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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...

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Autores principales: You, Dong Gil, Yoon, Hong Yeol, Jeon, Sangmin, Um, Wooram, Son, Sejin, Park, Jae Hyung, Kwon, Ick Chan, Kim, Kwangmeyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2017
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.
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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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