A microfluidic device integrated with a stretchable microporous membrane controlled by electro-conjugate fluid

被引:1
|
作者
Otomo, Taiki [1 ]
Matsubara, Tatsuya [2 ]
Yoshida, Kazuhiro [3 ]
Kim, Deok-Ho [4 ]
Ikeuchi, Masashi [5 ]
Kim, Joon-wan [3 ]
机构
[1] Tokyo Inst Technol, Dept Mech Engn, J3-12, 4259 Nagatsuta cho, Midori ku, Yokohama 2268503, Japan
[2] Johns Hopkins Univ, Dept Biomed Engn, 3400 N Charles St, Baltimore, MD 21218 USA
[3] Tokyo Inst Technol, Inst Innovat Res IIR, Lab Future Interdisciplinary Res Sci & Technol FIR, J3-12, 4259 Nagatsuta cho, Midori ku, Yokohama 2268503, Japan
[4] Johns Hopkins Univ, Dept Med, Sch Med, 720 Rutland Ave, Baltimore, MD 21205 USA
[5] Tokyo Med & Dent Univ, Inst Biomat & Bioengn, Bldg 22, 2-3-10 Surugadai,Chiyoda ku, Tokyo, Japan
基金
日本学术振兴会;
关键词
Hydraulic power source; MEMS; Electro-conjugate fluid (ECF); Micropump; CHIP;
D O I
10.1016/j.sna.2023.114332
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Microfluidic devices that can apply stretch stimulation to cells to mimic the in vivo environment of organs have attracted significant attention as an alternative to animal testing in drug discovery screening. However, those devices reported in previous papers were driven by bulky fluid power systems composed of large external pumps and long tubing systems, which occupy much larger space than the main chip-based device itself and limit the number of simultaneous sample processing. Therefore, it is necessary to mount pressure sources on a single chip for miniaturizing the entire system. In this study, we propose to develop and mount MEMS-fabricated micro -pumps utilizing the strong flow of electro-conjugated fluid (ECF) into the microfluidic devices to stretch a microporous membrane, on which cultured cells can be simulated in various applications. The proposed microfluidic device is successfully fabricated, and its characteristics are investigated experimentally. The experimental results show that the device can stretch the microporous membrane with the strain (5-15%) at a frequency (0.2 Hz) similar to the organs' in vivo environment, demonstrating the feasibility of making the drug discovery screening efficient and effective.
引用
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页数:8
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