An integrated CMOS quantitative-polymerase-chain-reaction lab-on-chip for point-of-care diagnostics

被引:81
作者
Norian, Haig [1 ]
Field, Ryan M. [1 ]
Kymissis, Ioannis [1 ]
Shepard, Kenneth L. [1 ]
机构
[1] Columbia Univ, Dept Elect Engn, New York, NY 10027 USA
基金
美国国家科学基金会;
关键词
ELECTROWETTING-BASED ACTUATION; A-CHIP; PCR; CIRCUITS; DROPLETS; MICROFLUIDICS; AMPLIFICATION;
D O I
10.1039/c4lc00443d
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Considerable effort has recently been directed toward the miniaturization of quantitative-polymerase-chain-reaction (qPCR) instrumentation in an effort to reduce both cost and form factor for point-of-care applications. Considerable gains have been made in shrinking the required volumes of PCR reagents, but resultant prototypes retain their bench-top form factor either due to heavy heating plates or cumbersome optical sensing instrumentation. In this paper, we describe the use of complementary-metal-oxide semiconductor (CMOS) integrated circuit (IC) technology to produce a fully integrated qPCR lab-on-chip. Exploiting a 0.35 mu m high-voltage CMOS process, the IC contains all of the key components for performing qPCR. Integrated resistive heaters and temperature sensors regulate the surface temperature of the chip to an accuracy of 0.45 degrees C. Electrowetting-on-dielectric microfluidics are actively driven from the chip surface, allowing for droplet generation and transport down to volumes less than 1.2 nanoliter. Integrated single-photon avalanche diodes (SPADs) are used for fluorescent monitoring of the reaction, allowing for the quantification of target DNA with more than four-orders-of-magnitude of dynamic range and sensitivities down to a single copy per droplet. Using this device, reliable and sensitive real-time proof-of-concept detection of Staphylococcus aureus (S. aureus) is demonstrated.
引用
收藏
页码:4076 / 4084
页数:9
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