2005
DOI: 10.1373/clinchem.2005.054882
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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

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Cited by 30 publications
(27 citation statements)
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“…Just as in the initial biomarker validation phases, our LOC studies also document measurable signal differences in protein fingerprint patterns of these 2 patient groups. Bead-based immunoassay systems display strong analytical performance characteristics (typical intraassay variance of 4%-8% and interassay variance of 6%-10%) (26,27,31 ). Correlation studies completed with FDAapproved instruments for serum CRP yield R 2 values of 0.98.…”
Section: Discussionmentioning
confidence: 99%
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“…Just as in the initial biomarker validation phases, our LOC studies also document measurable signal differences in protein fingerprint patterns of these 2 patient groups. Bead-based immunoassay systems display strong analytical performance characteristics (typical intraassay variance of 4%-8% and interassay variance of 6%-10%) (26,27,31 ). Correlation studies completed with FDAapproved instruments for serum CRP yield R 2 values of 0.98.…”
Section: Discussionmentioning
confidence: 99%
“…Design, fabrication, and testing methods for LOC structures have been described in detail in previous reports (23,24,26,27,30,31 ). New modifications to procedures and methods for multiplexed AMI diagnosis are described in the Supplemental Data section (see Lab-on-aChip (LOC) Multiplexed Test in Supplemental Materials in the Data Supplement that accompanies the online version of this article at http://www.clinchem.org/content/ vol55/issue8]).…”
Section: Loc Multiplexed Testmentioning
confidence: 99%
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“…to this end, we have combined the bead-based and membrane-based P-BnC platforms to provide a dual-function CrP and white blood cell cardiac risk measurement tool, thus making the P-BnC the only PoC system amenable for the combined measurement of both cellular and proteomic biomarkers of cardiac risk. [29][30][31] our initial cross-sectional biomarker discovery study also demonstrated the potential utility for ctni as a salivary biomarker of aMi despite its low concentration in this biological fluid. it must be noted that an essential prerequisite for the successful implementation of this biomarker in PoC practice, whether in needle-prick-derived whole blood or saliva, depends on the availability of an ultra-sensitive method for its measurement.…”
Section: Bio-nanochips For Cvd Diagnosticsmentioning
confidence: 84%
“…Whole saliva derives additional constituents from serum, gingival crevicular fluid and oral mucosal transudate, making it appealing as a potential diagnostic fluid reflective of circulating levels in blood. 1 Several studies report systemic biomarkers appearing in saliva including electrolytes, 2, 3 blood products, 4 enzymes and tissue destruction molecules, 59 inflammatory markers, 1016 as well as proteins putatively associated with deadly diseases. 1721 However, the clinical utility of salivary diagnostics for the assessment of systemic disease remains elusive.…”
mentioning
confidence: 99%