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Biochemical-immunological hybrid biosensor based on two-dimensional chromatography for on-site sepsis diagnosis.
Kim, Seung-Wan; Cho, Il-Hoon; Lim, Guei-Sam; Park, Gi-Na; Paek, Se-Hwan.
Affiliation
  • Kim SW; Department of Bio-Microsystem Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, South Korea.
  • Cho IH; Department of Biomedical Laboratory Science, College of Health Science, Eulji University, 553 Sanseong-daero, Sujeong-gu, Seongnam, Kyonggi-do 13135, South Korea.
  • Lim GS; Department of Bio-Microsystem Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, South Korea; Healthcare Group, Emerging Technology Lab., LG Electronics Advanced Research Institute, 38 Baumoe-ro, Seocho-gu, Seoul 06763, South Korea.
  • Park GN; Department of Bio-Microsystem Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, South Korea.
  • Paek SH; Department of Bio-Microsystem Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, South Korea; Department of Biotechnology and Bioinformatics, Korea University, 2511 Sejong-ro, Sejong 30019, South Korea. Electronic address: shpaek@korea.ac.kr.
Biosens Bioelectron ; 98: 7-14, 2017 Dec 15.
Article in En | MEDLINE | ID: mdl-28646721
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 (R2 > 0.95) with the reference systems for the target markers.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcitonin / Immunoassay / Biosensing Techniques / Sepsis Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Biosens Bioelectron Journal subject: BIOTECNOLOGIA Year: 2017 Document type: Article Affiliation country: Corea del Sur

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcitonin / Immunoassay / Biosensing Techniques / Sepsis Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Biosens Bioelectron Journal subject: BIOTECNOLOGIA Year: 2017 Document type: Article Affiliation country: Corea del Sur