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

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2021Author
Kaur, JaspreetGhorbanpoor, Hamed
Öztürk, Yasin
Kaygusuz, Özge
Avcı, Hüseyin
Darcan, Cihan
Trabzon, Levent
Doğan Güzel, Fatma
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Kaur, J., Ghorbanpoor, H., Öztürk, Y., Kaygusuz, Ö., Avcı, H., Darcan, C., ... & Güzel, F. D. (2021). On‐chip label‐free impedance‐based detection of antibiotic permeation. IET nanobiotechnology, 15(1), 100-106.Abstract
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 mea-
surements 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.