GMR biosensor arrays: A system perspective

被引:121
作者
Hall, D. A. [2 ]
Gaster, R. S. [3 ,4 ]
Lin, T. [2 ]
Osterfeld, S. J. [5 ]
Han, S. [6 ]
Murmann, B. [2 ]
Wang, S. X. [1 ,2 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Med Scientist Training Program, Stanford, CA 94305 USA
[5] MagArray Inc, Sunnyvale, CA 94089 USA
[6] IBM TJ Watson Res Ctr, Yorktown Hts, NY 10598 USA
基金
美国国家科学基金会;
关键词
Magnetic biosensor; GMR biosensor; Spin-valve biosensor; Multiplexing spin-valves; SENSORS; IMMUNOASSAY;
D O I
10.1016/j.bios.2010.01.038
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Giant magnetoresistive biosensors are becoming more prevalent for sensitive, quantifiable biomolecular detection. However, in order for magnetic biosensing to become competitive with current optical protein microarray technology, there is a need to increase the number of sensors while maintaining the high sensitivity and fast readout time characteristic of smaller arrays (1-8 sensors). In this paper, we present a circuit architecture scalable for larger sensor arrays (64 individually addressable sensors) while maintaining a high readout rate (scanning the entire array in less than 4 s). The system utilizes both time domain multiplexing and frequency domain multiplexing in order to achieve this scan rate. For the implementation, we propose a new circuit architecture that does not use a classical Wheat-stone bridge to measure the small change in resistance of the sensor. Instead, an architecture designed around a transimpedance amplifier is employed. A detailed analysis of this architecture including the noise, distortion, and potential sources of errors is presented, followed by a global optimization strategy for the entire system comprising the magnetic tags, sensors, and interface electronics. To demonstrate the sensitivity, quantifiable detection of two blindly spiked samples of unknown concentrations has been performed at concentrations below the limit of detection for the enzyme-linked immunosorbent assay. Lastly, the multiplexing capability and reproducibility of the system was demonstrated by simultaneously monitoring sensors functionalized with three unique proteins at different concentrations in real-time. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2051 / 2057
页数:7
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