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On‐chip label‐free impedance‐based detection of antibiotic permeation

Biosensors are analytical tools used for the analysis of biomaterial samples and provide an understanding about the biocomposition, structure, and function of biomolecules and/or biomechanisms by converting the biological response into an electrical and/or optical signal. In particular, with the ris...

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Autores principales: Kaur, Jaspreet, Ghorbanpoor, Hamed, Öztürk, Yasin, Kaygusuz, Özge, Avcı, Hüseyin, Darcan, Cihan, Trabzon, Levent, Güzel, Fatma D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675796/
https://www.ncbi.nlm.nih.gov/pubmed/34694729
http://dx.doi.org/10.1049/nbt2.12019
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author Kaur, Jaspreet
Ghorbanpoor, Hamed
Öztürk, Yasin
Kaygusuz, Özge
Avcı, Hüseyin
Darcan, Cihan
Trabzon, Levent
Güzel, Fatma D.
author_facet Kaur, Jaspreet
Ghorbanpoor, Hamed
Öztürk, Yasin
Kaygusuz, Özge
Avcı, Hüseyin
Darcan, Cihan
Trabzon, Levent
Güzel, Fatma D.
author_sort Kaur, Jaspreet
collection PubMed
description Biosensors are analytical tools used for the analysis of biomaterial samples and provide an understanding about the biocomposition, structure, and function of biomolecules and/or biomechanisms by converting the biological response into an electrical and/or optical signal. In particular, with the rise in antibiotic resistance amongst pathogenic bacteria, the study of antibiotic activity and transport across cell membranes in the field of biosensors has been gaining widespread importance. Herein, for the rapid and label‐free detection of antibiotic permeation across a membrane, a microelectrode integrated microfluidic device is presented. The integrated chip consists of polydimethylsiloxane based microfluidic channels bonded onto microelectrodes on‐glass and enables us to recognize the antibiotic permeation across a membrane into the model membranes based on electrical impedance measurement, while also allowing optical monitoring. Impedance testing is label free and therefore allows the detection of both fluorescent and non‐fluorescent antibiotics. As a model membrane, Giant Unilamellar Vesicles (GUVs) are used and impedance measurements were performed by a precision inductance, capacitance, and resistance metre. The measured signal recorded from the device was used to determine the change in concentration inside and outside of the GUVs. We have found that permeation of antibiotic molecules can be easily monitored over time using the proposed integrated device. The results also show a clear difference between bilayer permeation that occurs through the lipidic bilayer and porin‐mediated permeation through the porin channels inserted in the lipid bilayer.
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spelling pubmed-86757962022-02-03 On‐chip label‐free impedance‐based detection of antibiotic permeation Kaur, Jaspreet Ghorbanpoor, Hamed Öztürk, Yasin Kaygusuz, Özge Avcı, Hüseyin Darcan, Cihan Trabzon, Levent Güzel, Fatma D. IET Nanobiotechnol Original Research Papers Biosensors are analytical tools used for the analysis of biomaterial samples and provide an understanding about the biocomposition, structure, and function of biomolecules and/or biomechanisms by converting the biological response into an electrical and/or optical signal. In particular, with the rise in antibiotic resistance amongst pathogenic bacteria, the study of antibiotic activity and transport across cell membranes in the field of biosensors has been gaining widespread importance. Herein, for the rapid and label‐free detection of antibiotic permeation across a membrane, a microelectrode integrated microfluidic device is presented. The integrated chip consists of polydimethylsiloxane based microfluidic channels bonded onto microelectrodes on‐glass and enables us to recognize the antibiotic permeation across a membrane into the model membranes based on electrical impedance measurement, while also allowing optical monitoring. Impedance testing is label free and therefore allows the detection of both fluorescent and non‐fluorescent antibiotics. As a model membrane, Giant Unilamellar Vesicles (GUVs) are used and impedance measurements were performed by a precision inductance, capacitance, and resistance metre. The measured signal recorded from the device was used to determine the change in concentration inside and outside of the GUVs. We have found that permeation of antibiotic molecules can be easily monitored over time using the proposed integrated device. The results also show a clear difference between bilayer permeation that occurs through the lipidic bilayer and porin‐mediated permeation through the porin channels inserted in the lipid bilayer. John Wiley and Sons Inc. 2021-02-02 /pmc/articles/PMC8675796/ /pubmed/34694729 http://dx.doi.org/10.1049/nbt2.12019 Text en © 2021 The Authors. IET Nanobiotechnology published by John Wiley & Sons Ltd on behalf of The Institution of Engineering and Technology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Papers
Kaur, Jaspreet
Ghorbanpoor, Hamed
Öztürk, Yasin
Kaygusuz, Özge
Avcı, Hüseyin
Darcan, Cihan
Trabzon, Levent
Güzel, Fatma D.
On‐chip label‐free impedance‐based detection of antibiotic permeation
title On‐chip label‐free impedance‐based detection of antibiotic permeation
title_full On‐chip label‐free impedance‐based detection of antibiotic permeation
title_fullStr On‐chip label‐free impedance‐based detection of antibiotic permeation
title_full_unstemmed On‐chip label‐free impedance‐based detection of antibiotic permeation
title_short On‐chip label‐free impedance‐based detection of antibiotic permeation
title_sort on‐chip label‐free impedance‐based detection of antibiotic permeation
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675796/
https://www.ncbi.nlm.nih.gov/pubmed/34694729
http://dx.doi.org/10.1049/nbt2.12019
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