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A novel electrochemical strategy for NT-proBNP detection using IMFET for monitoring heart failure by saliva analysis

Authors :
EU's Horizon 2020 research and innovation program
#NODATA#
0000-0002-8956-451X
0000-0002-6839-3002
0000-0003-3706-4975
Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]
Ben Halima, Hamdi
Bellagambi, Francesca G
Hangouët, Marie
Alcacer, Albert
Pfeiffer, Norman
Heuberger, Albert
Zine, Nadia
Bausells, Joan
Elaissari, Abdelhamid
Errachid, Abdelhamid
EU's Horizon 2020 research and innovation program
#NODATA#
0000-0002-8956-451X
0000-0002-6839-3002
0000-0003-3706-4975
Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]
Ben Halima, Hamdi
Bellagambi, Francesca G
Hangouët, Marie
Alcacer, Albert
Pfeiffer, Norman
Heuberger, Albert
Zine, Nadia
Bausells, Joan
Elaissari, Abdelhamid
Errachid, Abdelhamid
Publication Year :
2023

Abstract

Heart failure (HF) is a chronic cardiovascular disease that represents main cause of mortality worldwide, particularly for elderly. N-terminal pro-brain natriuretic peptide (NT-proBNP) was identified as the gold standard biomarker for HF diagnosis and therapy monitoring. Presently, saliva analysis represents an emerging and powerful tool for clinical applications and electrochemical immunosensors have shown their potential in Healthcare applications as selective and reliable systems for detecting clinical biomarkers. This work presents the detection of NT-proBNP in saliva samples by an immunologically modified Field effect Transistor (IMFET). TESUD ((11-triethoxysilyl) undecanal) was used as cross-linker to immobilise anti-NT-proBNP antibody onto the device. Our IMFET that was then tested in different matrices (e.g. phosphate buffered saline (PBS), artificial saliva and human saliva) using electrochemical impedance spectroscopy (EIS), and it resulted selective to NT-proBNP with good sensitivity (detection limit of 0.02 pg/mL) and a wide linear range (0.02-1 pg/mL and 0.5-20 pg/mL). Finally, NT-proBNP concentration in ten saliva samples was determined by performing the standard addition method. An enzyme-linked immunosorbent assay was used for confirming IMFET results, highlighting both IMFET accuracy (analyte recovery of 99 ± 8%) and precision (coefficient of variation always <10%), and supporting the suitability of the device for determining salivary NT-proBNP.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1442723605
Document Type :
Electronic Resource