Microfluidics Integration into Low-Noise Multi-Electrode Arrays

Organ-on-Chip technology is commonly used as a tool to replace animal testing in drug development. Cells or tissues are cultured on a microchip to replicate organ-level functions, where measurements of the electrical activity can be taken to understand how the cell populations react to different dru...

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Main Authors: Mafalda Ribeiro, Pamela Ali, Benjamin Metcalfe, Despina Moschou, Paulo R. F. Rocha
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Micromachines
Subjects:
MEA
Online Access:https://www.mdpi.com/2072-666X/12/6/727
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spelling doaj-51db6724e2d84662ad99823147d9d6ae2021-07-01T00:41:53ZengMDPI AGMicromachines2072-666X2021-06-011272772710.3390/mi12060727Microfluidics Integration into Low-Noise Multi-Electrode ArraysMafalda Ribeiro0Pamela Ali1Benjamin Metcalfe2Despina Moschou3Paulo R. F. Rocha4Centre for Accountable, Responsible, and Transparent AI (ART-AI), Department of Computer Science, University of Bath, Bath BA2 7AY, UKCentre for Biosensors, Bioelectronics, and Biodevices (C3Bio), Department of Electronic and Electrical Engineering, University of Bath, Bath BA2 7AY, UKCentre for Biosensors, Bioelectronics, and Biodevices (C3Bio), Department of Electronic and Electrical Engineering, University of Bath, Bath BA2 7AY, UKCentre for Biosensors, Bioelectronics, and Biodevices (C3Bio), Department of Electronic and Electrical Engineering, University of Bath, Bath BA2 7AY, UKCentre for Functional Ecology (CFE), Department of Life Sciences, University of Coimbra, 3000-456 Coimbra, PortugalOrgan-on-Chip technology is commonly used as a tool to replace animal testing in drug development. Cells or tissues are cultured on a microchip to replicate organ-level functions, where measurements of the electrical activity can be taken to understand how the cell populations react to different drugs. Microfluidic structures are integrated in these devices to replicate more closely an in vivo microenvironment. Research has provided proof of principle that more accurate replications of the microenvironment result in better micro-physiological behaviour, which in turn results in a higher predictive power. This work shows a transition from a no-flow (static) multi-electrode array (MEA) to a continuous-flow (dynamic) MEA, assuring a continuous and homogeneous transfer of an electrolyte solution across the measurement chamber. The process through which the microfluidic system was designed, simulated, and fabricated is described, and electrical characterisation of the whole structure under static solution and a continuous flow rate of 80 µL/min was performed. The latter reveals minimal background disturbance, with a background noise below 30 µVpp for all flow rates and areas. This microfluidic MEA, therefore, opens new avenues for more accurate and long-term recordings in Organ-on-Chip systems.https://www.mdpi.com/2072-666X/12/6/727MEAbrain cellselectrical recordingsOrgan-on-ChipmicrofluidicsBrain-on-Chip
collection DOAJ
language English
format Article
sources DOAJ
author Mafalda Ribeiro
Pamela Ali
Benjamin Metcalfe
Despina Moschou
Paulo R. F. Rocha
spellingShingle Mafalda Ribeiro
Pamela Ali
Benjamin Metcalfe
Despina Moschou
Paulo R. F. Rocha
Microfluidics Integration into Low-Noise Multi-Electrode Arrays
Micromachines
MEA
brain cells
electrical recordings
Organ-on-Chip
microfluidics
Brain-on-Chip
author_facet Mafalda Ribeiro
Pamela Ali
Benjamin Metcalfe
Despina Moschou
Paulo R. F. Rocha
author_sort Mafalda Ribeiro
title Microfluidics Integration into Low-Noise Multi-Electrode Arrays
title_short Microfluidics Integration into Low-Noise Multi-Electrode Arrays
title_full Microfluidics Integration into Low-Noise Multi-Electrode Arrays
title_fullStr Microfluidics Integration into Low-Noise Multi-Electrode Arrays
title_full_unstemmed Microfluidics Integration into Low-Noise Multi-Electrode Arrays
title_sort microfluidics integration into low-noise multi-electrode arrays
publisher MDPI AG
series Micromachines
issn 2072-666X
publishDate 2021-06-01
description Organ-on-Chip technology is commonly used as a tool to replace animal testing in drug development. Cells or tissues are cultured on a microchip to replicate organ-level functions, where measurements of the electrical activity can be taken to understand how the cell populations react to different drugs. Microfluidic structures are integrated in these devices to replicate more closely an in vivo microenvironment. Research has provided proof of principle that more accurate replications of the microenvironment result in better micro-physiological behaviour, which in turn results in a higher predictive power. This work shows a transition from a no-flow (static) multi-electrode array (MEA) to a continuous-flow (dynamic) MEA, assuring a continuous and homogeneous transfer of an electrolyte solution across the measurement chamber. The process through which the microfluidic system was designed, simulated, and fabricated is described, and electrical characterisation of the whole structure under static solution and a continuous flow rate of 80 µL/min was performed. The latter reveals minimal background disturbance, with a background noise below 30 µVpp for all flow rates and areas. This microfluidic MEA, therefore, opens new avenues for more accurate and long-term recordings in Organ-on-Chip systems.
topic MEA
brain cells
electrical recordings
Organ-on-Chip
microfluidics
Brain-on-Chip
url https://www.mdpi.com/2072-666X/12/6/727
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AT despinamoschou microfluidicsintegrationintolownoisemultielectrodearrays
AT paulorfrocha microfluidicsintegrationintolownoisemultielectrodearrays
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