Deep tissue penetration of nanoparticles using pulsed-high intensity focused ultrasound

被引:14
|
作者
You, Dong Gil [1 ,2 ]
Yoon, Hong Yeol [2 ]
Jeon, Sangmin [1 ,2 ]
Um, Wooram [1 ,2 ]
Son, Sejin [2 ]
Park, Jae Hyung [1 ]
Kwon, Ick Chan [2 ,3 ]
Kim, Kwangmeyung [2 ,3 ]
机构
[1] Sungkyunkwan Univ, Sch Chem Engn, 2066 Seobu Ro, Suwon 16419, South Korea
[2] Korea Inst Sci & Technol, Biomed Res Inst, Ctr Theragnosi s, 5,Hwarang Ro 14 Gil, Seoul 02792, South Korea
[3] Korea Univ, KU KIST Grad Sch Converging Sci & Technol, 145 Anam Ro, Seoul 02841, South Korea
来源
NANO CONVERGENCE | 2017年 / 4卷
关键词
Pulsed-high intensity focused ultrasound; Tissue penetration; Nanoparticle; Drug delivery;
D O I
10.1186/s40580-017-0124-z
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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 (0W pHIFU) femoral tissue, when the femoral tissue was treated with 10, 20 and 50W of pHIFU, respectively. However, tissue penetration of FCNPs was significantly reduced after 3 h post-pHIFU treatment (50W). Because overdose (50W) 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.
引用
收藏
页数:10
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