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Title: | An automated fast-flow/delayed paper-based platform for the simultaneous electrochemical detection of hepatitis B virus and hepatitis C virus core antigen |
Authors: | Boonkaew S. Yakoh A. Chuaypen N. Tangkijvanich P. Rengpipat S. Siangproh W. Chailapakul O. |
Keywords: | Antigens Channel flow Chemical detection Microfluidics Paper Viruses ELectrochemical detection Electrochemicals Hepatitis B surface antigen Hepatitis B virus Hepatitis C virus Hepatitis C virus core antigen Microfluidic paper-based analytical device Multi-step Paper-based analytical devices Point-of-care testing Analytic equipment biological marker buffer graphene hepatitis B core antigen hepatitis B surface antigen oxidoreductase potassium chloride hepatitis B surface antigen hepatitis C antigen Article blood sampling chronoamperometry cyclic voltammetry electrochemical analysis electrochemical detection electron transport hepatitis B Hepatitis B virus hepatitis C Hepatitis C virus human impedance spectroscopy microfluidics point of care testing genetic procedures Hepacivirus hepatitis B Hepatitis B virus Biosensing Techniques Electrochemical Techniques Hepacivirus Hepatitis B Hepatitis B Surface Antigens Hepatitis B virus Hepatitis C Antigens Humans |
Issue Date: | 2021 |
Abstract: | Electrochemical paper-based analytical devices (ePADs) are useful analytical devices that serve as point-of-care testing (POCT) devices for various clinical biomarkers in view of their simplicity, portability, and low-cost format. However, multistep reagent manipulation usually restricts the performance of the device for end users. Herein, we developed a sequential ePAD for sequential immunosensing fluid delivery by integrating dual flow behaviors (fast-flow/delayed) within a single paper platform for the simultaneous detection of hepatitis B surface antigen (HBsAg) and hepatitis C core antigen (HCVcAg). In the present work, a fast-flow channel was used for the automated washing of unbound antigens, while a delayed channel was created to store a redox reagent for further electrochemical analysis with a single buffer loading (the analysis time can be completed within 500 s). Hence, the undesirable complex procedure of multi-step reagent manipulation is scarcely needed by the user. The detection limit of the proposed ePAD was as low as 18.2 pg mL−1 for HBsAg and 1.19 pg mL−1 for HCVcAg. In addition, this proposed ePAD was also proven to be effective in real clinical sera from patients to verify its biological applicability. The ePAD sensor shows high promise as an easy-to-use, portable, and extendable sensor for other multiplex biological assays. © 2021 Elsevier B.V. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/17399 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85112754391&doi=10.1016%2fj.bios.2021.113543&partnerID=40&md5=34deba761eacc8172587bb051c8acb34 |
ISSN: | 9565663 |
Appears in Collections: | Scopus 1983-2021 |
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