MULTIPLE-EXPOSURE DRUG RELEASE FROM STABLE NANODROPLETS BY HIGH-INTENSITY FOCUSED ULTRASOUND FOR A POTENTIAL DEGENERATIVE DISC DISEASE TREATMENT

被引:10
作者
Khoi Nguyen [1 ]
Pan, Hsuan-Yeh [2 ,5 ]
Haworth, Kevin [1 ,2 ]
Mahoney, Eric [1 ,6 ]
Mercado-Shekhar, Karla P. [2 ]
Lin, Chia-Ying [3 ]
Zhang, Zhe [4 ]
Park, Yoonjee C. [1 ,4 ]
机构
[1] Univ Cincinnati, Dept Biomed Engn, Cincinnati, OH USA
[2] Univ Cincinnati, Dept Internal Med, Cincinnati, OH USA
[3] Univ Cincinnati, Dept Orthopaed Surg, Cincinnati, OH USA
[4] Univ Cincinnati, Dept Environm Chem & Engn, 2901 Woodside Dr, Cincinnati, OH 45221 USA
[5] Indiana Univ, Sch Optometry, Bloomington, IN 47405 USA
[6] POB 100942, Arlington, VA 22210 USA
基金
美国国家卫生研究院;
关键词
High-intensity focused ultrasound; On-demand drug release; Multiple releases; Degenerative disc disease; PHASE-SHIFT; MICROBUBBLES; SIMVASTATIN; DELIVERY;
D O I
10.1016/j.ultrasmedbio.2018.09.014
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
The combination of simvastatin and CF680 dye encapsulated by stable nanodroplets has been developed as a drug delivery carrier. Simvastatin has previously been found to be a potential degenerative disc disease treatment. Multiple exposures of the nanodroplets to high-intensity focused ultrasound induced release of simvastatin. Each ultrasound exposure yielded a consistent concentration of the drug and dye released. B-mode ultrasound image analysis data and cavitation data clearly indicated the release mechanism is phase transition of the liquid nanodroplets into gas bubbles. The nanodroplets were stably stored in ex vivo rabbit spinal discs for at least 14 days, and the contents responded to ultrasound exposure on demand. Lastly, nucleus pulposus cells harvested from rabbit spine discs and exposed to media with nanodroplets exhibited a decrease in cell viability (85%) relative to the cells only (96.7%) at 24 h, but no difference at 48 h. Thus, the system may be a potential degenerative disc disease treatment. (C) 2018 World Federation for Ultrasound in Medicine & Biology. All rights reserved.
引用
收藏
页码:160 / 169
页数:10
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