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Dual-mode ion-selective electrodes and distance-based microfluidic device for detection of multiple urinary electrolytes

dc.contributor.authorPhoonsawat, Kamonchanok
dc.contributor.authorOzer, Tugba
dc.contributor.authorDungchai, Wijitar
dc.contributor.authorHenry, Charles S.
dc.date.accessioned2026-06-27T14:43:01Z
dc.date.issued2022
dc.description.abstractHere, we developed a microfluidic paper device by combining ion-selective electrodes (ISE) and a distance-based paper device (dPAD) for simultaneous potentiometric and colorimetric detection of urine electrolytes including K+, Na+ and Cl-. The working and reference electrode zones were coated with polystyrene as a non-ionic polymer to improve hydrophobic properties on the paper surface for fabrication of K+-ISE and Na+-ISE. The layer of polymer coating was optimized to enhance the sensitivity of the ISEs. Under optimized conditions, the electrode surfaces were modified with carbon black to improve the electrochemical characteristics of the ISEs. The ISEs showed good performance with sensitivities of 54.14 +/- 3.94 mV per decade and 55.08 +/- 1.15 mV per decade for K+ and Na+ within the linear concentration range 0.100 mM-100 mM K+ and 5 mM-1 M Na+, respectively. The limits of detection (LOD) were 0.05 mM and 1.36 mM for K+ and Na+, respectively. The linear working range of Cl- was 0.50 to 50 mM and the LOD and limit of quantification (LOQ) were found to be 0.16 +/- 0.05 mM (3SD) and 0.53 +/- 0.05 mM (10SD), respectively. The dual-mode ISE-dPAD was validated in human urine and recoveries were obtained as 90-108%, 94-105%, and 90-96% for K+, Na+, and Cl-, respectively, showing successful application of the developed device in a complex matrix. The ISE-dPAD has advantages including low-cost ($ 0.33 per test), eco-friendly, portability, simple operation, the need of low sample volume (100 mu L), and simultaneous analysis on a single device.en
dc.description.sponsorshipPetchra Pra Jom Klao Ph.D. Research Scholarship, Innovation and Partnerships Office, King Mongkut's University of Technology Thonburi, Thailand
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK), Turkey [120N615]
dc.description.sponsorshipColorado State University, USA
dc.description.urihttps://doi.org/10.1039/d2an01220k
dc.identifier.doi10.1039/d2an01220k
dc.identifier.eissn1364-5528
dc.identifier.endpage4524
dc.identifier.issn0003-2654
dc.identifier.issue20
dc.identifier.pubmed36074753
dc.identifier.startpage4517
dc.identifier.urihttps://hdl.handle.net/20.500.14981/63871
dc.identifier.volume147
dc.identifier.wos000851159500001
dc.language.isoeng
dc.publisherROYAL SOC CHEMISTRY
dc.relation.ispartofANALYST
dc.subjectPOTASSIUM INTAKE
dc.subjectSODIUM
dc.subjectCHLORIDE
dc.subjectHYPERTENSION
dc.subjectTIME
dc.subjectK+
dc.subjectChemistry
dc.titleDual-mode ion-selective electrodes and distance-based microfluidic device for detection of multiple urinary electrolytes
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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