Microchip-Based Electrophoretic Separations with a Pressure-Driven Backflow.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2019
Historique:
entrez: 30 11 2018
pubmed: 30 11 2018
medline: 14 6 2019
Statut: ppublish

Résumé

It is well known that the resolving power of capillary zone electrophoretic separations may be improved with an increase in the applied electric field strength and separation time. While large electric fields may be realized in short analysis channels commonly employed in microfluidic systems, this experimental design is not suitable for achieving long separation times. In this chapter, we describe the use of a steady and/or a periodic pressure-driven backflow to increase the separation time in short microchannels thereby enabling the analysis of closely related species on microchip devices. The reported backflow was realized in our assays using an on-chip pressure-generation capability that relied on the partial blockage of electroosmotic flow around a junction of two glass channel segments having different depths. Although the noted strategy led to additional band broadening in the system, the resolving power of our device was observed to substantially improve upon introduction of the reported steady/periodic pressure-driven backflow for analysis channels shallower than 5 μm.

Identifiants

pubmed: 30488397
doi: 10.1007/978-1-4939-8964-5_16
pmc: PMC6771266
mid: NIHMS1052265
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

239-249

Subventions

Organisme : NIA NIH HHS
ID : R15 AG045755
Pays : United States

Références

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pubmed: 20503204
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pubmed: 23092536
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pubmed: 6623076

Auteurs

Ling Xia (L)

Department of Applied Chemistry, Sun Yat-Sun University, Guangzhou, People's Republic of China.

Debashis Dutta (D)

Department of Chemistry, University of Wyoming, Laramie, WY, USA. ddutta@uwyo.edu.

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Classifications MeSH