A multichannel DNA SoC for rapid point-of-care gene detection

David Garner, Hua Bai, P. Georgiou, T. Constandinou, Samuel Reed, L. Shepherd, Winston Wong, K. T. Lim, C. Toumazou
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引用次数: 62

Abstract

Point-of-care diagnostics for detection of genetic sequences require biosensing platforms that are sensitive to the target sequence, and are also fast, mass-manufacturable, and - ideally - disposable. Conventional lab-based methods of detecting DNA sequences rely on optical methods, typically by the addition of fluorescent tags to the target DNA that in turn latches onto a DNA probe sequence only if there is a match between the two. These techniques are cumbersome as they require upfront tagging of the DNA with expensive reagents and laboratory equipment to detect the optical signals. Recently, developments have been made in transferring these optical methods to inexpensive CMOS ICs [1], although the requirement for tagging remains. Magnetic beads offer an alternative means of tagging the DNA and their presence can be detected by the shift in resonant frequency of an on-chip LC tank [2]. There have also been attempts based on “label-free” electrochemical detection using FETs [3,4], but none of these have been implemented in unmodified standard CMOS.
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一个多通道DNA SoC快速点护理基因检测
检测基因序列的即时诊断需要对目标序列敏感的生物传感平台,而且要快速、可批量生产,理想情况下是一次性的。传统的实验室检测DNA序列的方法依赖于光学方法,通常是在目标DNA上添加荧光标记,只有在两者之间存在匹配时,荧光标记才会锁定在DNA探针序列上。这些技术很麻烦,因为它们需要用昂贵的试剂和实验室设备预先标记DNA来检测光信号。最近,在将这些光学方法转移到廉价的CMOS ic上取得了进展[1],尽管对标记的要求仍然存在。磁珠提供了另一种标记DNA的方法,它们的存在可以通过片上LC槽的谐振频率的变化来检测[2]。也有人尝试使用fet进行“无标签”电化学检测[3,4],但这些都没有在未经修改的标准CMOS中实现。
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