Microfluidic device architecture for electrochemical patterning and detection of multiple DNA sequences

被引:61
|
作者
Pavlovic, Elizabeth [1 ]
Lai, Rebecca Y. [2 ]
Wu, Ting Ting [4 ]
Ferguson, Brian S. [3 ]
Sun, Ren [4 ]
Plaxco, Kevin W. [2 ]
Soh, H. T. [1 ,3 ]
机构
[1] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93111 USA
[2] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93111 USA
[3] Univ Calif Santa Barbara, Dept Mech Engn, Santa Barbara, CA 93111 USA
[4] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
关键词
D O I
10.1021/la702681c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical biosensors pose an attractive solution for point-of-care diagnostics because they require minimal instrumentation and they are scalable and readily integrated with microelectronics. The integration of electrochemical biosensors with microscale devices has, however, proven to be challenging due to significant incompatibilities among biomolecular stability, operation conditions of electrochemical sensors, and microfabrication techniques. Toward a solution to this problem, we have demonstrated here an electrochemical array architecture that supports the following processes in situ, within a self-enclosed microfluidic device: (a) electrode cleaning and preparation, (b) electrochemical addressing, patterning, and immobilization of sensing biomolecules at selected sensor pixels, (c) sequence-specific electrochemical detection from multiple pixels, and (d) regeneration of the sensing pixels. The architecture we have developed is general, and it should be applicable to a wide range of biosensing schemes that utilize gold-thiol self-assembled monolayer chemistry. As a proof-of-principle, we demonstrate the detection and differentiation of polymerase chain reaction (PCR) amplicons diagnostic of human (H1N1) and avian (H5N1) influenza.
引用
收藏
页码:1102 / 1107
页数:6
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