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基于盐-油协同机制的原型介孔UiO-66(Zr)

Archetype Mesoporous UiO-66(Zr) Enabled by the Salt-Oil Synergetic Mechanism.

作者信息

Yang Jian, Shang Qinlu, Li Jiana, Qiu Junzheng, Tu Ming, Tong Yao, Gu Jinlou

机构信息

Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.

出版信息

JACS Au. 2025 Jun 29;5(7):3299-3310. doi: 10.1021/jacsau.5c00440. eCollection 2025 Jul 28.

DOI:10.1021/jacsau.5c00440
PMID:40747073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12308434/
Abstract

Despite that prototype hierarchically mesoporous UiO-66-(Zr) (HMUiO-66-(Zr)) integrates coupled micropores and mesopores within a single crystal, there are few, if any, reports on the direct construction of such a material with exceptional chemical and thermal stability. Herein, a salt-oil synergetic mechanism was proposed to rationalize the soft-template-directed assembly of prototype HMUiO-66-(Zr) under mild conditions. The salts significantly lowered the crystallization temperature of UiO-66-(Zr) in the aqueous phase, while the oil phase enhanced the stability of the soft-template aggregate at elevated temperatures, making the assembly environment of crystal and template phases gradually compatible. The synergy between salts and the oil phase enabled precise control over mesopore sizes and texture of HMMOFs as salting-out and salting-in ions influenced emulsion swelling and resulted in a different mesopore structure. Based on the tunable mesopores and excellent stability of HMUiO-66-(Zr), a versatile platform was obtained for the loading of various enzymes and specific recognition toward their metabolic substrates. By matching the mesopore size to accommodate dehydrogenases and NAD, various probes were designed for detecting biomarkers of diabetic acidosis, including β-hydroxybutyrate, glucose, l-lactate, and d-lactate. These probes were integrated into a sensing array, which enabled the simultaneous detection and correlation analysis of these biomarkers, effectively distinguishing different types of diabetic acidosis.

摘要

尽管原型分层介孔UiO-66-(Zr)(HMUiO-66-(Zr))在单晶中整合了耦合的微孔和介孔,但关于直接构建具有出色化学和热稳定性的这种材料的报道极少(如果有的话)。在此,提出了一种盐-油协同机制,以合理化在温和条件下软模板导向的原型HMUiO-66-(Zr)的组装。盐显著降低了UiO-66-(Zr)在水相中的结晶温度,而油相在升高的温度下增强了软模板聚集体的稳定性,使晶体相和模板相的组装环境逐渐兼容。盐和油相之间的协同作用能够精确控制HMMOFs的介孔尺寸和织构,因为盐析和盐溶离子影响乳液膨胀并导致不同的介孔结构。基于HMUiO-66-(Zr)可调谐的介孔和出色的稳定性,获得了一个用于负载各种酶并对其代谢底物进行特异性识别的通用平台。通过匹配介孔尺寸以容纳脱氢酶和NAD,设计了各种探针来检测糖尿病酸中毒的生物标志物,包括β-羟基丁酸酯、葡萄糖、L-乳酸和D-乳酸。这些探针被整合到一个传感阵列中,该阵列能够对这些生物标志物进行同时检测和相关性分析,有效区分不同类型的糖尿病酸中毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/ce61f53215bc/au5c00440_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/e148034c8f83/au5c00440_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/ed8cf78a7528/au5c00440_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/2022b9e83d6a/au5c00440_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/3155ae02e2ca/au5c00440_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/b691eb6999f9/au5c00440_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/ce61f53215bc/au5c00440_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/e148034c8f83/au5c00440_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/ed8cf78a7528/au5c00440_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/2022b9e83d6a/au5c00440_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/3155ae02e2ca/au5c00440_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/b691eb6999f9/au5c00440_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/12308434/ce61f53215bc/au5c00440_0006.jpg

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本文引用的文献

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