Thom Nicole K, Lewis Gregory G, Yeung Kimy, Phillips Scott T
Department of Chemistry, The Pennsylvania State University, University Park, PA 16802, USA; ; Tel: 814 867 2502.
RSC Adv. 2014 Jan 1;4(3):1334-1340. doi: 10.1039/C3RA44717K.
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.
荧光检测通常需要专门的设备,因此在资源有限的环境中不易实施。在此,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,同时使用配备摄像头的手机来捕获荧光响应并对检测进行定量。使用基于纸的微流控装置可实现荧光检测,该装置包含内部流体电池、表面贴装发光二极管、一段2毫米长的透明吸管作为比色皿,以及一种经过适当设计的小分子试剂,该试剂在暴露于特定酶生物标志物时会从弱荧光转变为强荧光。通过使用配备摄像头的手机拍摄检测区域,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,以提供灵敏且定量的结果。在一个30分钟的模型检测中,酶β-D-半乳糖苷酶的定量检测下限达到700皮摩尔水平。本通讯描述了基于纸的微流控装置中这类检测的设计,并表征了影响该技术灵敏度和重现性的关键参数。