Electrical Detection of Nucleic Acid Amplification Using an On-Chip Quasi-Reference Electrode and a PVC REFET

被引:38
|
作者
Salm, Eric [1 ,2 ]
Zhong, Yu [2 ,3 ]
Reddy, Bobby, Jr. [2 ,3 ]
Duarte-Guevara, Carlos [2 ,3 ]
Swaminathan, Vikhram [2 ,4 ]
Liu, Yi-Shao [5 ]
Bashir, Rashid [1 ,2 ,3 ]
机构
[1] Univ Illinois, Dept Bioengn, Urbana, IL 61801 USA
[2] Micro & Nanotechnol Lab, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Elect & Comp Engn, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Mech Sci & Engn, Urbana, IL 61801 USA
[5] Taiwan Semicond Mfg Co, Hsinchu, Taiwan
基金
美国农业部;
关键词
DNA-POLYMERASE REACTIONS; FIELD-EFFECT TRANSISTORS; REAL-TIME; PCR; OXIDES;
D O I
10.1021/ac500897t
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electrical detection of nucleic acid amplification through pH changes associated with nucleotide addition enables miniaturization, greater portability of testing apparatus, and reduced costs. However, current ion-sensitive field effect transistor methods for sensing nucleic acid amplification rely on establishing the fluid gate potential with a bulky, difficult to microfabricate reference electrode that limits the potential for massively parallel reaction detection. Here we demonstrate a novel method of utilizing a microfabricated solid-state quasi-reference electrode (QRE) paired with a pH-insensitive reference field effect transistor (REFET) for detection of real-time pH changes. The end result is a 0.18 mu m, silicon-on-insulator, foundry-fabricated sensor that utilizes a platinum QRE to establish a pH-sensitive fluid gate potential and a PVC membrane REFET to enable pH detection of loop mediated isothermal amplification (LAMP). This technique is highly amendable to commercial scale-up, reduces the packaging and fabrication requirements for ISFET pH detection, and enables massively parallel droplet interrogation for applications, such as monitoring reaction progression in digital PCR.
引用
收藏
页码:6968 / 6975
页数:8
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