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Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound
Recently, ultrasound (US)-based drug delivery strategies have received attention to improve enhanced permeation and retention (EPR) effect-based passive targeting efficiency of nanoparticles in vitro and in vivo conditions. Among the US treatment techniques, pulsed-high intensity focused ultrasound...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676802/ https://www.ncbi.nlm.nih.gov/pubmed/29170724 http://dx.doi.org/10.1186/s40580-017-0124-z |
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author | You, Dong Gil Yoon, Hong Yeol Jeon, Sangmin Um, Wooram Son, Sejin Park, Jae Hyung Kwon, Ick Chan Kim, Kwangmeyung |
author_facet | You, Dong Gil Yoon, Hong Yeol Jeon, Sangmin Um, Wooram Son, Sejin Park, Jae Hyung Kwon, Ick Chan Kim, Kwangmeyung |
author_sort | You, Dong Gil |
collection | PubMed |
description | Recently, ultrasound (US)-based drug delivery strategies have received attention to improve enhanced permeation and retention (EPR) effect-based passive targeting efficiency of nanoparticles in vitro and in vivo conditions. Among the US treatment techniques, pulsed-high intensity focused ultrasound (pHIFU) have specialized for improving tissue penetration of various macromolecules and nanoparticles without irreversible tissue damages. In this study, we have demonstrated that pHIFU could be utilized to improve tissue penetration of fluorescent dye-labeled glycol chitosan nanoparticles (FCNPs) in femoral tissue of mice. pHIFU could improve blood flow of the targeted-blood vessel in femoral tissue. In addition, tissue penetration of FCNPs was specifically increased 5.7-, 8- and 9.3-folds than that of non-treated (0 W pHIFU) femoral tissue, when the femoral tissue was treated with 10, 20 and 50 W of pHIFU, respectively. However, tissue penetration of FCNPs was significantly reduced after 3 h post-pHIFU treatment (50 W). Because overdose (50 W) of pHIFU led to irreversible tissue damages, including the edema and chapped red blood cells. These overall results support that pHIFU treatment can enhance the extravasation and tissue penetration of FCNPs as well as induce irreversible tissue damages. We expect that our results can provide advantages to optimize pHIFU-mediated delivery strategy of nanoparticles for further clinical applications. |
format | Online Article Text |
id | pubmed-5676802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-56768022017-11-21 Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound You, Dong Gil Yoon, Hong Yeol Jeon, Sangmin Um, Wooram Son, Sejin Park, Jae Hyung Kwon, Ick Chan Kim, Kwangmeyung Nano Converg Research Recently, ultrasound (US)-based drug delivery strategies have received attention to improve enhanced permeation and retention (EPR) effect-based passive targeting efficiency of nanoparticles in vitro and in vivo conditions. Among the US treatment techniques, pulsed-high intensity focused ultrasound (pHIFU) have specialized for improving tissue penetration of various macromolecules and nanoparticles without irreversible tissue damages. In this study, we have demonstrated that pHIFU could be utilized to improve tissue penetration of fluorescent dye-labeled glycol chitosan nanoparticles (FCNPs) in femoral tissue of mice. pHIFU could improve blood flow of the targeted-blood vessel in femoral tissue. In addition, tissue penetration of FCNPs was specifically increased 5.7-, 8- and 9.3-folds than that of non-treated (0 W pHIFU) femoral tissue, when the femoral tissue was treated with 10, 20 and 50 W of pHIFU, respectively. However, tissue penetration of FCNPs was significantly reduced after 3 h post-pHIFU treatment (50 W). Because overdose (50 W) of pHIFU led to irreversible tissue damages, including the edema and chapped red blood cells. These overall results support that pHIFU treatment can enhance the extravasation and tissue penetration of FCNPs as well as induce irreversible tissue damages. We expect that our results can provide advantages to optimize pHIFU-mediated delivery strategy of nanoparticles for further clinical applications. Springer Singapore 2017-11-08 /pmc/articles/PMC5676802/ /pubmed/29170724 http://dx.doi.org/10.1186/s40580-017-0124-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research You, Dong Gil Yoon, Hong Yeol Jeon, Sangmin Um, Wooram Son, Sejin Park, Jae Hyung Kwon, Ick Chan Kim, Kwangmeyung Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound |
title | Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound |
title_full | Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound |
title_fullStr | Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound |
title_full_unstemmed | Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound |
title_short | Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound |
title_sort | deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676802/ https://www.ncbi.nlm.nih.gov/pubmed/29170724 http://dx.doi.org/10.1186/s40580-017-0124-z |
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