Detection of the Inflammation Biomarker C-Reactive Protein in Serum Samples: Towards an Optimal Biosensor Formula

The development of an electrochemical immunosensor for the biomarker, C-reactive protein (CRP), is reported in this work. CRP has been used to assess inflammation and is also used in a multi-biomarker system as a predictive biomarker for cardiovascular disease risk. A gold-based working electrode s...

Full description

Bibliographic Details
Main Authors: Wellington M. Fakanya, Ibtisam E. Tothill
Format: Article
Language:English
Published: MDPI AG 2014-10-01
Series:Biosensors
Subjects:
CRP
Online Access:http://www.mdpi.com/2079-6374/4/4/340
id doaj-cfa20a9c73a849809503796b3a236763
record_format Article
spelling doaj-cfa20a9c73a849809503796b3a2367632020-11-24T23:35:33ZengMDPI AGBiosensors2079-63742014-10-014434035710.3390/bios4040340bios4040340Detection of the Inflammation Biomarker C-Reactive Protein in Serum Samples: Towards an Optimal Biosensor FormulaWellington M. Fakanya0Ibtisam E. Tothill1Centre of Biomedical Engineering, Cranfield University, Cranfield, Bedfordshire, MK43 0AL, UKCentre of Biomedical Engineering, Cranfield University, Cranfield, Bedfordshire, MK43 0AL, UKThe development of an electrochemical immunosensor for the biomarker, C-reactive protein (CRP), is reported in this work. CRP has been used to assess inflammation and is also used in a multi-biomarker system as a predictive biomarker for cardiovascular disease risk. A gold-based working electrode sensor was developed, and the types of electrode printing inks and ink curing techniques were then optimized. The electrodes with the best performance parameters were then employed for the construction of an immunosensor for CRP by immobilizing anti-human CRP antibody on the working electrode surface. A sandwich enzyme-linked immunosorbent assay (ELISA) was then constructed after sample addition by using anti-human CRP antibody labelled with horseradish peroxidase (HRP). The signal was generated by the addition of a mediator/substrate system comprised of 3,3,5',5'-Tetramethylbenzidine dihydrochloride (TMB) and hydrogen peroxide (H2O2). Measurements were conducted using chronoamperometry at −200 mV against an integrated Ag/AgCl reference electrode. A CRP limit of detection (LOD) of 2.2 ng·mL−1 was achieved in spiked serum samples, and performance agreement was obtained with reference to a commercial ELISA kit. The developed CRP immunosensor was able to detect a diagnostically relevant range of the biomarker in serum without the need for signal amplification using nanoparticles, paving the way for future development on a cardiac panel electrochemical point-of-care diagnostic device.http://www.mdpi.com/2079-6374/4/4/340electrochemical immunosensorC-reactive proteinCRPbiomarkerserum
collection DOAJ
language English
format Article
sources DOAJ
author Wellington M. Fakanya
Ibtisam E. Tothill
spellingShingle Wellington M. Fakanya
Ibtisam E. Tothill
Detection of the Inflammation Biomarker C-Reactive Protein in Serum Samples: Towards an Optimal Biosensor Formula
Biosensors
electrochemical immunosensor
C-reactive protein
CRP
biomarker
serum
author_facet Wellington M. Fakanya
Ibtisam E. Tothill
author_sort Wellington M. Fakanya
title Detection of the Inflammation Biomarker C-Reactive Protein in Serum Samples: Towards an Optimal Biosensor Formula
title_short Detection of the Inflammation Biomarker C-Reactive Protein in Serum Samples: Towards an Optimal Biosensor Formula
title_full Detection of the Inflammation Biomarker C-Reactive Protein in Serum Samples: Towards an Optimal Biosensor Formula
title_fullStr Detection of the Inflammation Biomarker C-Reactive Protein in Serum Samples: Towards an Optimal Biosensor Formula
title_full_unstemmed Detection of the Inflammation Biomarker C-Reactive Protein in Serum Samples: Towards an Optimal Biosensor Formula
title_sort detection of the inflammation biomarker c-reactive protein in serum samples: towards an optimal biosensor formula
publisher MDPI AG
series Biosensors
issn 2079-6374
publishDate 2014-10-01
description The development of an electrochemical immunosensor for the biomarker, C-reactive protein (CRP), is reported in this work. CRP has been used to assess inflammation and is also used in a multi-biomarker system as a predictive biomarker for cardiovascular disease risk. A gold-based working electrode sensor was developed, and the types of electrode printing inks and ink curing techniques were then optimized. The electrodes with the best performance parameters were then employed for the construction of an immunosensor for CRP by immobilizing anti-human CRP antibody on the working electrode surface. A sandwich enzyme-linked immunosorbent assay (ELISA) was then constructed after sample addition by using anti-human CRP antibody labelled with horseradish peroxidase (HRP). The signal was generated by the addition of a mediator/substrate system comprised of 3,3,5',5'-Tetramethylbenzidine dihydrochloride (TMB) and hydrogen peroxide (H2O2). Measurements were conducted using chronoamperometry at −200 mV against an integrated Ag/AgCl reference electrode. A CRP limit of detection (LOD) of 2.2 ng·mL−1 was achieved in spiked serum samples, and performance agreement was obtained with reference to a commercial ELISA kit. The developed CRP immunosensor was able to detect a diagnostically relevant range of the biomarker in serum without the need for signal amplification using nanoparticles, paving the way for future development on a cardiac panel electrochemical point-of-care diagnostic device.
topic electrochemical immunosensor
C-reactive protein
CRP
biomarker
serum
url http://www.mdpi.com/2079-6374/4/4/340
work_keys_str_mv AT wellingtonmfakanya detectionoftheinflammationbiomarkercreactiveproteininserumsamplestowardsanoptimalbiosensorformula
AT ibtisametothill detectionoftheinflammationbiomarkercreactiveproteininserumsamplestowardsanoptimalbiosensorformula
_version_ 1725525663812681728