An Assay System for Point-of-Care Diagnosis of Tuberculosis using Commercially Manufactured PCB Technology

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作者
Daniel Evans
Konstantinos I. Papadimitriou
Louise Greathead
Nikolaos Vasilakis
Panagiotis Pantelidis
Peter Kelleher
Hywel Morgan
Themistoklis Prodromakis
机构
[1] University of Southampton,Nanoelectronics & Nanotechnology Research Group, School of Electronics and Computer Science
[2] Imperial College London,Centre for Immunology and Vaccinology, Division of Infectious Diseases, Department of Medicine
[3] Infection and Immunity,undefined
[4] Imperial College NHS Trust,undefined
[5] Charing Cross Hospital,undefined
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Rapid advances in clinical technologies, detection sensitivity and analytical throughput have delivered a significant expansion in our knowledge of prognostic and diagnostic biomarkers in many common infectious diseases, such as Tuberculosis (TB). During the last decade, a significant number of approaches to TB diagnosis have been attempted at Point-of-Care (PoC), exploiting a large variation of techniques and materials. In this work, we describe an electronics-based Enzyme-Linked ImmunoSorbent Assay (eELISA), using a Lab-on-a-Printed Circuit Board (LoPCB) approach, for TB diagnosis based on cytokine detection. The test relies upon an electrochemical (amperometric) assay, comprising a high-precision bioinstrumentation board and amperometric sensors, produced exclusively using standard PCB manufacturing processes. Electrochemical detection uses standard Au and Ag electrodes together with a bespoke, low-power, multichannel, portable data-acquisition system. We demonstrate high-performance assay chemistry performed at microfluidic volumes on Au pads directly at the PCB surface with improved limit of detection (~10 pg/mL) over standard colorimetric ELISA methods. The assay has also been implemented in plasma, showing the utility of the system for medical applications. This work is a significant step towards the development of a low-cost, portable, high-precision diagnostic and monitoring technology, which once combined with appropriate PCB-based microfluidic networks will provide complete LoPCB platforms.
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