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Biochemical-immunological hybrid biosensor based on two-dimensional chromatography for on-site sepsis diagnosis

Authors
Kim, Seung-WanCho, Il-HoonLim, Guei-SamPark, Gi-NaPaek, Se-Hwan
Issue Date
15-12월-2017
Publisher
ELSEVIER ADVANCED TECHNOLOGY
Keywords
Heterogeneous analytes; Multiplexed biosensing; Two-dimensional chromatography; Smartphone detector; Rapid sepsis diagnosis
Citation
BIOSENSORS & BIOELECTRONICS, v.98, pp.7 - 14
Indexed
SCIE
SCOPUS
Journal Title
BIOSENSORS & BIOELECTRONICS
Volume
98
Start Page
7
End Page
14
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/81173
DOI
10.1016/j.bios.2017.06.032
ISSN
0956-5663
Abstract
A hybrid-biosensor system that can simultaneously fulfill the immunoassay for protein markers (e.g., C-reactive protein (CRP) and procalcitonin (PCT)) and the enzyme assay for metabolic substances (e.g., lactate) in the same sepsis-based sample has been devised. Such a challenge was pursued through the installation of an enzyme-reaction zone on the signal pad of the typical immuno-strip for the rapid two-dimensional (2-D)-chromatography test. To minimize the mutual interference in the hybrid assays, a pre-determined membrane site was etched in a pattern and mounted with a biochemical-reaction pad, thereby allowing a loaded sample to enter and then stay in the pad for a colored-signal production over the course of an immunoassay. By employing such a constructed system, a serum sample was analyzed according to the vertical direction flowing along the strip, which supplied lactate to the biochemical-reaction zone and then protein markers to the immunological-binding area that was pre-coated with capture antibodies. Thereafter, the enzyme-signal tracers for the immunoassay and the substrate solution were sequentially furnished using a horizontal path for the tracing of the immune complexes that were formed with CRP or PCT. The color signal that was produced from each assay was detected at a pre-determined time and quantified on a smartphone-based detector. Under the optimal conditions, the dynamic ranges for the analytes covered the respective clinical ranges, and the total coefficient of variation was between 8.6% and 13.3%. The hybrid biosensor further showed a high correlation (R-2 > 0.95) with the reference systems for the target markers.
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