Light-Dominated Reversible Shape Transformation of Block Copolymer Particles under Emulsion Droplets

IF 5.2 Q1 POLYMER SCIENCE
Dan Ji, Zihao Zhang, Qianyao Liu, Xiaohua Chang* and Yutian Zhu*, 
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引用次数: 0

Abstract

Shape-morphing particles that can switch their shapes in response to environmental stimuli have attracted considerable focus given their capacity to enhance the functionality of smart materials. However, shape-switching particles sensitive to light are rarely reported. Herein, a robust and facile strategy for the production of photoresponsive block copolymer (BCP) assemblies is developed via three-dimensional restricted coassembly of polystyrene-b-poly(4-vinylpyridine) (PS-b-P4VP) and azobenzene (Azo)-based photoactive additives under emulsion droplets. Upon alternating exposure to ultraviolet and visible light, trans–cis isomerization of the Azo group causes the hydrophobic–hydrophilic transition of Azo within the P4VP phases. Therefore, the particle shape and internal nanostructure could be reversely modulated between an onion shape with a PS outer layer and an inverted onion with P4VP at the interface. Notably, the light-driven morphological behavior of BCP assemblies exhibits promising potential in controlled drug release, which positions them as compelling candidates for advanced biomedical and clinical systems.

Abstract Image

乳液滴下嵌段共聚物颗粒光主导的可逆形状转变。
由于能够增强智能材料的功能,能够根据环境刺激改变形状的变形粒子已经引起了相当大的关注。然而,对光敏感的形状转换粒子很少被报道。本文通过在乳液滴下聚苯乙烯-b-聚(4-乙烯基吡啶)(PS-b-P4VP)和偶氮苯(Azo)基光活性添加剂的三维受限共组装,开发了一种强大而简便的生产光响应嵌段共聚物(BCP)组装体的策略。在紫外和可见光交替照射下,偶氮基团的反式异构化导致偶氮在P4VP相内发生疏水-亲水转变。因此,颗粒形状和内部纳米结构可以在具有PS外层的洋葱形状和界面处具有P4VP的倒洋葱之间进行反向调制。值得注意的是,BCP组件的光驱动形态行为在控制药物释放方面显示出很大的潜力,这使它们成为先进生物医学和临床系统的有力候选者。
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来源期刊
CiteScore
10.40
自引率
3.40%
发文量
209
审稿时长
1 months
期刊介绍: ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science. With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.
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