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Experimental research on surface acoustic wave microfluidic atomization for drug delivery
This paper demonstrates that surface acoustic wave (SAW) atomization can produce suitable aerosol concentration and size distribution for efficient inhaled lung drug delivery and is a potential atomization device for asthma treatment. Using the SAW device, we present comprehensive experimental resul...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106708/ https://www.ncbi.nlm.nih.gov/pubmed/35562384 http://dx.doi.org/10.1038/s41598-022-11132-9 |
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author | Huang, Qing-Yun Le, Ying Hu, Hong Wan, Zhi-jian Ning, Jia Han, Jun-Long |
author_facet | Huang, Qing-Yun Le, Ying Hu, Hong Wan, Zhi-jian Ning, Jia Han, Jun-Long |
author_sort | Huang, Qing-Yun |
collection | PubMed |
description | This paper demonstrates that surface acoustic wave (SAW) atomization can produce suitable aerosol concentration and size distribution for efficient inhaled lung drug delivery and is a potential atomization device for asthma treatment. Using the SAW device, we present comprehensive experimental results exploring the complexity of the acoustic atomization process and the influence of input power, device frequency, and liquid flow rate on aerosol size distribution. It is hoped that these studies will explain the mechanism of SAW atomization aerosol generation and how they can be controlled. The insights from the high-speed flow visualization studies reveal that it is possible by setting the input power above 4.17 W, thus allowing atomization to occur from a relatively thin film, forming dense, monodisperse aerosols. Moreover, we found that the aerosol droplet size can be effectively changed by adjusting the input power and liquid flow rate to change the film conditions. In this work, we proposed a method to realize drug atomization by a microfluidic channel. A SU-8 flow channel was prepared on the surface of a piezoelectric substrate by photolithography technology. Combined with the silicon dioxide coating process and PDMS process closed microfluidic channel was prepared, and continuous drug atomization was provided to improve the deposition efficiency of drug atomization by microfluidic. |
format | Online Article Text |
id | pubmed-9106708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91067082022-05-15 Experimental research on surface acoustic wave microfluidic atomization for drug delivery Huang, Qing-Yun Le, Ying Hu, Hong Wan, Zhi-jian Ning, Jia Han, Jun-Long Sci Rep Article This paper demonstrates that surface acoustic wave (SAW) atomization can produce suitable aerosol concentration and size distribution for efficient inhaled lung drug delivery and is a potential atomization device for asthma treatment. Using the SAW device, we present comprehensive experimental results exploring the complexity of the acoustic atomization process and the influence of input power, device frequency, and liquid flow rate on aerosol size distribution. It is hoped that these studies will explain the mechanism of SAW atomization aerosol generation and how they can be controlled. The insights from the high-speed flow visualization studies reveal that it is possible by setting the input power above 4.17 W, thus allowing atomization to occur from a relatively thin film, forming dense, monodisperse aerosols. Moreover, we found that the aerosol droplet size can be effectively changed by adjusting the input power and liquid flow rate to change the film conditions. In this work, we proposed a method to realize drug atomization by a microfluidic channel. A SU-8 flow channel was prepared on the surface of a piezoelectric substrate by photolithography technology. Combined with the silicon dioxide coating process and PDMS process closed microfluidic channel was prepared, and continuous drug atomization was provided to improve the deposition efficiency of drug atomization by microfluidic. Nature Publishing Group UK 2022-05-13 /pmc/articles/PMC9106708/ /pubmed/35562384 http://dx.doi.org/10.1038/s41598-022-11132-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Huang, Qing-Yun Le, Ying Hu, Hong Wan, Zhi-jian Ning, Jia Han, Jun-Long Experimental research on surface acoustic wave microfluidic atomization for drug delivery |
title | Experimental research on surface acoustic wave microfluidic atomization for drug delivery |
title_full | Experimental research on surface acoustic wave microfluidic atomization for drug delivery |
title_fullStr | Experimental research on surface acoustic wave microfluidic atomization for drug delivery |
title_full_unstemmed | Experimental research on surface acoustic wave microfluidic atomization for drug delivery |
title_short | Experimental research on surface acoustic wave microfluidic atomization for drug delivery |
title_sort | experimental research on surface acoustic wave microfluidic atomization for drug delivery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106708/ https://www.ncbi.nlm.nih.gov/pubmed/35562384 http://dx.doi.org/10.1038/s41598-022-11132-9 |
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