Experimental research on surface acoustic wave microfluidic atomization for drug delivery

被引:16
作者
Huang, Qing-Yun [1 ,2 ]
Le, Ying [3 ]
Hu, Hong [1 ]
Wan, Zhi-jian [2 ]
Ning, Jia [1 ]
Han, Jun-Long [1 ]
机构
[1] Harbin Inst Technol Shenzhen, Sch Mech Engn & Automat, Shenzhen 518055, Guangdong, Peoples R China
[2] Shenzhen Polytech, Shenzhen 518055, Peoples R China
[3] Southern Univ Sci & Technol, Jinan Univ, Affiliated Hosp 1, Shenzhen Peoples Hosp,Clin Med Coll 2,Dept Endocr, Shenzhen 518020, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
NEBULIZER; EFFICACY; THERAPY;
D O I
10.1038/s41598-022-11132-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This paper demonstrates that surface acoustic wave (SAW) atomization can produce suitable aerosol concentration and size distribution for efficient inhaled lung drug delivery and is a potential atomization device for asthma treatment. Using the SAW device, we present comprehensive experimental results exploring the complexity of the acoustic atomization process and the influence of input power, device frequency, and liquid flow rate on aerosol size distribution. It is hoped that these studies will explain the mechanism of SAW atomization aerosol generation and how they can be controlled. The insights from the high-speed flow visualization studies reveal that it is possible by setting the input power above 4.17 W, thus allowing atomization to occur from a relatively thin film, forming dense, monodisperse aerosols. Moreover, we found that the aerosol droplet size can be effectively changed by adjusting the input power and liquid flow rate to change the film conditions. In this work, we proposed a method to realize drug atomization by a microfluidic channel. A SU-8 flow channel was prepared on the surface of a piezoelectric substrate by photolithography technology. Combined with the silicon dioxide coating process and PDMS process closed microfluidic channel was prepared, and continuous drug atomization was provided to improve the deposition efficiency of drug atomization by microfluidic.
引用
收藏
页数:17
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