Paper-based potentiometric sensing of free bilirubin in blood serum.


Journal

Biosensors & bioelectronics
ISSN: 1873-4235
Titre abrégé: Biosens Bioelectron
Pays: England
ID NLM: 9001289

Informations de publication

Date de publication:
01 Feb 2019
Historique:
received: 12 08 2018
revised: 04 10 2018
accepted: 25 10 2018
pubmed: 6 11 2018
medline: 16 4 2019
entrez: 6 11 2018
Statut: ppublish

Résumé

Bilirubin is predominantly formed in the liver as a result of breakdown of hemoglobin. Knowing the concentration of bilirubin in serum is important in evaluating the health of the liver, and for the diagnosis of hyperbilirubinemia (a condition that afflicts approximately 60% of full-term and 80% of pre-term newborns). This paper describes the design and fabrication of a potentiometric sensor for the determination of free bilirubin in serum. The sensor has a polymeric ion-selective membrane, and selectively measures free ionic bilirubin ("unbound" bilirubin - i.e., bilirubin not complexed to albumin or other complexing agents), in the presence of other anions - chloride, phosphate, pyruvate, deoxycholate, and lactate - also present in serum. The linear response range of the sensor (1.0 mM to 0.10 μM bilirubin, measured in a sodium phosphate buffer with pH 8.6) covers the clinically-relevant concentration of bilirubin in serum (5-500 μM). Free bilirubin could be detected in human blood serum with this potentiometric sensor. The components of the potentiometric bilirubin sensor were embedded in a paper-based device to provide a sensor that is disposable and easy to use, and thus is suitable for applications at the point-of-care. The paper-based potentiometric bilirubin sensor exhibited a response range of 5.0-0.10 mM (sufficient to cover the clinically-relevant concentration of bilirubin in serum). Only 15 μL of sample is required for measurement of the concentration of free bilirubin, and the analysis can be performed in less than two minutes.

Identifiants

pubmed: 30396018
pii: S0956-5663(18)30872-8
doi: 10.1016/j.bios.2018.10.055
pii:
doi:

Substances chimiques

Bilirubin RFM9X3LJ49

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115-121

Informations de copyright

Copyright © 2018 Elsevier B.V. All rights reserved.

Auteurs

Jeffrey G Bell (JG)

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, MA 02138, United States.

Maral P S Mousavi (MPS)

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, MA 02138, United States.

Mohamed K Abd El-Rahman (MK)

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, MA 02138, United States; Department of Analytical Chemistry, Faculty of Pharmacy, Cairo University, Kasr-El Ani Street, Cairo 11562, Egypt.

Edward K W Tan (EKW)

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, MA 02138, United States; Department of Engineering, University of Cambridge, Cambridge CB3 0FA, UK.

Shervanthi Homer-Vanniasinkam (S)

Leeds Vascular Institute, Leeds General Infirmary, Leeds, UK; Department of Mechanical Engineering and Division of Surgery, University College London, London, UK; Division of Surgery, University of Warwick, Coventry, UK.

George M Whitesides (GM)

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, MA 02138, United States; Kavli Institute for Bionano Inspired Science and Technology, School of Engineering and Applied Sciences, Harvard University, 29 Oxford Street, MA 02138, United States; Wyss Institute for Biologically Inspired Engineering, Harvard University, 60 Oxford Street, MA 02138, United States. Electronic address: gwhitesides@gmwgroup.harvard.edu.

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