Document Detail


A microchip device for enhancing capillary zone electrophoresis using pressure-driven backflow.
MedLine Citation:
PMID:  23092536     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
A reduction in electroosmotic flow (EOF) is often desirable in glass microchannels for realizing high resolutions in capillary zone electrophoresis (CZE). While static and dynamic coatings have been commonly employed to accomplish this goal, such chemicals can introduce unwanted interactions of the analyte molecules with the separation medium and/or channel surface. In this article, we report a microfluidic device that can enhance the resolving power of CZE analysis by generating a pressure-driven backflow in the separation channel. This backflow was generated in our current work by fabricating a shallow segment (0.5-4 µm deep) downstream of the separation duct (5µm deep) and applying an electric field across it. A mismatch in EOF transport rate at the interface of this segment was shown to yield a pressure-gradient that counteracted electroosmosis and diminished the net fluid flow in the separation conduit by nearly an order of magnitude. Although the resulting pressure-driven backflow also somewhat increased the band broadening in the analysis channel, overall it allowed us to separate an amino acid mixture with an 8-fold higher resolution. The microchip device presented here is particularly suitable for miniaturization of the CZE method and is easily integrable to other analytical procedures making it an attractive module for lab-on-a-chip applications.
Authors:
Ling Xia; Debashis Dutta
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Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-10-23
Journal Detail:
Title:  Analytical chemistry     Volume:  -     ISSN:  1520-6882     ISO Abbreviation:  Anal. Chem.     Publication Date:  2012 Oct 
Date Detail:
Created Date:  2012-10-24     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0370536     Medline TA:  Anal Chem     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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