Fast nucleic acid amplification for integration in point-of-care applications

被引:21
作者
Brunklaus, Sabine [1 ]
Hansen-Hagge, Thomas E. [2 ]
Erwes, Julia [1 ]
Hoeth, Julian [1 ]
Jung, Mathieu [1 ]
Latta, Daniel [1 ]
Strobach, Xenia [1 ]
Winkler, Christian [1 ]
Ritzi-Lehnert, Marion [1 ]
Drese, Klaus S. [1 ]
机构
[1] Inst Mikrotech Mainz GmbH, D-55129 Mainz, Germany
[2] Microfluid ChipShop, Jena, Germany
关键词
Lab-on-a-chip; Microfluidics; PCR; POLYMERASE-CHAIN-REACTION; PCR; DNA;
D O I
10.1002/elps.201200259
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An ultrafast microfluidic PCR module (30 PCR cycles in 6 min) based on the oscillating fluid plug concept was developed. A robust amplification of native genomic DNA from whole blood samples could be achieved at operational conditions established from systematic investigations of key parameters including heat transfer and in particular flow velocities. Experimental data were augmented with results from computational fluid dynamics simulations. The reproducibility of the current system was substantially improved compared to previous concepts by integration of a closed reservoir instead of utilizing a vented channel end at ambient pressure rendering the devised module suitable for integration into complex sample-to-answer analysis platforms such as point-of-care applications.
引用
收藏
页码:3222 / 3228
页数:7
相关论文
共 30 条
[1]   Miniaturised nucleic acid analysis [J].
Auroux, PA ;
Koc, Y ;
deMello, A ;
Manz, A ;
Day, PJR .
LAB ON A CHIP, 2004, 4 (06) :534-546
[2]   Design and theoretical evaluation of a novel microfluidic device to be used for PCR [J].
Bu, MQ ;
Melvin, T ;
Ensell, G ;
Wilkinson, JS ;
Evans, AGR .
JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 2003, 13 (04) :S125-S130
[3]   Performing microchannel temperature cycling reactions using reciprocating reagent shuttling along a radial temperature gradient [J].
Cheng, JY ;
Hsieh, CJ ;
Chuang, YC ;
Hsieh, JR .
ANALYST, 2005, 130 (06) :931-940
[4]   Polymerase chain reaction in polymeric microchips:: DNA amplification in less than 240 seconds [J].
Giordano, BC ;
Ferrance, J ;
Swedberg, S ;
Hühmer, AFR ;
Landers, JP .
ANALYTICAL BIOCHEMISTRY, 2001, 291 (01) :124-132
[5]  
Hagan KA, 2011, LAB CHIP, V11, P957, DOI [10.1039/c0lc00136h, 10.1039/c01c00136h]
[6]   Currently used nucleic acid amplification tests for the detection of viruses and atypicals in acute respiratory infections [J].
Ieven, Margareta .
JOURNAL OF CLINICAL VIROLOGY, 2007, 40 (04) :259-276
[7]   Helical flows and chaotic mixing in curved micro channels [J].
Jiang, F ;
Drese, KS ;
Hardt, S ;
Küpper, M ;
Schönfeld, F .
AICHE JOURNAL, 2004, 50 (09) :2297-2305
[8]  
Jung M., 2011, P SOC PHOTO-OPT INS, V7929
[9]   A scalable and modular lab-on-a-chip genetic analysis instrument [J].
Kaigala, G. V. ;
Behnam, M. ;
Bidulock, A. C. E. ;
Bargen, C. ;
Johnstone, R. W. ;
Elliott, D. G. ;
Backhouse, C. J. .
ANALYST, 2010, 135 (07) :1606-1617
[10]   Chemical amplification: Continuous-flow PCR on a chip [J].
Kopp, MU ;
de Mello, AJ ;
Manz, A .
SCIENCE, 1998, 280 (5366) :1046-1048