基于RFID标签的远程DNA传感系统

J. Chien, C. Tsai, Y.T. Cheng, C.R. Yang, P.Y. Wang, T.L. Chang, D.S. Lee, C. W. Chang, W.P. Chou, C. Chiang, Y.W. Lee, P. Chen
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引用次数: 3

摘要

与传统的基于聚合酶链反应(PCR)和酶联免疫吸附法(ELISA)的生化检测方法昂贵且耗时不同,本研究采用纳米金(AuNP)免疫扩增法和RFID通信平台的DNA芯片检测技术,快速方便地检测DNA序列。首先将捕获的DNA (cDNA)固定在电容器所在的底物上。然后在3'端加入带有AuNP的靶DNA (tDNA)和探针DNA (pDNA),形成多层AuNP连接结构。由于微电容间隙之间的aunp连接结构改变了电容所在介质的介电常数,串联LC电路的谐振频率立即发生位移。本研究提出的片上实验室由射频识别(RFID)系统供电。LC谐振频率的位移决定了tDNA是否存在。因此,检测芯片不需要任何其他内部电源或昂贵的仪器进行电信号测量。本研究为生物化学检测提供了一个简单、快速、方便的平台
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A RFID Tag Based Remote DNA sensing System
Different from traditional detection methods including polymerase chain reaction (PCR) based assays and enzyme-linked immunosorbent assays (ELISA) which are expensive and time consuming for biochemical analysis, in our study, a DNA chip assay using gold nanoparticle (AuNP) immunological amplification method and RFID communication platform were applied to detect DNA sequences rapidly and conveniently. First the capture DNA (cDNA) was immobilized to the substrate on which the capacitor locates. Then the target DNA (tDNA) and probe DNA (pDNA) with a AuNP at the 3' end were added to form several layers of AuNP linked structures. Since the permittivity of the medium in which the capacitor is located changed due to the AuNP-linking structures between the gaps of the microcapacitor, the resonant frequency of series LC circuit shifted immediately. The lab-on-a-chip proposed in this study was power supplied by the radiofrequency identification (RFID) system. The shift of the LC resonant frequency determined whether the tDNA existed. Thus the detection chip needed no any other internal power supply or expensive instruments for electrical signal measurement. The study provides a simple, fast and convenient platform for biochemical detection
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