A Novel Microfluidic Point-of-Care Biosensor System on Printed Circuit Board for Cytokine Detection

被引:36
|
作者
Evans, Daniel [1 ]
Papadimitriou, Konstantinos I. [1 ]
Vasilakis, Nikolaos [1 ]
Pantelidis, Panagiotis [2 ,3 ]
Kelleher, Peter [2 ,3 ]
Morgan, Hywel [1 ,4 ]
Prodromakis, Themistoklis [5 ]
机构
[1] Univ Southampton, Elect & Comp Sci, Nanoelect & Nanotechnol Res Grp, Southampton SO17 1BJ, Hants, England
[2] Imperial Coll London, Dept Med, Div Infect Dis, Ctr Immunol & Vaccinol, London SW10 9NH, England
[3] Imperial Coll NHS Trust, Charing Cross Hosp, North West London Pathol, Infect & Immun, London W6 8RF, England
[4] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, Hants, England
[5] Univ Southampton, Zepler Inst Photon & Nanoelect, Southampton SO17 1BJ, Hants, England
基金
英国工程与自然科学研究理事会;
关键词
cytokine detection; eELISA; lab-on-PCB; microfluidics; PCB biosensors; point-of-care diagnostics; PAPER-BASED DEVICE; INTERFERON-GAMMA; DIAGNOSTICS; TECHNOLOGIES; DISEASE; GOLD; AMPLIFICATION; IMMUNOASSAY; BIOMARKERS; PLATFORM;
D O I
10.3390/s18114011
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Point of Care (PoC) diagnostics have been the subject of considerable research over the last few decades driven by the pressure to detect diseases quickly and effectively and reduce healthcare costs. Herein, we demonstrate a novel, fully integrated, microfluidic amperometric enzyme-linked immunosorbent assay (ELISA) prototype using a commercial interferon gamma release assay (IGRA) as a model antibody binding system. Microfluidic assay chemistry was engineered to take place on Au-plated electrodes within an assay cell on a printed circuit board (PCB)-based biosensor system. The assay cell is linked to an electrochemical reporter cell comprising microfluidic architecture, Au working and counter electrodes and a Ag/AgCl reference electrode, all manufactured exclusively via standard commercial PCB fabrication processes. Assay chemistry has been optimised for microfluidic diffusion kinetics to function under continual flow. We characterised the electrode integrity of the developed platforms with reference to biological sampling and buffer composition and subsequently we demonstrated concentration-dependent measurements of H2O2 depletion as resolved by existing FDA-validated ELISA kits. Finally, we validated the assay technology in both buffer and serum and demonstrate limits of detection comparable to high-end commercial systems with the addition of full microfluidic assay architecture capable of returning diagnostic analyses in approximately eight minutes.
引用
收藏
页数:14
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