Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13543
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dc.contributor.authorPreechakasedkit P.
dc.contributor.authorSiangproh W.
dc.contributor.authorKhongchareonporn N.
dc.contributor.authorNgamrojanavanich N.
dc.contributor.authorChailapakul O.
dc.date.accessioned2021-04-05T03:24:35Z-
dc.date.available2021-04-05T03:24:35Z-
dc.date.issued2018
dc.identifier.issn9565663
dc.identifier.other2-s2.0-85032704512
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13543-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85032704512&doi=10.1016%2fj.bios.2017.10.051&partnerID=40&md5=c512cd71e651730e917c3afed2b9791b
dc.description.abstractIn this study, a novel wax-printed paper-based lateral flow device has been developed as an alternative approach for an automated and one-step enzyme-linked immunosorbent assay (ELISA). The design pattern consisted of a non-delayed channel, a wax-delayed channel, a test zone and a control zone. This system was easily fabricated on a nitrocellulose membrane using a wax-printing method and then baked in an oven at 100 °C for 1 min. The four barriers of the wax-delayed channel could delay the flow time for 11 s compared to the flow time of the non-delayed channel. To use the device under optimal conditions, alpha-fetoprotein (AFP) was detected at a limit of detection of 1 ng mL−1 and assessed with the naked eye within 10 min. A colorimetric intensity was also measured using a smart phone and computer software at a linear range of 0.1–100 ng mL−1 with a good correlation. Furthermore, the proposed device was successfully applied to detect AFP in human serum. Therefore, the wax-printing demonstrates a user-friendly, easy and quick method for the fabrication of the device, which could be used as a one-step, portable, disposable, low-cost, simple, instrument-free and point-of-care device for the automated ELISA. © 2017
dc.subjectAutomation
dc.subjectEnzymes
dc.subjectSmartphones
dc.subjectAlpha fetoprotein
dc.subjectEnzyme linked immunosorbent assay
dc.subjectLateral Flow
dc.subjectPoint-of-care testing
dc.subjectWax printings
dc.subjectBioassay
dc.subjectalpha fetoprotein
dc.subjectpyroxylin
dc.subjectalpha fetoprotein
dc.subjectwax
dc.subjectArticle
dc.subjectbioprinting
dc.subjectcolorimetry
dc.subjectconcentration (parameters)
dc.subjectcontrolled study
dc.subjectenzyme linked immunosorbent assay
dc.subjecthuman
dc.subjectlimit of detection
dc.subjectmeasurement precision
dc.subjectnanofabrication
dc.subjectpoint of care testing
dc.subjectwax printed paper based lateral flow device
dc.subjectchemistry
dc.subjectdevices
dc.subjecteconomics
dc.subjectenzyme linked immunosorbent assay
dc.subjectequipment design
dc.subjectevaluation study
dc.subjectgenetic procedures
dc.subjectmicrofluidic analysis
dc.subjectpaper
dc.subjectsmartphone
dc.subjectalpha-Fetoproteins
dc.subjectBiosensing Techniques
dc.subjectCollodion
dc.subjectColorimetry
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subjectEquipment Design
dc.subjectHumans
dc.subjectLimit of Detection
dc.subjectMicrofluidic Analytical Techniques
dc.subjectPaper
dc.subjectPoint-of-Care Testing
dc.subjectSmartphone
dc.subjectWaxes
dc.titleDevelopment of an automated wax-printed paper-based lateral flow device for alpha-fetoprotein enzyme-linked immunosorbent assay
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationBiosensors and Bioelectronics. Vol 102, (2018), p.27-32
dc.identifier.doi10.1016/j.bios.2017.10.051
Appears in Collections:Scopus 1983-2021

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