
页码:352 / 371
页数:20
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