Microstructuring of polymer films for sensitive genotyping by real-time PCR on a centrifugal microfluidic platform

被引:101
作者
Focke, Maximilian [1 ]
Stumpf, Fabian [1 ]
Faltin, Bernd [1 ]
Reith, Patrick [1 ]
Bamarni, Dylan [1 ]
Wadle, Simon [1 ]
Mueller, Claas [2 ,3 ]
Reinecke, Holger [2 ,3 ,4 ]
Schrenzel, Jacques [5 ,6 ]
Francois, Patrice [5 ]
Mark, Daniel [4 ]
Roth, Guenter [1 ,4 ]
Zengerle, Roland [1 ,3 ,4 ]
von Stetten, Felix [1 ,4 ]
机构
[1] Univ Freiburg, Lab MEMS Applicat, Dept Microsyst Engn IMTEK, D-79110 Freiburg, Germany
[2] Univ Freiburg, Lab Proc Technol, Dept Microsyst Engn IMTEK, D-79110 Freiburg, Germany
[3] Univ Freiburg, Ctr Biol Signalling Studies Bioss, D-7800 Freiburg, Germany
[4] HSG IMIT, D-78052 Villingen Schwenningen, Germany
[5] Univ Hosp Geneva, Genom Res Lab, CH-1211 Geneva, Switzerland
[6] Univ Hosp Geneva, Clin Microbiol Lab, CH-1211 Geneva, Switzerland
关键词
STAPHYLOCOCCUS-AUREUS;
D O I
10.1039/c004954a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present a novel process flow enabling prototyping of microfluidic cartridges made out of polymer films. Its high performance is proven by implementation of a microfluidic genotyping assay testing 22 DNA samples including clinical isolates from patients infected by methicilin-resistant Staphylococcus aureus (MRSA). The microfluidic cartridges (disks) are fabricated by a novel process called microthermoforming by soft lithography (mu TSL). Positive moulds are applied allowing for higher moulding precision and very easy demoulding when compared to conventional microthermoforming. High replication accuracies with geometric disk-to-disk variations of less than 1% are typical. We describe and characterise fabrication and application of microfluidic cartridges with wall thicknesses <188 mu m thus enabling efficient thermocycling during real-time polymerase chain reaction (PCR). The microfluidic cartridges are designed for operation in a slightly modified commercial thermocycling instrument. This approach demonstrates new opportunities for both microfluidic developments and well-established laboratory instruments. The microfluidic protocol is controlled by centrifugal forces and divides the liquid sample parallely into independent aliquots of 9.8 mu l (CV 3.4%, N = 32 wells). The genotyping assays are performed with pre-stored primers and probes for real-time PCR showing a limit of detection well below 10 copies of DNA per reaction well (N = 24 wells in 3 independent disks). The system was evaluated by 44 genotyping assays comprising 22 DNA samples plus duplicates in a total of 11 disks. The samples contained clinical samples of seven different genotypes of MRSA as well as positive and negative controls. The results are in excellent agreement with the reference in microtubes.
引用
收藏
页码:2519 / 2526
页数:8
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