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Capillary flow in microchannel circuitry of scleral lenses

Continuous monitoring of biomarkers in a quantitative manner at point-of-care settings can advance early diagnosis in medicine. Contact lenses offer a minimally-invasive platform to continuously detect biomarkers in tear fluid. Microfluidic components as lab-on-a-chip technology have the potential t...

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Autores principales: Yetisen, Ali K., Soylemezoglu, Bugra, Dong, Jie, Montelongo, Yunuen, Butt, Haider, Jakobi, Martin, Koch, Alexander W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063415/
https://www.ncbi.nlm.nih.gov/pubmed/35520217
http://dx.doi.org/10.1039/c9ra01094g
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author Yetisen, Ali K.
Soylemezoglu, Bugra
Dong, Jie
Montelongo, Yunuen
Butt, Haider
Jakobi, Martin
Koch, Alexander W.
author_facet Yetisen, Ali K.
Soylemezoglu, Bugra
Dong, Jie
Montelongo, Yunuen
Butt, Haider
Jakobi, Martin
Koch, Alexander W.
author_sort Yetisen, Ali K.
collection PubMed
description Continuous monitoring of biomarkers in a quantitative manner at point-of-care settings can advance early diagnosis in medicine. Contact lenses offer a minimally-invasive platform to continuously detect biomarkers in tear fluid. Microfluidic components as lab-on-a-chip technology have the potential to transform contact lenses into fully-integrated multiplexed sensing devices. Here, simple and complex microchannels are created in scleral lenses that perform microfluidic operations via capillary action. The engraving of microchannels in scleral lenses were performed by laser micromilling, where a predictive computational model was developed to simulate the effect of laser power and exposure time on polymer behavior. Experimentally varying the CO(2) laser power (1.2–3.6 W) and speed (38–100 mm s(−1)) allowed the micromilling of concave microchannels with groove depths of 10–240 μm and widths of 35–245 μm on polymetric substrates. The demonstrated laser micromilled circuitry in scleral lenses included linear channels, T/Y junctions, multiplexed arrays, mixers, and spiral channels, as well as serially organized multicomponent channels. Capillary forces acting in the microchannels allowed flowing rhodamine dye within the microfluidic components, which was visualized by optical microscopy in reflection and transmission modes simultaneously. The developed microfluidic components in scleral lenses may enable tear sampling, storage, analysis, and multiplexed detection capabilities for continuous monitoring applications.
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spelling pubmed-90634152022-05-04 Capillary flow in microchannel circuitry of scleral lenses Yetisen, Ali K. Soylemezoglu, Bugra Dong, Jie Montelongo, Yunuen Butt, Haider Jakobi, Martin Koch, Alexander W. RSC Adv Chemistry Continuous monitoring of biomarkers in a quantitative manner at point-of-care settings can advance early diagnosis in medicine. Contact lenses offer a minimally-invasive platform to continuously detect biomarkers in tear fluid. Microfluidic components as lab-on-a-chip technology have the potential to transform contact lenses into fully-integrated multiplexed sensing devices. Here, simple and complex microchannels are created in scleral lenses that perform microfluidic operations via capillary action. The engraving of microchannels in scleral lenses were performed by laser micromilling, where a predictive computational model was developed to simulate the effect of laser power and exposure time on polymer behavior. Experimentally varying the CO(2) laser power (1.2–3.6 W) and speed (38–100 mm s(−1)) allowed the micromilling of concave microchannels with groove depths of 10–240 μm and widths of 35–245 μm on polymetric substrates. The demonstrated laser micromilled circuitry in scleral lenses included linear channels, T/Y junctions, multiplexed arrays, mixers, and spiral channels, as well as serially organized multicomponent channels. Capillary forces acting in the microchannels allowed flowing rhodamine dye within the microfluidic components, which was visualized by optical microscopy in reflection and transmission modes simultaneously. The developed microfluidic components in scleral lenses may enable tear sampling, storage, analysis, and multiplexed detection capabilities for continuous monitoring applications. The Royal Society of Chemistry 2019-04-09 /pmc/articles/PMC9063415/ /pubmed/35520217 http://dx.doi.org/10.1039/c9ra01094g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yetisen, Ali K.
Soylemezoglu, Bugra
Dong, Jie
Montelongo, Yunuen
Butt, Haider
Jakobi, Martin
Koch, Alexander W.
Capillary flow in microchannel circuitry of scleral lenses
title Capillary flow in microchannel circuitry of scleral lenses
title_full Capillary flow in microchannel circuitry of scleral lenses
title_fullStr Capillary flow in microchannel circuitry of scleral lenses
title_full_unstemmed Capillary flow in microchannel circuitry of scleral lenses
title_short Capillary flow in microchannel circuitry of scleral lenses
title_sort capillary flow in microchannel circuitry of scleral lenses
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063415/
https://www.ncbi.nlm.nih.gov/pubmed/35520217
http://dx.doi.org/10.1039/c9ra01094g
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