Chemical gas-generating nanoparticles for tumor-targeted ultrasound imaging and ultrasound-triggered drug delivery

被引:58
|
作者
Min, Hyun Su [1 ]
Son, Sejin [1 ]
You, Dong Gil [1 ,2 ]
Lee, Tae Woong [1 ]
Lee, Jangwook [1 ]
Lee, Sangmin [1 ]
Yhee, Ji Young [1 ]
Lee, Jaeyoung [3 ]
Han, Moon Hee [3 ]
Park, Jae Hyung [2 ]
Kim, Sun Hwa [1 ]
Choi, Kuiwon [1 ]
Park, Kinam [5 ]
Kim, Kwangmeyung [1 ]
Kwon, Ick Chan [1 ,4 ]
机构
[1] Korea Inst Sci & Technol, Biomed Res Inst, Ctr Theragnosis, 39-1 Hawolgok Dong, Seoul 136791, South Korea
[2] Sungkyunkwan Univ, Sch Chem Engn, Suwon 440746, South Korea
[3] Seoul Natl Univ Hosp, Dept Radiol, 101 Daehangno, Seoul 110744, South Korea
[4] Korea Univ, KU KIST Sch, Seoul 136701, South Korea
[5] Purdue Univ, Dept Biomed Engn & Pharmaceut, W Lafayette, IN 47960 USA
关键词
Ultrasound (US) imaging; Ultrasound contrast agent (UCA); Chemical gas-generating nanoparticle; Tumor targeting; Drug delivery; MICROBUBBLES; NANOBUBBLES; RELEASE; PHASE;
D O I
10.1016/j.biomaterials.2016.08.049
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Although there is great versatility of ultrasound (US) technologies in the real clinical field, one main technical challenge is the compromising of high quality of echo properties and size engineering of ultrasound contrast agents (UCAs); a high echo property is offset by reducing particle size. Herein, a new strategy for overcoming the dilemma by devising chemical gas (CO2) generating carbonate copolymer nanoparticles (Gas-NPs), which are clearly distinguished from the conventional gas-encapsulated micro sized UCAs. More importantly, Gas-NPs could be readily engineered to strengthen the desirable in vivo physicochemical properties for nano-sized drug carriers with higher tumor targeting ability, as well as the high quality of echo properties for tumor-targeted US imaging. In tumor-bearing mice, anticancer drug-loaded Gas-NPs showed the desirable theranostic functions for US-triggered drug delivery, even after i.v. injection. In this regard, and as demonstrated in the aforementioned study, our technology could serve a highly effective platform in building theranostic UCAs with great sophistication and therapeutic applicability in tumor-targeted US imaging and US-triggered drug delivery. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:57 / 70
页数:14
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