Microfabrication of single-use plastic microfluidic devices for high-throughput screening and DNA analysis

2002 ◽  
Vol 7 (5-6) ◽  
pp. 265-268 ◽  
Author(s):  
A. Gerlach ◽  
G. Knebel ◽  
A.E. Guber ◽  
M. Heckele ◽  
D. Herrmann ◽  
...  
Foods ◽  
2020 ◽  
Vol 9 (9) ◽  
pp. 1269
Author(s):  
Vojtech Hrbek ◽  
Kamila Zdenkova ◽  
Diliara Jilkova ◽  
Eliska Cermakova ◽  
Monika Jiru ◽  
...  

Two alternative, complementary analytical strategies were successfully used to identify the most common meat species—beef, pork and chicken—in meat products. The first innovative high-throughput approach was based on triacylglycerols fingerprinting by direct analysis in real time coupled with high-resolution mass spectrometry (DART–HRMS). The second was the classic commonly used DNA analysis based on the use of nuclear or mitochondrial DNA in multiplex polymerase chain reaction (mPCR). The DART–HRMS method represents a rapid, high throughput screening method and was shown to have a good potential for the authentication of meat products. Nevertheless, it should be noted that due to a limited number of samples in this pilot study, we present here a proof of concept. More samples must be analyzed by DART–HRMS to build a robust classification model applicable for reliable authentication. To verify the DART–HRMS results, all samples were analyzed by PCRs. Good compliance in samples classification was documented. In routine practice under these conditions, screening based on DART–HRMS could be used for identification of suspect samples, which could be then examined and validated by accurate PCRs. In this way, saving of both labor and cost could be achieved. In the final phase, commercially available meat products from the Czech market were tested using this new strategy. Canned meats—typical Czech sausages and luncheon meats, all with declared content of beef, pork and chicken meat—were used. Compliance with the label declaration was confirmed and no adulteration was found.


2012 ◽  
Vol 45 (10) ◽  
pp. 306-310
Author(s):  
C-C. Lee ◽  
S.M. Scott ◽  
Z. Ali

There have been considerable advances in the development of microfluidic devices that can carry out the automated and sophisticated processing necessary for DNA analysis and forensic biology. Polymer substrates with high replication techniques are often used in the manufacture of microfluidic devices that are single use, low cost and disposable. High replication techniques require the creation of a master mould from which the devices are subsequently fabricated. This review will describe the use of high replication techniques for device fabrication, with a focus on creation of the master mould manufacture and application of these devices in molecular diagnostics for forensic applications.


2006 ◽  
Vol 950 ◽  
Author(s):  
Zhengshan Zhao ◽  
Gerardo A. Diaz-Quijada ◽  
Régis Peytavi ◽  
Éric LeBlanc ◽  
Johanne Frenette ◽  
...  

ABSTRACTMicroarrays have become one of the most convenient tools for high throughput screening and have catalyzed major advances in genomics and proteomics. Other important applications can be found in medical diagnostics, detection of biothreats, drug discovery, etc. Integration of microarrays with microfluidic devices can be highly advantageous in terms of portability, shorter analysis time and lower consumption of expensive biological analytes. Since fabrication of microfluidic devices using traditional materials such as glass is rather expensive, there is a high interest in employing polymeric materials as a low cost alternative suitable for mass production. We present proof-of-concept DNA arrays on a plastic platform for the detection of four important respiratory pathogens: Influenza A virus, respiratory syncytial virus, human enterovirus, and human metapneumovirus.This was accomplished by amplifying the genetic material from the viruses and simultaneously labeling the amplicons with a fluorescent dye (Cy3) via a highly sensitive multiplex Reverse Transcription Polymerase Chain Reaction (RT-PCR). The resultant RT-PCR product was hybridized, without further purification, with an array of specific oligonucleotide probes (20 mers) that had been covalently bound to a plastic substrate. Results indicate a high signal to background ratio that is comparable to commercially available microarray glass slides. In addition, 5 minute hybridization on this plastic substrate has been demonstrated using a centrifugal microfluidic platform, paving the way to a rapid medical diagnostic device for point-of-care use that is based on a low-cost portable Micro-Total-Analysis-System (μ-TAS).


2014 ◽  
Vol 86 (19) ◽  
pp. 9570-9575 ◽  
Author(s):  
Ryo Oyobiki ◽  
Taisuke Kato ◽  
Michinobu Katayama ◽  
Ai Sugitani ◽  
Takeshi Watanabe ◽  
...  

Lab on a Chip ◽  
2010 ◽  
Vol 10 (3) ◽  
pp. 341-348 ◽  
Author(s):  
Sarvesh Upadhyaya ◽  
P. Ravi Selvaganapathy

2005 ◽  
Vol 897 ◽  
Author(s):  
Gerardo Antonio Diaz-Quijada ◽  
Regis Peytavi ◽  
André Nantel ◽  
Emmanuel Roy ◽  
Michel G. Bergeron ◽  
...  

AbstractMicroarrays have become one of the most convenient tools for high throughput screening, supporting major advances in genomics and proteomics. Other important applications can be found in medical diagnostics, detection of biothreats, drug discovery, etc. Integration of microarrays with microfluidic devices can be highly advantageous in terms of portability, shorter analysis time and lower consumption of expensive biological analytes. Since fabrication of microfluidic devices using traditional materials such as glass is rather expensive, there is a high interest in employing polymeric materials as a low cost alternative that is suitable for mass production. A number of commercially available plastic materials were reviewed for this purpose and poly(methylmethacrylate) and Zeonor™ 1060R were identified as promising candidates, for which methods for surface modification and covalent immobilization of DNA oligonucleotide were developed. In addition, we present proof-of-concept plastic-based microarrays with and without integration with microfluidics.


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