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...
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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 |
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