Ice-mediated interfacial membrane synthesis of cargo-independent microcapsules

IF 22.6 0 CHEMISTRY, MULTIDISCIPLINARY
Hongzhong Du, Jiahui Wu, Kai Yang, Chuanbiao Zhang, Dan Wang, Xiaoting Chen, Siyuan Wang, Yuchen Wu, Shuo Jin, Xiaofei Chen, Zhiyuan He
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引用次数: 0

Abstract

Membrane-defined compartmentalization enables selective transport and protects biomacromolecules in living systems, yet synthetic microcapsules remain difficult to fabricate because existing methods are often harsh, multistep or cargo-specific. Here we report an ice-mediated interfacial reaction platform that programmes membrane growth on ice-sphere templates to generate closed microcapsules with cargo-independent encapsulation. During ice recrystallization, monomers preloaded within the ice matrix are enriched into the quasi-liquid layer, where they undergo confined interfacial amidation with a complementary organic-phase monomer to form a conformal polyamide membrane. Melting the ice releases intact microcapsules with encapsulated cargo retained. The resulting microcapsules exhibit tunable membrane thicknesses (7–260 nm) and diameters (30–500 μm), and function as confined microreactors for multienzyme redox cascades, achieving up to an 80-fold enhancement in visible-light-driven CO2-to-methanol conversion. This strategy provides a mild and potentially scalable route to programmable semipermeable microcompartments.

Abstract Image

冰介导的界面膜合成与货物无关的微胶囊
膜定义的区隔化能够在生命系统中选择性运输和保护生物大分子,但合成微胶囊仍然很难制造,因为现有的方法通常苛刻,多步骤或货物特异性。在这里,我们报告了一个冰介导的界面反应平台,该平台可以在冰球模板上编程膜生长,以产生与货物无关的封闭微胶囊。在冰重结晶过程中,预加载在冰基质中的单体被富集到准液体层,在那里它们与互补的有机相单体进行受限的界面酰胺化,形成保形聚酰胺膜。融化冰释放出完整的微胶囊,并保留了被封装的货物。所得的微胶囊具有可调的膜厚度(7-260 nm)和直径(30-500 μm),并可作为多酶氧化还原级联的受限微反应器,在可见光驱动的二氧化碳到甲醇的转化中实现高达80倍的增强。这种策略为可编程半渗透微室提供了一种温和且具有潜在可扩展性的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
8.10
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