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Compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring

Premature neonates are too small for repeated blood sampling, but still require precise monitoring of blood gas levels. The standard method therefore involves transcutaneous blood gas monitoring (TBM), i.e. analyzing gas that permeates the skin. The method involves skin heating and requires frequent...

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Detalles Bibliográficos
Autores principales: Seton, Ragnar, Thornell, Greger, Persson, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056951/
https://www.ncbi.nlm.nih.gov/pubmed/35517952
http://dx.doi.org/10.1039/d0ra03877f
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author Seton, Ragnar
Thornell, Greger
Persson, Anders
author_facet Seton, Ragnar
Thornell, Greger
Persson, Anders
author_sort Seton, Ragnar
collection PubMed
description Premature neonates are too small for repeated blood sampling, but still require precise monitoring of blood gas levels. The standard method therefore involves transcutaneous blood gas monitoring (TBM), i.e. analyzing gas that permeates the skin. The method involves skin heating and requires frequent relocation of a rigid sensor that is adhesively mounted to the skin, which makes the monitoring intermittent and can cause tissue damage. To mitigate this, this paper introduces a TBM concept that replaces the sensor with a small, non-adhesive, flexible, polydimethylsiloxane patch, routing the gases through skin-facing microchannels laid out in various configurations, to an external optical emission spectroscopy system (OES). As the OES depends on a constant flow of gas, we have investigated the effects external loads, both vertical and with a transverse component, have on the aerodynamic resistance of the patches. The experiments show that patches with 200 μm wide channels can withstand uniformly distributed forces up to 25 N with a change in aerodynamic resistance of about 0.01 mbar per sccm per newton. In subsequent measurements, the proof of concept (POC) TBM system showed a strong and fast blood gas signal that was unaffected by all likely loads in the intended application. Moreover, the rise time of the signal is shown to be inversely proportional to the aerodynamic resistance, and the signal strength to be proportional to the skin area exposed to the microchannels. With these results, the POC TBM system is a viable first step towards truly continuous blood gas monitoring of prematurely born children.
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spelling pubmed-90569512022-05-04 Compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring Seton, Ragnar Thornell, Greger Persson, Anders RSC Adv Chemistry Premature neonates are too small for repeated blood sampling, but still require precise monitoring of blood gas levels. The standard method therefore involves transcutaneous blood gas monitoring (TBM), i.e. analyzing gas that permeates the skin. The method involves skin heating and requires frequent relocation of a rigid sensor that is adhesively mounted to the skin, which makes the monitoring intermittent and can cause tissue damage. To mitigate this, this paper introduces a TBM concept that replaces the sensor with a small, non-adhesive, flexible, polydimethylsiloxane patch, routing the gases through skin-facing microchannels laid out in various configurations, to an external optical emission spectroscopy system (OES). As the OES depends on a constant flow of gas, we have investigated the effects external loads, both vertical and with a transverse component, have on the aerodynamic resistance of the patches. The experiments show that patches with 200 μm wide channels can withstand uniformly distributed forces up to 25 N with a change in aerodynamic resistance of about 0.01 mbar per sccm per newton. In subsequent measurements, the proof of concept (POC) TBM system showed a strong and fast blood gas signal that was unaffected by all likely loads in the intended application. Moreover, the rise time of the signal is shown to be inversely proportional to the aerodynamic resistance, and the signal strength to be proportional to the skin area exposed to the microchannels. With these results, the POC TBM system is a viable first step towards truly continuous blood gas monitoring of prematurely born children. The Royal Society of Chemistry 2020-10-05 /pmc/articles/PMC9056951/ /pubmed/35517952 http://dx.doi.org/10.1039/d0ra03877f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Seton, Ragnar
Thornell, Greger
Persson, Anders
Compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring
title Compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring
title_full Compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring
title_fullStr Compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring
title_full_unstemmed Compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring
title_short Compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring
title_sort compliance of a microstructured, soft sampling device for transcutaneous blood gas monitoring
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056951/
https://www.ncbi.nlm.nih.gov/pubmed/35517952
http://dx.doi.org/10.1039/d0ra03877f
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