Literature DB >> 21909803

A plastic, disposable microfluidic flow cell for coupled on-chip PCR and microarray detection of infectious agents.

Christopher G Cooney1, David Sipes, Nitu Thakore, Rebecca Holmberg, Phillip Belgrader.   

Abstract

Clinical laboratories are recognizing the importance of implementing sensitive and specific molecular diagnostic tests. However, widespread adoption of these tests requires simplified workflows without requiring expensive supporting instrumentation. To enable microarray-based analysis to meet these requirements, we describe a valveless flow cell for disposable use that supports PCR coupled with microarray hybridization in the same chamber. The flow cell assembly consists simply of double-faced tape, a plastic microarray substrate, an absorbent, and a commercially-available hydrophilic thin film. The simple construction lends itself to low-cost and ease of manufacturing, yet several features reduce the complexity of the standard microarray workflow. First, there is no requirement for custom instrumentation. Second, the hydrophilic thin film allows uniform filling of a microfluidic chamber. Third, a geometric capillary stop design confines liquid to the microarray chamber during PCR, and thus eliminates the need for a valve or hydrophobic surface treatment. And fourth, imbibition drives the uniform removal of liquid reagents from the array chamber. Three hundred genomic copies of methicillin-resistant Staphylococcus aureus (MRSA) are detected in a flow cell with gel drop microarrays printed on an unmodified plastic substrate. This sensitivity is shown to be comparable to conventional methods (i.e., PCR in a tube, with separate hybridization in a microarray chamber, where amplicon is exposed to the workspace before and after hybridization). However, the flow cell combines these multiple steps into a simple, compact workflow without the need for complex valves or custom instrumentation and is less susceptible to contamination of the workspace than conventional methods because the amplicon is confined to the device.

Entities:  

Mesh:

Year:  2012        PMID: 21909803      PMCID: PMC5882199          DOI: 10.1007/s10544-011-9584-9

Source DB:  PubMed          Journal:  Biomed Microdevices        ISSN: 1387-2176            Impact factor:   2.838


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2.  Microfluidic large-scale integration.

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3.  DNA amplification and hybridization assays in integrated plastic monolithic devices.

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4.  Phase change microvalve for integrated devices.

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6.  Clinical applications of whole-blood PCR with real-time instrumentation.

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8.  Thermoelectric manipulation of aqueous droplets in microfluidic devices.

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9.  An integrated nanoliter DNA analysis device.

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10.  Centrifugo-pneumatic valve for metering of highly wetting liquids on centrifugal microfluidic platforms.

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  12 in total

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2.  Development and clinical testing of a simple, low-density gel element array for influenza identification, subtyping, and H275Y detection.

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3.  An automated microfluidic system for single-stranded DNA preparation and magnetic bead-based microarray analysis.

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4.  Demonstrating a multi-drug resistant Mycobacterium tuberculosis amplification microarray.

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5.  Profiling in situ microbial community structure with an amplification microarray.

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6.  Simplified microarray system for simultaneously detecting rifampin, isoniazid, ethambutol, and streptomycin resistance markers in Mycobacterium tuberculosis.

Authors:  Yvonne Linger; Alexander Kukhtin; Julia Golova; Alexander Perov; Amine Lambarqui; Lexi Bryant; George B Rudy; Kim Dionne; Stefanie L Fisher; Nicole Parrish; Darrell P Chandler
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7.  Structured oligonucleotides for target indexing to allow single-vessel PCR amplification and solid support microarray hybridization.

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8.  A Benchtop Automated Sputum-to-Genotype System Using a Lab-on-a-Film Assembly for Detection of Multidrug-Resistant Mycobacterium tuberculosis.

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9.  Laboratory Evaluation of a Lateral-Flow Cell for Molecular Detection of First-Line and Second-Line Antituberculosis Drug Resistance.

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Review 10.  Infectious Disease Management through Point-of-Care Personalized Medicine Molecular Diagnostic Technologies.

Authors:  Luc Bissonnette; Michel G Bergeron
Journal:  J Pers Med       Date:  2012-05-02
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