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通过荧光显微镜对微流控芯片内亲水性空间异质性进行原位可视化。

In situ visualization of hydrophilic spatial heterogeneity inside microfluidic chips by fluorescence microscopy.

作者信息

Tian Rui, Li Kaitao, Shi Wenying, Ding Caifeng, Lu Chao

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China.

出版信息

Lab Chip. 2019 Mar 13;19(6):934-940. doi: 10.1039/c8lc01336e.

Abstract

Fluorescence visualization for hydrophilic spatial heterogeneity inside microfluidic chips is a long-standing challenge owing to the lack of fluorescent dyes with high contrast between the target and the background noise. Herein, we used boronic acid in aggregation-induced emission (AIE) molecules as an anchor group towards modified hydroxyl groups, and an in situ visualization approach for hydrophilic spatial heterogeneity inside microfluidic chips was demonstrated. This success is based on the high-contrast of fluorescent behaviors for AIE molecules in aqueous solution and their immobilization by hydroxyl groups inside the microfluidic channels. In comparison to conventional laboratory-based ex situ techniques, the proposed strategy provides a direct representation for hydrophilic spatial heterogeneity, including the quantity and distribution of hydroxyl groups. This discovery not only identifies a previously unknown variability in hydrophilic spatial heterogeneity inside microfluidic channels, but also guides an optimal hydrophilic modification method in the channels.

摘要

由于缺乏在目标与背景噪声之间具有高对比度的荧光染料,微流控芯片内亲水性空间异质性的荧光可视化一直是一项长期挑战。在此,我们将聚集诱导发光(AIE)分子中的硼酸用作修饰羟基的锚定基团,并展示了一种用于微流控芯片内亲水性空间异质性的原位可视化方法。这一成功基于AIE分子在水溶液中的荧光行为的高对比度以及它们在微流控通道内被羟基固定的情况。与传统的基于实验室的非原位技术相比,所提出的策略为亲水性空间异质性提供了直接表征,包括羟基的数量和分布。这一发现不仅揭示了微流控通道内亲水性空间异质性中以前未知的变异性,还指导了通道内的最佳亲水性修饰方法。

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