Multifrequency bioimpedance device based on the Analog Discovery 2: performance and characterization

Bioimpedance spectroscopy can be used to investigate the composition and monitor the human body, organs, tissues, or cell cultures by measuring the voltage developed by the injection of small alternating currents at different frequencies. These currents are injected sequentially through a frequency...

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Published in:Current Directions in Biomedical Engineering
Main Authors: Battistel Alberto, Craamer Lizarraga Hegoa, Termenon Maite, Möller Knut
Format: Article
Language:English
Published: De Gruyter 2023-09-01
Subjects:
Online Access:https://doi.org/10.1515/cdbme-2023-1134
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author Battistel Alberto
Craamer Lizarraga Hegoa
Termenon Maite
Möller Knut
author_facet Battistel Alberto
Craamer Lizarraga Hegoa
Termenon Maite
Möller Knut
author_sort Battistel Alberto
collection DOAJ
container_title Current Directions in Biomedical Engineering
description Bioimpedance spectroscopy can be used to investigate the composition and monitor the human body, organs, tissues, or cell cultures by measuring the voltage developed by the injection of small alternating currents at different frequencies. These currents are injected sequentially through a frequency sweep and a with a Howland current source or one of its modifications. However, the frequency sweep is not time efficient and introduces problems with data coherence in the case of bioinstability. On the other hand, the Howland current source requires high precision matching between its components. In this contribution we developed a custom-made device for bioimpedance measurements based on a multisine current waveform and on a negative-feedback topology for the current source. Measurements on passive elements showed that the device had less than 1Ω and 0.05∘ uncertainty in the frequency range between 500 Hz and 200 kHz for impedance between 1 kΩ and 10 kΩ. The measurements were affected by an inductive artifact connected with the limited common-mode rejection at high frequencies. Nevertheless, we could characterize the artifacts through a fitting procedure to recover the expected value of the targeted impedance.
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spelling doaj-art-9727c7660dfc40b6904e38b3b8dd17bb2025-08-20T00:10:28ZengDe GruyterCurrent Directions in Biomedical Engineering2364-55042023-09-019153653910.1515/cdbme-2023-1134Multifrequency bioimpedance device based on the Analog Discovery 2: performance and characterizationBattistel Alberto0Craamer Lizarraga Hegoa1Termenon Maite2Möller Knut3Institute of Technical Medicine (ITeM), Furtwangen University, Jakob-Kienzle-Strasse 17, 78054Villingen-Schwenningen, GermanyBiomedical Engineering Department, Faculty of Engineering, Mondragon Unibertsitatea (MU-ENG), Loramendi, 4; 20500Mondragón, SpainBiomedical Engineering Department, Faculty of Engineering, Mondragon Unibertsitatea (MU-ENG), Loramendi, 4; 20500Mondragón, SpainInstitute of Technical Medicine (ITeM), Furtwangen University, 78054Villingen-Schwenningen, GermanyBioimpedance spectroscopy can be used to investigate the composition and monitor the human body, organs, tissues, or cell cultures by measuring the voltage developed by the injection of small alternating currents at different frequencies. These currents are injected sequentially through a frequency sweep and a with a Howland current source or one of its modifications. However, the frequency sweep is not time efficient and introduces problems with data coherence in the case of bioinstability. On the other hand, the Howland current source requires high precision matching between its components. In this contribution we developed a custom-made device for bioimpedance measurements based on a multisine current waveform and on a negative-feedback topology for the current source. Measurements on passive elements showed that the device had less than 1Ω and 0.05∘ uncertainty in the frequency range between 500 Hz and 200 kHz for impedance between 1 kΩ and 10 kΩ. The measurements were affected by an inductive artifact connected with the limited common-mode rejection at high frequencies. Nevertheless, we could characterize the artifacts through a fitting procedure to recover the expected value of the targeted impedance.https://doi.org/10.1515/cdbme-2023-1134bioimpedanceimpedance spectroscopyfpgaanalog discovery 2multisinebroadband excitationinstrumentation amplifiercommon-mode rejectionmultifrequencycurrent source
spellingShingle Battistel Alberto
Craamer Lizarraga Hegoa
Termenon Maite
Möller Knut
Multifrequency bioimpedance device based on the Analog Discovery 2: performance and characterization
bioimpedance
impedance spectroscopy
fpga
analog discovery 2
multisine
broadband excitation
instrumentation amplifier
common-mode rejection
multifrequency
current source
title Multifrequency bioimpedance device based on the Analog Discovery 2: performance and characterization
title_full Multifrequency bioimpedance device based on the Analog Discovery 2: performance and characterization
title_fullStr Multifrequency bioimpedance device based on the Analog Discovery 2: performance and characterization
title_full_unstemmed Multifrequency bioimpedance device based on the Analog Discovery 2: performance and characterization
title_short Multifrequency bioimpedance device based on the Analog Discovery 2: performance and characterization
title_sort multifrequency bioimpedance device based on the analog discovery 2 performance and characterization
topic bioimpedance
impedance spectroscopy
fpga
analog discovery 2
multisine
broadband excitation
instrumentation amplifier
common-mode rejection
multifrequency
current source
url https://doi.org/10.1515/cdbme-2023-1134
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AT termenonmaite multifrequencybioimpedancedevicebasedontheanalogdiscovery2performanceandcharacterization
AT mollerknut multifrequencybioimpedancedevicebasedontheanalogdiscovery2performanceandcharacterization