Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/11878
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dc.contributor.authorBoonkaew S.
dc.contributor.authorTeengam P.
dc.contributor.authorJampasa S.
dc.contributor.authorRengpipat S.
dc.contributor.authorSiangproh W.
dc.contributor.authorChailapakul O.
dc.date.accessioned2021-04-05T03:01:21Z-
dc.date.available2021-04-05T03:01:21Z-
dc.date.issued2020
dc.identifier.issn32654
dc.identifier.other2-s2.0-85088487300
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/11878-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85088487300&doi=10.1039%2fd0an00564a&partnerID=40&md5=b8536e6ccd9049db639e0db723defd96
dc.description.abstractFerritin, a blood cell protein containing iron, is a crucial biomarker that is used to estimate the risk assessment of iron deficiency anemia. For point-of-care analysis, a reliable, cost-effective, selective, sensitive, and portable tool is extremely necessary. In this study, a label-free electrochemical immunosensor for detecting ferritin using a paper-based analytical device (ePAD) was created. The device pattern was custom designed onto filter paper to successfully fabricate a deliverable immunosensor. Graphene oxide was first modified onto the working electrode using an inkjet printing technique. An activation step of the electrode surface was then performed using standard 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)/N-hydroxysulfosuccinimide (sulfo-NHS) chemistry. Anti-ferritin antibodies were covalently immobilized onto the amine-reactive ester surface. The amount of ferritin was monitored by observing the electrochemical signal of the selected redox couple by differential pulse voltammetry (DPV). In the presence of ferritin, the sensor showed a considerable decrease in electrochemical response in a concentration-dependent manner. In contrast, there was no observable change in current response detected in the absence of ferritin. The current response provided a good correlation with ferritin concentrations in the range of 1 to 1000 ng mL-1, and the limit of detection (3SD/slope) was found to be 0.19 ng mL-1. This fabricated immunosensor offered good selectivity, reproducibility, and long-term storage stability. In addition, this proposed immunosensor was successfully applied to detect ferritin in human serum with satisfactory results. The promising results suggested that this handmade paper-based immunosensor may be an alternative device for the diagnosis of iron deficiency anemia. © 2020 The Royal Society of Chemistry.
dc.subjectAnalytic equipment
dc.subjectBlood
dc.subjectCost benefit analysis
dc.subjectCost effectiveness
dc.subjectGraphene
dc.subjectImmunosensors
dc.subjectInk jet printing
dc.subjectIron
dc.subjectPaper
dc.subjectRisk assessment
dc.subjectRisk perception
dc.subjectVoltammetry
dc.subjectConcentration-dependent manners
dc.subjectDifferential pulse voltammetry
dc.subjectElectrochemical immunosensors
dc.subjectElectrochemical response
dc.subjectElectrochemical signals
dc.subjectLong-term storage stability
dc.subjectPaper-based analytical devices
dc.subjectSensitive detection
dc.subjectElectrodes
dc.titleCost-effective paper-based electrochemical immunosensor using a label-free assay for sensitive detection of ferritin
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationAnalyst. Vol 145, No.14 (2020), p.5019-5026
dc.identifier.doi10.1039/d0an00564a
Appears in Collections:Scopus 1983-2021

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