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面向液-纳米-液界面的各向异性封装。

Liquid-nano-liquid interface-oriented anisotropic encapsulation.

作者信息

Zhan Yating, Huang Xirui, Liu Minchao, Lin Runfeng, Yu Hongyue, Kou Yufang, Xing Enyun, Elzatahry Ahmed A, Mady Mohamed F, Zhao Dongyuan, Zhao Tiancong, Li Xiaomin

机构信息

Department of Chemistry, State Key Laboratory of Molecular Engineering of Polymers, College of Chemistry and Materials, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, China.

William A. Brookshire Department of Chemical and Biomolecular Engineering, Cullen College of Engineering, University of Houston, Houston, TX 77204.

出版信息

Proc Natl Acad Sci U S A. 2025 Jan 7;122(1):e2417292121. doi: 10.1073/pnas.2417292121. Epub 2024 Dec 30.

Abstract

Emulsion interface engineering has been widely employed for the synthesis of nanomaterials with various morphologies. However, the instability of the liquid-liquid interface and uncertain interfacial interactions impose significant limitations on controllable fabrications. Here, we developed a liquid-nano-liquid interface-oriented anisotropic encapsulation strategy for fabricating asymmetric nanohybrids. Specifically, functional nanoparticles such as magnetic nanoparticles, lanthanide fluorescent nanoparticles, and Au nanorods were anisotropically encapsulated by mesoporous polydopamine (mPDA). In this emulsion system, the wetting behavior of functional nanoparticles at the water/oil interface could be manipulated by the stabilizer of the emulsion (surfactant), leading to the anisotropic assembly of mPDA shell and resulting in various nanostructures, including core-shell, yolk-shell with small opening, ball-in-bowl, and multipetal structures. Due to their structural asymmetry, inherent magnetic properties, and photothermal properties, the ball-in-bowl structured FeO@SiO&mPDA nanohybrids, serving as proof of concept for nanomotors, demonstrated effective penetration of bacterial biofilm and promotion of infected wound healing. Overall, our approach offers a different perspective for designing morphologically controllable asymmetric structures based on liquid-nano-liquid interface in microemulsion systems that hold great potential for establishing innovative functional nanomaterials.

摘要

乳液界面工程已被广泛用于合成具有各种形态的纳米材料。然而,液-液界面的不稳定性和不确定的界面相互作用对可控制备造成了重大限制。在此,我们开发了一种面向液-纳米-液界面的各向异性封装策略来制备不对称纳米杂化物。具体而言,磁性纳米颗粒、镧系荧光纳米颗粒和金纳米棒等功能性纳米颗粒被介孔聚多巴胺(mPDA)各向异性封装。在该乳液体系中,功能性纳米颗粒在水/油界面的润湿行为可通过乳液稳定剂(表面活性剂)进行调控,从而导致mPDA壳层的各向异性组装,并产生各种纳米结构,包括核壳结构、带小开口的蛋黄壳结构、碗中球结构和多花瓣结构。由于其结构不对称性、固有磁性和光热性质,碗中球结构的FeO@SiO&mPDA纳米杂化物作为纳米马达的概念验证,展示了对细菌生物膜的有效穿透和对感染伤口愈合的促进作用。总体而言,我们的方法为基于微乳液体系中液-纳米-液界面设计形态可控的不对称结构提供了一个不同的视角,这对于建立创新的功能性纳米材料具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56b7/11725832/8ea636c8a394/pnas.2417292121fig01.jpg

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