DocumentCode
3166338
Title
Chip-based clinical assays: towards analysis of physiological samples
Author
Ceriotti, L. ; Shibata, T. ; Linder, V. ; Thormann, W. ; Sigrist, H. ; de Rooij, N.F. ; Verpoorter, E.
Author_Institution
Inst. of Microtechnology, Neuchatel Univ., Switzerland
fYear
2002
fDate
6-8 Nov. 2002
Firstpage
272
Lastpage
273
Abstract
There are a number of challenges, both engineering and chemical, which still need to be overcome before the use of so-called miniaturized total chemical analysis systems, or /spl mu/TAS, becomes well established in the clinical domain. These are related to the complex nature of physiological media, which are inherently incompatible with microchannels having cross-sectional dimensions on the order of micrometers. The high surface-to-volume ratios of microfluidic devices are the primary concern, since biomolecules are prone to increased adsorption in these systems. Special consideration must therefore be given to analysis of protein-containing matrices in microflow systems, and analysis conditions adjusted to the type of analyte and chip substrate in question.
Keywords
adsorption; biosensors; capillarity; chemical analysis; electrophoresis; microfluidics; osmosis; proteins; /spl mu/TAS; adsorption; biomolecular analytes; capillary electrophoresis; chip-based clinical assays; electro-osmosis pumping; lipoprotein; microchannels; microflow systems; microfluidic devices; miniaturized total chemical analysis systems; physiological fluids; pulseless solution flows; surface-to-volume ratio; Biomedical monitoring; Chemical analysis; Chemical engineering; Chemical technology; Chemistry; Hardware design languages; Immune system; Microchannel; Microfluidics; Proteins;
fLanguage
English
Publisher
ieee
Conference_Titel
Microprocesses and Nanotechnology Conference, 2002. Digest of Papers. Microprocesses and Nanotechnology 2002. 2002 International
Conference_Location
Tokyo, Japan
Print_ISBN
4-89114-031-3
Type
conf
DOI
10.1109/IMNC.2002.1178648
Filename
1178648
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