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Capillary-based enzyme-linked immunosorbent assay for highly sensitive detection of thrombin-cleaved osteopontin in plasma
Authors:Shun-ichi Funano  Terence G. Henares  Mie Kurata  Kenji Sueyoshi  Tatsuro Endo  Hideaki Hisamoto
Affiliation:1. Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Osaka 599-8531, Japan;2. Department of Pathogenomics, Graduate School of Medicine, Ehime University, Ehime 791-0295, Japan;3. Department of Cardiology, Thorax Center of Erasmus Medical Center, 3000 CA Rotterdam, The Netherlands
Abstract:In this study, a highly sensitive capillary-based enzyme-linked immunosorbent assay (ELISA) has been developed for the analysis of picomolar levels of thrombin-cleaved osteopontin (trOPN), a potential biomarker for ischemic stroke, in human plasma. Using a square capillary coated with 8.5 μg/ml anti-human trOPN capture antibody for ELISA, the linear range obtained was 2 to 16 pM trOPN antigen. This concentration range was in the detection window of trOPN antigen in plasma samples. Compared with the conventional microplate-based ELISA, the current capillary technique significantly reduced the amounts of reagent from milliliter to microliter, reduced the analysis time from 8 to 3 h, and had a better sensitivity and detection limit performance from approximately 50 pM down to 2 pM of trOPN antigen. These results indicate that this capillary-based immunoassay is a potential tool for biomarker detection and may be useful in clinical trials and medical diagnostic applications.
Keywords:Square glass capillary   Enzyme-linked immunosorbent assay (ELISA)   Thrombin-cleaved osteopontin (trOPN)
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