Cargando…

Microfluidic Impedance Biosensor Chips Using Sensing Layers Based on DNA-Based Self-Assembled Monolayers for Label-Free Detection of Proteins

A microfluidic chip for electrochemical impedance spectroscopy (EIS) is presented as bio-sensor for label-free detection of proteins by using the example of cardiac troponin I. Troponin I is one of the most specific diagnostic serum biomarkers for myocardial infarction. The microfluidic impedance bi...

Descripción completa

Detalles Bibliográficos
Autores principales: Alsabbagh, Khaled, Hornung, Tim, Voigt, Achim, Sadir, Sahba, Rajabi, Taleieh, Länge, Kerstin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001378/
https://www.ncbi.nlm.nih.gov/pubmed/33805676
http://dx.doi.org/10.3390/bios11030080
_version_ 1783671215851831296
author Alsabbagh, Khaled
Hornung, Tim
Voigt, Achim
Sadir, Sahba
Rajabi, Taleieh
Länge, Kerstin
author_facet Alsabbagh, Khaled
Hornung, Tim
Voigt, Achim
Sadir, Sahba
Rajabi, Taleieh
Länge, Kerstin
author_sort Alsabbagh, Khaled
collection PubMed
description A microfluidic chip for electrochemical impedance spectroscopy (EIS) is presented as bio-sensor for label-free detection of proteins by using the example of cardiac troponin I. Troponin I is one of the most specific diagnostic serum biomarkers for myocardial infarction. The microfluidic impedance biosensor chip presented here consists of a microscope glass slide serving as base plate, sputtered electrodes, and a polydimethylsiloxane (PDMS) microchannel. Electrode functionalization protocols were developed considering a possible charge transfer through the sensing layer, in addition to analyte-specific binding by corresponding antibodies and reduction of nonspecific protein adsorption to prevent false-positive signals. Reagents tested for self-assembled monolayers (SAMs) on gold electrodes included thiolated hydrocarbons and thiolated oligonucleotides, where SAMs based on the latter showed a better performance. The corresponding antibody was covalently coupled on the SAM using carbodiimide chemistry. Sampling and measurement took only a few minutes. Application of a human serum albumin (HSA) sample, 1000 ng/mL, led to negligible impedance changes, while application of a troponin I sample, 1 ng/mL, led to a significant shift in the Nyquist plot. The results are promising regarding specific detection of clinically relevant concentrations of biomarkers, such as cardiac markers, with the newly developed microfluidic impedance biosensor chip.
format Online
Article
Text
id pubmed-8001378
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-80013782021-03-28 Microfluidic Impedance Biosensor Chips Using Sensing Layers Based on DNA-Based Self-Assembled Monolayers for Label-Free Detection of Proteins Alsabbagh, Khaled Hornung, Tim Voigt, Achim Sadir, Sahba Rajabi, Taleieh Länge, Kerstin Biosensors (Basel) Communication A microfluidic chip for electrochemical impedance spectroscopy (EIS) is presented as bio-sensor for label-free detection of proteins by using the example of cardiac troponin I. Troponin I is one of the most specific diagnostic serum biomarkers for myocardial infarction. The microfluidic impedance biosensor chip presented here consists of a microscope glass slide serving as base plate, sputtered electrodes, and a polydimethylsiloxane (PDMS) microchannel. Electrode functionalization protocols were developed considering a possible charge transfer through the sensing layer, in addition to analyte-specific binding by corresponding antibodies and reduction of nonspecific protein adsorption to prevent false-positive signals. Reagents tested for self-assembled monolayers (SAMs) on gold electrodes included thiolated hydrocarbons and thiolated oligonucleotides, where SAMs based on the latter showed a better performance. The corresponding antibody was covalently coupled on the SAM using carbodiimide chemistry. Sampling and measurement took only a few minutes. Application of a human serum albumin (HSA) sample, 1000 ng/mL, led to negligible impedance changes, while application of a troponin I sample, 1 ng/mL, led to a significant shift in the Nyquist plot. The results are promising regarding specific detection of clinically relevant concentrations of biomarkers, such as cardiac markers, with the newly developed microfluidic impedance biosensor chip. MDPI 2021-03-13 /pmc/articles/PMC8001378/ /pubmed/33805676 http://dx.doi.org/10.3390/bios11030080 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Communication
Alsabbagh, Khaled
Hornung, Tim
Voigt, Achim
Sadir, Sahba
Rajabi, Taleieh
Länge, Kerstin
Microfluidic Impedance Biosensor Chips Using Sensing Layers Based on DNA-Based Self-Assembled Monolayers for Label-Free Detection of Proteins
title Microfluidic Impedance Biosensor Chips Using Sensing Layers Based on DNA-Based Self-Assembled Monolayers for Label-Free Detection of Proteins
title_full Microfluidic Impedance Biosensor Chips Using Sensing Layers Based on DNA-Based Self-Assembled Monolayers for Label-Free Detection of Proteins
title_fullStr Microfluidic Impedance Biosensor Chips Using Sensing Layers Based on DNA-Based Self-Assembled Monolayers for Label-Free Detection of Proteins
title_full_unstemmed Microfluidic Impedance Biosensor Chips Using Sensing Layers Based on DNA-Based Self-Assembled Monolayers for Label-Free Detection of Proteins
title_short Microfluidic Impedance Biosensor Chips Using Sensing Layers Based on DNA-Based Self-Assembled Monolayers for Label-Free Detection of Proteins
title_sort microfluidic impedance biosensor chips using sensing layers based on dna-based self-assembled monolayers for label-free detection of proteins
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001378/
https://www.ncbi.nlm.nih.gov/pubmed/33805676
http://dx.doi.org/10.3390/bios11030080
work_keys_str_mv AT alsabbaghkhaled microfluidicimpedancebiosensorchipsusingsensinglayersbasedondnabasedselfassembledmonolayersforlabelfreedetectionofproteins
AT hornungtim microfluidicimpedancebiosensorchipsusingsensinglayersbasedondnabasedselfassembledmonolayersforlabelfreedetectionofproteins
AT voigtachim microfluidicimpedancebiosensorchipsusingsensinglayersbasedondnabasedselfassembledmonolayersforlabelfreedetectionofproteins
AT sadirsahba microfluidicimpedancebiosensorchipsusingsensinglayersbasedondnabasedselfassembledmonolayersforlabelfreedetectionofproteins
AT rajabitaleieh microfluidicimpedancebiosensorchipsusingsensinglayersbasedondnabasedselfassembledmonolayersforlabelfreedetectionofproteins
AT langekerstin microfluidicimpedancebiosensorchipsusingsensinglayersbasedondnabasedselfassembledmonolayersforlabelfreedetectionofproteins