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Clinical Chemistry 51: 2391-2395, 2005; 10.1373/clinchem.2005.054882
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(Clinical Chemistry. 2005;51:2391-2395.)
© 2005 American Association for Clinical Chemistry, Inc.


Technical Briefs

Toward the Development of a Lab-on-a-Chip Dual-Function Leukocyte and C-Reactive Protein Analysis Method for the Assessment of Inflammation and Cardiac Risk

Nicolaos Christodoulides1, Pierre N. Floriano1, Shelley A. Acosta1, Karri L. Michael Ballard1, Shannon E. Weigum1, Sanghamitra Mohanty1, Priya Dharshan1, Dwight Romanovicz1 and John T. McDevitt1,2,3,a

1 Department of Chemistry & Biochemistry, and the2 Center for Nano and Molecular Science and Technology,3 Texas Materials Institute, The University of Texas at Austin, Austin, TX

aaddress correspondence to this author at: Department of Chemistry & Biochemistry, Texas Materials Institute, The University of Texas at Austin, Austin, TX 78735; fax 512-232-7052, e-mail mcdevitt@mail.utexas.edu

The first 300 words of the full text of this article appear below.

Inflammation has been identified as the underlying cause of atherosclerosis, a condition associated with the deposition of lipids in the lining of arteries, which progressively leads to acute myocardial infraction (AMI) or heart attack. Serum concentrations of markers of inflammation, including C-reactive protein (CRP), and the leukocyte count are powerful predictors for the development of coronary heart disease (1)(2)(3)(4)(5)(6)(7). In addition, AMI patients with increased CRP concentrations or leukocyte counts are at higher risk of mortality and recurrent AMI (8)(9)(10)(11)(12). The combination of these 2 biomarkers provides additive and powerful diagnostic information. In fact, people with both high leukocyte counts and high CRP concentrations exhibit a 7-fold higher risk for heart disease (7).

Although tests targeting CRP concentrations and leukocyte counts are widely available in clinical settings, they are performed separately on different instruments. Consequently, these tests require large sample volumes, additional sample preparation steps, and longer assay times. In addition, the clinical instruments and methodologies currently used to perform these tests are not suitable for point-of-care testing, such as in a doctor’s office and in the (more relevant to a heart attack setting) emergency room or ambulance. Clearly, the diagnostic and prognostic value of these biomarkers would be increased if these 2 tests could be performed concurrently on the same instrument, in a convenient, accurate, and highly accessible manner.

Previously we described studies of the design, fabrication, and testing of lab-on-a-chip (LOC) structures composed of chemically sensitized beads that are populated into etched silicon wafers with integrated fluid-handling and optical detection capabilities (13)(14)(15)(16)(17)(18)(19). These miniaturized systems have been used . . . [Full Text of this Article]




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Home page
Clin. Chem.Home page
Edited on behalf of the National Institute of Biom, C. P. Price, and L. J. Kricka
Improving Healthcare Accessibility through Point-of-Care Technologies
Clin. Chem., September 1, 2007; 53(9): 1665 - 1675.
[Abstract] [Full Text] [PDF]




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