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Quantitative Fluorescence Assays Using a Self-Powered Paper-Based Microfluidic Device and a Camera-Equipped Cellular Phone

机译:使用自供电纸基微流控设备和配备摄像头的手机进行荧光定量分析

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摘要

Fluorescence assays often require specialized equipment and, therefore, are not easily implemented in resource-limited environments. Herein we describe a point-of-care assay strategy in which fluorescence in the visible region is used as a readout, while a camera-equipped cellular phone is used to capture the fluorescent response and quantify the assay. The fluorescence assay is made possible using a paper-based microfluidic device that contains an internal fluidic battery, a surface-mount LED, a 2-mm section of a clear straw as a cuvette, and an appropriately-designed small molecule reagent that transforms from weakly fluorescent to highly fluorescent when exposed to a specific enzyme biomarker. The resulting visible fluorescence is digitized by photographing the assay region using a camera-equipped cellular phone. The digital images are then quantified using image processing software to provide sensitive as well as quantitative results. In a model 30 min assay, the enzyme β-D-galactosidase was measured quantitatively down to 700 pM levels. This Communication describes the design of these types of assays in paper-based microfluidic devices and characterizes the key parameters that affect the sensitivity and reproducibility of the technique.
机译:荧光分析通常需要专门的设备,因此在资源有限的环境中不容易实现。在这里,我们描述了一种即时检测策略,其中可见光区域的荧光用作读数,而配备摄像头的手机则用于捕获荧光响应并量化检测。使用基于纸的微流控设备可以进行荧光分析,该设备包括内部流体电池,表面安装的LED,2毫米长的透明吸管作为比色皿,以及经过适当设计的从当暴露于特定的酶生物标记时,荧光强度从弱到高。通过使用配备相机的手机拍摄化验区域,可以将产生的可见荧光数字化。然后使用图像处理软件对数字图像进行定量,以提供敏感的定量结果。在30分钟的模型分析中,定量测量了酶β-D-半乳糖苷酶,直至700 pM的水平。本交流介绍了纸质微流控设备中这些类型分析的设计,并描述了影响该技术的灵敏度和可重复性的关键参数。

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